The DOI matches its Crossref record; 160 of the 162 references it cites were found in a registry or an index; 7 of the 184 sources its claims cite were checked for support.
An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH
Open accessAbstract
Successful development of treatments for non-alcoholic fatty liver disease and its progressive form, non-alcoholic steatohepatitis (NASH), has been challenging. Because NASH and fibrosis lead to progression towards cirrhosis and clinical outcomes, approaches have either sought to attenuate metabolic dysregulation and cell injury, or directly target the inflammation and fibrosis that ensue. Targets for reducing the activation of inflammatory cascades include nuclear receptor agonists (e.g. resmetirom, lanifibranor, obeticholic acid), modulators of lipotoxicity (e.g. aramchol, acetyl-CoA carboxylase inhibitors) or modification of genetic variants (e.g. PNPLA3 gene silencing). Extrahepatic inflammatory signals from the circulation, adipose tissue or gut are targets of hormonal agonists (semaglutide, tirzepatide, FGF19/FGF21 analogues), microbiota or lifestyle interventions. Stress signals and hepatocyte death activate immune responses, engaging innate (macrophages, innate lymphocyte populations) and adaptive (auto-aggressive T cells) mechanisms. Therapies have also been developed to blunt immune cell activation, recruitment (chemokine receptor inhibitors), and responses (e.g. galectin-3 inhibitors, anti-platelet drugs). The disease-driving pathways of NASH converge to elicit fibrosis, which is reversible. The activation of hepatic stellate cells into matrix-producing myofibroblasts can be inhibited by antagonising soluble factors (e.g. integrins, cytokines), cellular crosstalk (e.g. with macrophages), and agonising nuclear receptor signalling. In advanced fibrosis, cell therapy with restorative macrophages or reprogrammed (CAR) T cells may accelerate repair through hepatic stellate cell deactivation or killing, or by enhancing matrix degradation. Heterogeneity of disease - either due to genetics or divergent disease drivers - is an obstacle to defining effective drugs for all patients with NASH that will be overcome incrementally.
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Claims the paper makes
128 Not checked yet · 24 Own interpretation · 3 Supported · 2 No basis given · 1 Supported so far · 1 Partly supported · accuracy not yet measured
Every source the paper cites for this claim was checked and supports it.
In the paper
“Excessive energy substrates, especially carbohydrates, trigger hepatic de novo lipogenesis”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades
What the sources say
- Supportedcites [3] Loomba, 2021, Mechanisms and disease consequences of nonalcoholic fatty liver disease, Cell source
The ‘Metabolic mechanisms responsible for development of NAFLD’ section states that excess energy enters the liver largely as carbohydrates and fat, and that mono- and disaccharides can activate hepatic de novo lipogenesis. This supports the claim’s emphasis on carbohydrates. (LLM, conf=0.93)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Ultimately, those with NASH and fibrosis may develop end-stage complications such as cirrhosis, portal hypertension or hepatocellular carcinoma (HCC), which portend a much worse prognosis.6–10”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Supportedcites [6] Sanyal, 2021, Prospective study of outcomes in adults with nonalcoholic fatty liver disease, N Engl J Med source
The Discussion (page not supplied) links fibrosis to portal hypertension and reports higher rates of hepatic decompensation and hepatocellular carcinoma in patients with advanced fibrosis. It also reports increasing mortality with fibrosis stage and an association between hepatic decompensation and death, supporting the claim's worse-prognosis wording. (LLM, conf=0.92)
- Partly supportedcites [7] Simon, 2021, Mortality in biopsy-confirmed nonalcoholic fatty liver disease: results from a nationwide cohort, Gut sourceExperimental — accuracy not yet measured
The Introduction says NASH and fibrosis can lead to cirrhosis, decompensated liver disease, and death. The Results (Cause-Specific Mortality) report increasing cirrhosis- and HCC-related mortality with worsening NAFLD severity, supporting the poorer-prognosis point. Our copy does not identify portal hypertension as a complication or measure progression from NASH and fibrosis to HCC. (LLM, conf=0.86)
- Supportedcites [8] Vilar-Gomez, 2018, Fibrosis severity as a determinant of cause-specific mortality in patients with advanced nonalcoholic fatty liver disease: a multi-national cohort study, Gastroenterology source
The introductory passage (p. not available) describes progression from NASH to fibrosis, cirrhosis and liver failure. The Liver-Related Events section reports HCC and decompensation, including variceal bleeding; the Predictors of Overall Mortality and Major Clinical Outcomes section links cirrhosis to substantially worse survival. The paper also discusses portal hypertension in cirrhotic NASH, supporting the sentence’s broad description of advanced complications and poor prognosis. (LLM, conf=0.86)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
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- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Their enterohepatic circulation allows them to act as hormones by stimulating nuclear receptors such as FXR in the gut and liver,40”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Organ crosstalk in NAFLD: targeting extrahepatic inflammatory signals
What the sources say
- Supportedcites [40] Evangelakos, 2021, Role of bile acids in inflammatory liver diseases, Semin Immunopathol source
The Introduction states that bile acids exert hormone-like functions through activation of nuclear receptors including FXR. The section on enterohepatic circulation describes their movement from the intestine through the portal circulation to the liver, and the paper discusses intestinal and hepatic FXR signaling. Page numbers are unavailable in our copy. (LLM, conf=0.91)
plaindirect- Asserted: passes — The authors put it forward as true.
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- Supported
In the paper
“Among individuals with NASH, fibrosis progresses rapidly in some but relatively slowly in others.4”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Not checked yetcites [4] Singh, 2015, Fibrosis progression in nonalcoholic fatty liver vs nonalcoholic steatohepatitis: a systematic review and meta-analysis of paired-biopsy studies, Clin Gastroenterol Hepatol source
plain- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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None of the sources cited for this claim have been checked yet.
In the paper
“fibrosis stage is predictive of liver-specific morbidity and mortality.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Not checked yetcites [6] Sanyal, 2021, Prospective study of outcomes in adults with nonalcoholic fatty liver disease, N Engl J Med source
- Not checked yetcites [7] Simon, 2021, Mortality in biopsy-confirmed nonalcoholic fatty liver disease: results from a nationwide cohort, Gut source
- Not checked yetcites [8] Vilar-Gomez, 2018, Fibrosis severity as a determinant of cause-specific mortality in patients with advanced nonalcoholic fatty liver disease: a multi-national cohort study, Gastroenterology source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“dietary fat and the metabolically overwhelmed and dysfunctional adipose tissue provide excessive free fatty acids.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades
What the sources say
- Not checked yetcites [3] Loomba, 2021, Mechanisms and disease consequences of nonalcoholic fatty liver disease, Cell source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“Resolution of NASH back to NAFL can be highly dynamic and may occur even within a short time frame.5”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Not checked yetcites [5] Hagstrom, 2017, Fibrosis stage but not NASH predicts mortality and time to development of severe liver disease in biopsy-proven NAFLD, J Hepatol source
hedged- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
In the paper
“no drug is currently approved for the treatment of NASH.11”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Not checked yetcites [11] Ratziu, 2022, Breakthroughs in therapies for NASH and remaining challenges, J Hepatol source
plain- Asserted: passes — The authors put it forward as true.
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None of the sources cited for this claim have been checked yet.
In the paper
“Two key regulatory agencies, the FDA and EMA, have agreed that a substantial histological improvement, defined as resolution of NASH and/or improvement in fibrosis sinusoidal but can become panlobular as the disease stage, in sequential liver biopsies will be sufficient as a surrogate marker reasonably likely to yield drug approval and long-term benefit”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
- Not checked yetcites [12] Rinella, 2019, Report on the AASLD/EASL joint workshop on clinical trial endpoints in NAFLD, J Hepatol source
- Not checked yetcites [13] Loomba, 2022, Expert panel review to compare FDA and EMA guidance on drug development and endpoints in nonalcoholic steatohepatitis, Gastroenterology source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“indicating that targeting the genetic determinants of lipid handling in hepatocytes may also have (additional) antifibrotic effects through their impact on non-parenchymal cells.31”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Modulating hepatocytic cell metabolism and signalling to reduce inflammatory cascades
What the sources say
- Not checked yetcites [31] Carlsson, 2020, Review article: the emerging role of genetics in precision medicine for patients with non-alcoholic steatohepatitis, Aliment Pharmacol Ther source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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- It may state two separate claims as one. 65
- Probably not a substantial claim. 5
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Wound healing in the liver is dynamic and reversible,105 with ample evidence of fibrosis regression after effective treatment of viral hepatitis, and even following bariatric surgery in patients with NASH.106”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis
What the sources say
- Not checked yetcites [105] Kisseleva, 2021, Molecular and cellular mechanisms of liver fibrosis and its regression, Nat Rev Gastroenterol Hepatol source
- Supportedcites [106] Lassailly, 2020, Bariatric surgery provides long-term resolution of nonalcoholic steatohepatitis and regression of fibrosis, Gastroenterology source
The Discussion reports that fibrosis regressed in 70% of patients after long-term resolution of NASH following bariatric surgery. It also describes gradual improvement over five years. The citation supports the bariatric-surgery portion of the sentence; the viral-hepatitis statement is not the part attributed to this source. (LLM, conf=0.94)
boosteddirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“While belapectin’s safety and tolerability were good, belapectin did not improve clinically relevant endpoints including fibrosis regression.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting soluble mediators: inhibiting cytokines and other effector molecules
What the sources say
- Supportedcites [103] Chalasani, 2020, Effects of belapectin, an inhibitor of galectin-3, in patients with nonalcoholic steatohepatitis with cirrhosis and portal hypertension, Gastroenterology source
The paper’s phase 2b study of 162 patients found belapectin safe and well tolerated, with no significant overall reduction in HVPG or fibrosis versus placebo (Conclusions). The Discussion likewise reports no significant changes in liver histology or cirrhosis complications, while noting a benefit in a subgroup without baseline varices. (LLM, conf=0.92)
plainn = 162- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Supported
In the paper
“lipotoxicity – defined as the generation of injurious lipid metabolites – is a key feature of progressive NAFLD, involving production of reactive oxygen species, mitochondrial dysfunction and the development of endoplasmic reticulum stress.3”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades
What the sources say
- Not checked yetcites [3] Loomba, 2021, Mechanisms and disease consequences of nonalcoholic fatty liver disease, Cell source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The natural course of NAFLD is heterogeneous, with substantial inter-patient variability, which is influenced by several non-modifiable (age, sex, race/ethnicity, family history, genetics) and modifiable (lifestyle/diet/exercise, comorbidities, drugs, alcohol) risk factors.2,3”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Because fibrosis is the most compelling predictor of outcomes, current and future therapies must improve fibrosis”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Introduction
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: fails — It may be too vague to check against evidence.
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Probably not a substantial claim. It may be too vague to check against evidence. The paper may give no reason why it holds.
In the paper
“Structurally engineered fatty acids, such as icosabutate, improve resistance to peroxidative processes, and thus represent a promising approach to maintaining the beneficial metabolic effects of long-chain omega-3 fatty acids.15”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Modulating hepatocytic cell metabolism and signalling to reduce inflammatory cascades
What the sources say
- Not checked yetcites [15] Fraser, 2022, A structurally engineered fatty acid, icosabutate, suppresses liver inflammation and fibrosis in NASH, J Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
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It may state two separate claims as one.
In the paper
“Long-chain omega-3 fatty acids are known to beneficially regulate inflammatory pathways in the course of NASH, but therapeutic efficacy is highly limited by peroxidation and subsequent degradation.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Modulating hepatocytic cell metabolism and signalling to reduce inflammatory cascades
What the sources say
- Not checked yetcites [15] Fraser, 2022, A structurally engineered fatty acid, icosabutate, suppresses liver inflammation and fibrosis in NASH, J Hepatol source
boosteddirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“For instance, bile acids are soluble mediators and key components of the gut-liver axis, connecting altered intestinal homeostasis (e.g. dysbiosis, increased permeability) to metabolic injury in NAFLD.35”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Organ crosstalk in NAFLD: targeting extrahepatic inflammatory signals
What the sources say
- Not checked yetcites [35] Tilg, 2022, Gut-liver axis: pathophysiological concepts and clinical implications, Cel Metab source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“Ample preclinical evidence supports microbiota interventions to reduce NAFLD-related liver inflammation; however, evidence for long-term anti-inflammatory or antifibrotic effects in clinical trials is lacking.43”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Organ crosstalk in NAFLD: targeting extrahepatic inflammatory signals
What the sources say
- Not checked yetcites [43] Albillos, 2020, The gut-liver axis in liver disease: pathophysiological basis for therapy, J Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Conceptually, reversing gut dysbiosis in NAFLD using pre-/pro-/antibiotics or faecal microbiota transplantation would reduce these inflammatory signals, reverse perturbations in gut barrier function (thereby further reducing endotoxin in the portal vein) and promote the endogenous production of beneficial mediators (FGFs, GLP-1, secondary bile acids).”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From metabolic injury to inflammation: Targeting the activation of inflammatory cascades > Organ crosstalk in NAFLD: targeting extrahepatic inflammatory signals
hedgeddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Liver macrophages are key to the pathogenesis of NAFLD (Fig. 2), as they accumulate with disease progression in human biopsies.50–52”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
What the sources say
- Not checked yetcites [50] Guillot, 2023, Mapping the hepatic immune landscape identifies monocytic macrophages as key drivers of steatohepatitis and cholangiopathy progression, Hepatology source
- Not checked yetcites [51] Kazankov, 2019, The role of macrophages in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis, Nat Rev Gastroenterol Hepatol source
- Not checked yetcites [52] Wen, 2021, Hepatic macrophages in liver homeostasis and diseases-diversity, plasticity and therapeutic opportunities, Cell Mol Immunol source
plaindirect- Asserted: passes — The authors put it forward as true.
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None of the sources cited for this claim have been checked yet.
In the paper
“When Kupffer cells sense hepatocyte stress and injury signals from other cells (or extrahepatic sources), they activate inflammatory signals, recruit monocytes (and other inflammatory cells) via chemokines and engulf cellular debris.53,54”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“For instance, activation of TLR4 via LPS leads to the release of pro-inflammatory cytokines (e.g., TNF, interleukin [IL]-6), but similar effects are also observed if free fatty acids bind to TLR4.63”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
What the sources say
- Not checked yetcites [63] Shi, 2006, TLR4 links innate immunity and fatty acid-induced insulin resistance, J Clin Invest source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Kupffer cells comprise subsets/differentiation states, of which the CD206hi ESAM+ subtype (in mice) participates in fatty acid metabolism and may thereby directly drive NASH.56”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
What the sources say
- Not checked yetcites [56] Bleriot, 2021, A subset of Kupffer cells regulates metabolism through the expression of CD36, Immunity source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Still, it is likely that immune subsets are more complex and nuanced than we currently understand in their functions during NASH.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk
hedged- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. It may be too vague to check against evidence. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Given the opposing distribution of NKT cells and MAIT cells between human and mouse livers, findings about NKT cells from rodent models need to be interpreted with caution, and, from a functional perspective, MAIT cells may be the human counterpart of NKT cells.39,98”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
hedgedconditional- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“In NASH, XCR1 (X–C motif chemokine receptor 1)-expressing cDC1s are found abundantly in both patients with NASH and murine steatohepatitis, and correlate with NASH severity.85”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
- Not checked yetcites [85] Deczkowska, 2021, XCR1(+) type 1 conventional dendritic cells drive liver pathology in non-alcoholic steatohepatitis, Nat Med source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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In the paper
“While many of these discoveries have been based on mouse models, scRNA-seq analyses from human livers have also identified SAMs as a unique population located in the fibrotic niche of cirrhotic livers of different disease aetiologies.74”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting immune cell recruitment: chemokine and chemokine receptor inhibition
What the sources say
- Not checked yetcites [74] Ramachandran, 2019, Resolving the fibrotic niche of human liver cirrhosis at single-cell level, Nature source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“However, similar to the concern about using classical immunosuppressant drugs as highlighted above, their use in NAFLD is currently constrained by the lack of clinical data indicating beneficial effects on NASH and/or fibrosis, as well as their unfavourable safety profiles.79”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting soluble mediators: inhibiting cytokines and other effector molecules
What the sources say
- Not checked yetcites [79] Wiering, 2023, Treating inflammation to combat non-alcoholic fatty liver disease, J Endocrinol
plain- Asserted: passes — The authors put it forward as true.
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- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
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It may state two separate claims as one.
In the paper
“For instance, platelets bind to hepatic macrophages, and their activation further aggravates inflammation.80”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
- Not checked yetcites [80] Malehmir, 2019, Platelet GPIbalpha is a mediator and potential interventional target for NASH and subsequent liver cancer, Nat Med source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“These infiltrating monocyte-derived macrophages can promote both fibrogenesis71 and fibrosis resolution.72,73”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting immune cell recruitment: chemokine and chemokine receptor inhibition
What the sources say
- Not checked yetcites [71] Krenkel, 2018, Therapeutic inhibition of inflammatory monocyte recruitment reduces steatohepatitis and liver fibrosis, Hepatology source
- Not checked yetcites [72] Pellicoro, 2014, Liver fibrosis and repair: immune regulation of wound healing in a solid organ, Nat Rev Immunol source
- Not checked yetcites [73] Baeck, 2014, Pharmacological inhibition of the chemokine C-C motif chemokine ligand 2 (monocyte chemoattractant protein 1) accelerates liver fibrosis regression by suppressing Ly-6C(+) macrophage infiltration in mice, Hepatology source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“C–C motif chemokine receptor (CCR)2+ monocytes are important drivers of liver inflammation in NASH, and their therapeutic inhibition reduces NASH and fibrosis in rodent models.71,76”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting immune cell recruitment: chemokine and chemokine receptor inhibition
What the sources say
- Not checked yetcites [71] Krenkel, 2018, Therapeutic inhibition of inflammatory monocyte recruitment reduces steatohepatitis and liver fibrosis, Hepatology source
- Not checked yetcites [76] Krenkel, 2017, Macrophages in nonalcoholic fatty liver disease: a role model of pathogenic immunometabolism, Semin Liver Dis source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“More recently, a population of CXCR6+ Granzyme+ PD1+ CD8+ T cells was identified in NASH livers, which are directly activated by metabolic stimuli (including acetate and extracellular ATP) and collectively triggered auto-aggression against hepatocytes, in an antigen-independent fashion.87”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
- Not checked yetcites [87] Dudek, 2021, Auto-aggressive CXCR6(+) CD8 T cells cause liver immune pathology in NASH, Nature source
plaindirect- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Because inhibiting inflammatory signalling in macrophages is therapeutically challenging in NASH, augmenting anti-inflammatory signalling via targets that promote disease resolution may be the more realistic approach.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
hedgedconditional- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Long-term risk of infection, specific side effects such as weight gain, and the lack of antigen-specific autoimmunity in NASH all argue against their use in the disease.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In NAFLD and NASH, the NLR family pyrin domain containing 3 (NLRP3) inflammasome has been identified as a central driver of inflammation – via activation of caspase 1 and the release of inflammatory cytokines (e.g., IL-1β) – and as an inducer of inflammatory (“pyroptotic”) cell death.64”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
What the sources say
- Not checked yetcites [64] Knorr, 2020, The NLRP3 inflammasome in alcoholic and nonalcoholic steatohepatitis, Semin Liver Dis source
plaindirect- Asserted: passes — The authors put it forward as true.
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A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These innate and unconventional immune cell populations are affected by interventions on the gut-liver axis and could represent promising targets for future NASH therapies as well.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“NKT cells are much more abundant in mouse livers than in humans, and they promote NASH, fibrosis and carcinogenesis in experimental models.86,96,97”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
- Not checked yetcites [86] Wolf, 2014, Metabolic activation of intrahepatic CD8+ T cells and NKT cells causes nonalcoholic steatohepatitis and liver cancer via cross-talk with hepatocytes, Cancer Cell source
- Not checked yetcites [96] Syn, 2012, NKT-associated hedgehog and osteopontin drive fibrogenesis in non-alcoholic fatty liver disease, Gut source
- Not checked yetcites [97] Wehr, 2013, Chemokine receptor CXCR6-dependent hepatic NK T Cell accumulation promotes inflammation and liver fibrosis, J Immunol source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“However, despite favourable tolerability as well as antifibrotic efficacy after 1 year of treatment in adults with NASH and liver fibrosis in a phase II trial,78 cenicriviroc did not demonstrate sustained antifibrotic efficacy after 1 year of treatment in a larger phase III clinical trial following interim analysis, leading to the termination of its development as a monotherapy in NASH.79”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting immune cell recruitment: chemokine and chemokine receptor inhibition
What the sources say
- Not checked yetcites [78] Ratziu, 2020, Cenicriviroc treatment for adults with nonalcoholic steatohepatitis and fibrosis: final analysis of the phase 2b CENTAUR study, Hepatology source
- Not checked yetcites [79] Wiering, 2023, Treating inflammation to combat non-alcoholic fatty liver disease, J Endocrinol
boosteddirect- Asserted: passes — The authors put it forward as true.
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In the paper
“For instance, NK cells are considered anti-fibrogenic due to their capacity to eliminate HSCs,91 but they may also support hepatic inflammation and alter metabolism.92”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Of note, ILC1, ILC2 and ILC3 populations have been implicated in metabolic disorders beyond NAFLD (e.g. obesity).93,94”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
plaincorrelational- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Based on proteo-genomic data combined with spatial information, LAMs (SAMs) locate near intrahepatic bile ducts in homeostasis, but shift towards steatotic areas, fostered by increased C–C motif chemokine ligand 2 (CCL2) expression by HSCs.75”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting immune cell recruitment: chemokine and chemokine receptor inhibition
What the sources say
- Not checked yetcites [75] Guilliams, 2022, Spatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage niches, Cell source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Neutrophils are also abundant in NASH livers, particularly in early stages, and may contribute to inflammation by releasing toxic molecules including proteases, oxidants, cytokines and NETs (neutrophil extracellular traps).81”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Modulating immune cell crosstalk: targeting platelets, neutrophils and lymphocytes
What the sources say
- Not checked yetcites [81] Jorch, 2017, An emerging role for neutrophil extracellular traps in noninfectious disease, Nat Med source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“In addition, quiescent and activated HSCs are transcriptomically distinct in human livers, with activated HSCs downregulating vitamin A storage-related genes and upregulating profibrogenic genes such as collagen I.113”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting signals promoting HSC activation: TGF-β and integrin inhibitors
What the sources say
- Not checked yetcites [113] MacParland, 2018, Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations, Nat Commun source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“HSC activation into myofibroblasts requires energy, so that HSC activation necessitates an intense metabolic reprogramming through activation of glycolysis, glutaminolysis (using glutamine as an additional source of ATP), and lipogenesis.70”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [70] Gilgenkrantz, 2021, Targeting cell-intrinsic metabolism for antifibrotic therapy, J Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Moreover, the evolution of a dense autocrine network indicates that as fibrosis advances, the repertoire of therapeutic targets evolves, so that treatments for early disease may be less effective in advanced fibrosis.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting signals promoting HSC activation: TGF-β and integrin inhibitors
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Intracellular lipids released during autophagy act as an additional energy source for HSC activation, revealing another therapeutic vulnerability that could be targeted by antifibrotic strategies.122”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [122] Hernandez-Gea, 2012, Autophagy releases lipid that promotes fibrogenesis by activated hepatic stellate cells in mice and in human tissues, Gastroenterology source
hedgeddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Most recently, the fatty acid synthase inhibitor denifanstat (TVB-2640) also demonstrated antifibrotic activity in HSCs while improving NASH.121”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [121] O'Farrell, 2022, FASN inhibition targets multiple drivers of NASH by reducing steatosis, inflammation and fibrosis in preclinical models, Sci Rep
boosteddirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“As noted above, autophagy (i.e. the lysosome-dependent orderly degradation and recycling of cellular components) may generate energy during HSC activation,127 such that inhibiting autophagy would be antifibrotic.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [127] Thoen, 2011, A role for autophagy during hepatic stellate cell activation, J Hepatol source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The acetyl-CoA carboxylase inhibitors firsocostat, as well as clesacostat (PF-05221304), both reduced liver fibrosis in animal models, independently of their anti-steatotic effects, and HSC activation in vitro.117,118”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [117] Bates, 2020, Acetyl-CoA carboxylase inhibition disrupts metabolic reprogramming during hepatic stellate cell activation, J Hepatol source
- Not checked yetcites [118] Ross, 2020, Acetyl-CoA carboxylase inhibition improves multiple dimensions of NASH pathogenesis in model systems, Cell Mol Gastroenterol Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Targeting TGF-β directly with antibodies (e.g., fresolimumab or metelimumab) has been largely terminated due to dose-limiting adverse events, since systemic inhibition of the cytokine is immunosuppressive and may promote cancer.114”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting signals promoting HSC activation: TGF-β and integrin inhibitors
What the sources say
- Not checked yetcites [114] Henderson, 2020, Fibrosis: from mechanisms to medicines, Nature source
plainconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“HSCs express several nuclear receptors that a retargets of investigational drugs for NASH, including low levels of FXR, high levels of LXR, robust levels of THR-α (but low levels of THR-β) and different isoforms of PPARs.129”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [129] Konigshofer, 2021, Nuclear receptors in liver fibrosis, Biochim Biophys Acta Mol Basis Dis source
plain- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“During HSC transdifferentiation to myofibroblasts in vitro, glucose transporters (e.g., glucose transporter 1) and glycolytic enzymes (e.g., hexokinase 2) are induced, and gluconeogenesis is downregulated.70”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [70] Gilgenkrantz, 2021, Targeting cell-intrinsic metabolism for antifibrotic therapy, J Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: passes — The paper’s conclusions depend on it.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, hexokinase inhibitors (e.g., PF-06835919) or SGLT2 (sodium glucose linked transporter 2) inhibitors like empaglifozin, licoglifozin or dapaglifozin may attenuate HSC activation and fibrogenesis.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“The selective inhibition of stearoyl-CoA desaturase 1 in HSCs reduced their activation and inhibited fibrosis in rodent models.120”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [120] Lai, 2017, Stearoyl-CoA desaturase promotes liver fibrosis and tumor development in mice via a wnt positive-signaling loop by stabilization of low-density lipoprotein-receptor-related proteins 5 and 6, Gastroenterology source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Similar to cytokines, galectin 3 is secreted by macrophages upon liver injury in NASH and has profibrotic activity.102”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting soluble mediators: inhibiting cytokines and other effector molecules
What the sources say
- Not checked yetcites [102] Al Attar, 2021, Review of galectin-3 inhibitors in the treatment of nonalcoholic steatohepatitis, Expert Rev Clin Pharmacol source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“HSC activation in NASH is mainly driven by: i) soluble signals such as platelet-derived growth factor (PDGF), vascular endothelial growth factor, and transforming growth factor (TGF)-β; ii) by paracrine interactions with macrophages and other immune cells, as well as hepatocytes and endothelial cells; it is also accompanied by metabolic reprogramming.70,108”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting signals promoting HSC activation: TGF-β and integrin inhibitors
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“The disease-driving pathways of NASH converge in fibrosis (Fig. 3), an aberrant wound-healing process resulting not only in scarring (extracellular matrix deposition), but also in the loss of functional hepatocytes and chronic inflammation.104”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis
What the sources say
- Not checked yetcites [104] Schwabe, 2020, Mechanisms of fibrosis development in nonalcoholic steatohepatitis, Gastroenterology source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“Nonetheless, one important lesson from alcohol-associated hepatitis is that the broad application of steroids, anakinra (recombinant IL-1 receptor antagonist), pentoxifyllin (which inhibits TNF synthesis) or infliximab (anti-TNF antibody) does not provide benefit, and may aggravate this inflammatory condition.101”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting soluble mediators: inhibiting cytokines and other effector molecules
What the sources say
- Not checked yetcites [101] Bataller, 2022, Alcohol-associated hepatitis, N Engl J Med source
plainconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“However, proper macrophage differentiation is probably required, because mouse models of fibrosis have demonstrated that the adoptive transfer of “non-programmed” immature bone marrow monocytes aggravates liver fibrosis, while the intravenous administration of properly (ex vivo) differentiated macrophages ameliorates hepatic fibrosis.149,150”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
What the sources say
- Not checked yetcites [149] Thomas, 2011, Macrophage therapy for murine liver fibrosis recruits host effector cells improving fibrosis, regeneration, and function, Hepatology source
- Not checked yetcites [150] Ma, 2017, Cytotherapy with M1-polarized macrophages ameliorates liver fibrosis by modulating immune microenvironment in mice, J Hepatol source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Nonetheless, the clinical efficacy of this approach is unknown, and many questions remain unanswered, including the efficiency of engraftment, cell viability, phenotype stability, and whether macrophages are the optimal cell for this purpose.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
plainn = 9- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Since HSCs/myofibroblasts, matrix proteins and fibrolytic pathways are challenging therapeutic targets, cell-based therapies are being explored to augment anti-inflammatory and antifibrotic activity.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
In the paper
“While MSC transfer led to promising antifibrotic effects in mouse models, clinical trials on MSCs in humans have yielded mixed results.145”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
What the sources say
- Not checked yetcites [145] Dwyer, 2021, Cell therapy for advanced liver diseases: repair or rebuild, J Hepatol source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“In this proof-of-concept trial, apheresis-derived autologous CD14+ monocytes were differentiated ex vivo into a restorative phenotype (CD14+, high 25F9, CD206, CD163 and CD169). The single injection of different doses of these macrophages appeared safe and was associated with a (slight) reduction in the model of end-stage liver disease score.151”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
What the sources say
- Not checked yetcites [151] Moroni, 2019, Safety profile of autologous macrophage therapy for liver cirrhosis, Nat Med source
hedgedcorrelationaln = 9- Asserted: passes — The authors put it forward as true.
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In the paper
“Consistently, clinical data with obeticholic acid reported an improvement of liver fibrosis in non-cirrhotic NASH,132 but not in patients with compensated cirrhosis.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Targeting HSC activation: lipid metabolism, autophagy and nuclear receptors
What the sources say
- Not checked yetcites [132] Younossi, 2019, Obeticholic acid for the treatment of non-alcoholic steatohepatitis: interim analysis from a multicentre, randomised, placebo-controlled phase 3 trial, Lancet source
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The mechanisms underlying disease regression are less well understood, but several molecular and cellular principles have been identified based on mouse models24 as well as samples from patients with NASH following disease regression, for example after bariatric surgery or lifestyle modifications.137”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression
What the sources say
- Not checked yetcites [24] Peiseler, 2022, Immune mechanisms linking metabolic injury to inflammation and fibrosis in fatty liver disease - novel insights into cellular communication circuits, J Hepatol source
- Not checked yetcites [137] Haas, 2019, Transcriptional network analysis implicates altered hepatic immune function in NASH development and resolution, Nat Metab source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Macrophages can adopt a repair phenotype that promotes fibrosis regression and proper tissue regeneration, supporting the concept of programmed macrophage transplantation as a therapeutic strategy (Fig. 2).”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
plaindirectn = 9- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Hepatic fibrosis is dynamic and reversible prior to the development of cirrhosis, and even cirrhosis may be reversible if not too advanced; however, specific features of advanced liver disease such as capillarisation of the liver sinusoids might be less reversible.105”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression
What the sources say
- Not checked yetcites [105] Kisseleva, 2021, Molecular and cellular mechanisms of liver fibrosis and its regression, Nat Rev Gastroenterol Hepatol source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, despite the relevance of inflammation and fibrosis to NAFLD-related outcomes, no “pure” anti-inflammatory or antifibrotic compound has been approved for the treatment of NASH. This is likely related to the complexity of the processes driving inflammation and fibrosis, but also to redundancy in inflammatory and fibrogenic signalling.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Challenges in translation from anti-inflammatory/antifibrotic target identification to drug approval
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Rests on an assumption: No pure anti-inflammatory or antifibrotic compound has been approved for NASH.
In the paper
“Currently, a retinoid-conjugated lipid nanoparticle containing small-interfering RNA against heat-shock protein 47 (HSP47, BMS-986263) is being tested in a phase II clinical trial for patients with compensated NASH cirrhosis, since it demonstrated favourable safety and some efficacy in patients regressing from hepatitis C virus-associated fibrosis.135”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Nanoparticle-mediated drug delivery to HSCs: gene silencing or activation
What the sources say
- Not checked yetcites [135] Lawitz, 2022, BMS-986263 in patients with advanced hepatic fibrosis: 36-week results from a randomized, placebo-controlled phase 2 trial, Hepatology source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Since MSCs appear to exert many of their beneficial actions via the release of extracellular vesicles, the use of MSC-derived extracellular vesicles instead of cells could be an interesting cell-free, less immunogenic, and less toxic alternative antifibrotic strategy.155”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
What the sources say
- Not checked yetcites [155] Psaraki, 2022, Extracellular vesicles derived from mesenchymal stem/stromal cells: the regenerative impact in liver diseases, Hepatology source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Nonetheless, the clinical translation of this approach is challenging because uPAR is not only expressed on senescent cells, but also on several immune cell populations including neutrophils and macrophages, and cellular senescence has cell type-dependent functions in fibrosis that may undermine efforts to deplete senescent cells as a therapy.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“On the other hand, other efforts to target fibrogenic cells in the heart by targeting cell surface FAP-1 (fibroblast activating protein) are very encouraging, and may be adaptable to liver disease.147,148”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
What the sources say
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Moreover, targeting critical downstream pathways of inflammation and fibrosis, for example by depleting immune cells or antagonising cytokines, carries a high risk of undermining important immune surveillance functions,158 making such approaches unacceptably risky for a chronic condition such as NASH.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Challenges in translation from anti-inflammatory/antifibrotic target identification to drug approval
What the sources say
- Not checked yetcites [158] Jenne, 2013, Immune surveillance by the liver, Nat Immunol source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“iii) deactivation or elimination of myofibroblasts by reverting them to a quiescent HSC-like phenotype, via HSC senescence or by elimination of activated HSCs via NK cells or T cells 91,105,141;”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression
What the sources say
- Not checked yetcites [91] Gur, 2012, NKp46-mediated killing of human and mouse hepatic stellate cells attenuates liver fibrosis, Gut source
- Not checked yetcites [105] Kisseleva, 2021, Molecular and cellular mechanisms of liver fibrosis and its regression, Nat Rev Gastroenterol Hepatol source
- Not checked yetcites [141] Koda, 2021, CD8(+) tissue-resident memory T cells promote liver fibrosis resolution by inducing apoptosis of hepatic stellate cells, Nat Commun source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Regardless, efficient cytotherapy will require long-term stability of a “repair macrophage” phenotype.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression > Cell therapy-based anti-inflammatory and antifibrotic approaches
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper may give no reason why it holds.
In the paper
“However, HSC specificity is critical as some “HSC-specific nanoparticles” target macrophages, possibly through their phagocytic capacity.136”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > From inflammation to fibrosis: Targeting fibrogenesis > Nanoparticle-mediated drug delivery to HSCs: gene silencing or activation
What the sources say
- Not checked yetcites [136] Ergen, 2019, Liver fibrosis affects the targeting properties of drug delivery systems to macrophage subsets in vivo, Biomaterials source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“This would, however, support the concept of combinatorial treatment for NASH, as combining anti-inflammatory strategies could amplify the efficacy of metabolic drugs and overcome signalling redundancies.156”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Challenges in translation from anti-inflammatory/antifibrotic target identification to drug approval
What the sources say
- Not checked yetcites [156] Ratziu, 2023, Rational combination therapy for NASH: insights from clinical trials and error, J Hepatol source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Full matrix degradation also requires reduced levels of MMP-inhibitory proteins (e.g. TIMP [tissue inhibitor of MMP]) and the presence of phagocytic macrophages.142”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Augmenting scar-free tissue repair and regeneration: Targeting fibrosis regression
What the sources say
- Not checked yetcites [142] Caligiuri, 2021, Cellular and molecular mechanisms underlying liver fibrosis regression, Cells
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper relies on this without support.
Inflammation and fibrosis are evolutionarily conserved endogenous defence mechanisms.
“However, inflammation and fibrosis represent evolutionarily conserved, endogenous defence mechanisms, so that targets for intervention must be selected carefully”
The paper relies on this without support.
The gut and liver form an anatomically and functionally linked unit, the gut-liver axis.
“since the gut and liver form an anatomically and functionally linked unit, the “gut-liver axis”.”
The paper relies on this without support.
Many harmful effects of NASH inflammation, including hepatocyte death and activation of fibrogenic myofibroblasts, are mediated by soluble factors.
“Many of the detrimental effects of inflammation in NASH – including death of hepatocytes and activation of fibrogenic myofibroblast populations – are mediated by soluble factors.”
The paper relies on this without support.
The body has evolved many overlapping mechanisms that preserve inflammation and fibrogenesis for tissue homeostasis or damage control.
“In order to ensure tissue homeostasis or – in the case of injury – damage control, the body has evolved many overlapping mechanisms to preserve inflammation and fibrogenesis.”
The paper relies on this without support.
Many cellular components of liver fibrosis can adapt their phenotypes to the hepatic microenvironment.
“In fact, many cellular components of liver fibrosis show a tremendous capacity to adapt their phenotypes towards the hepatic microenvironment, making it challenging to treat the disease if the tissue injury is ongoing.”
The paper relies on this without support.
No pure anti-inflammatory or antifibrotic compound has been approved for NASH.
“However, despite the relevance of inflammation and fibrosis to NAFLD-related outcomes, no “pure” anti-inflammatory or antifibrotic compound has been approved for the treatment of NASH.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
“Several strategies therefore aim to block danger recognition on macrophages and other cells, for example by inhibiting TLR4 via serelaxin or TAK-242, or through activation of the inflammasome, a multiprotein intracellular complex.”
§ An integrated view of anti-inflammatory and antifibrotic targets for the treatment of NASH > Establishing inflammation in NAFLD: Targeting immune cell activation, recruitment and cellular crosstalk > Targeting the activation of inflammation: inhibition of TLRs, inflammasome or inflammatory signalling
“Pharmacological inhibition of NLRP3 activation has been proposed for a wide range of inflammatory diseases,65 but is currently still in early-stage development for NASH.”
Citations
Cites
TLR4 links innate immunity and fatty acid-induced insulin resistance
Shi, H., Kokoeva, M. V., Inouye, K., Tzameli, I., Yin, H., & Flier, J. S. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28898 · Cited by 3,690
Younossi, Z. M., Golabi, P., Paik, J. M., Henry, A., Van Dongen, C., & Henry, L. (2023) · Hepatology · doi:10.1097/hep.0000000000000004 · Cited by 3,383
Mechanisms of hepatic stellate cell activation
Tsuchida, T., & Friedman, S. L. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.38 · Cited by 2,909
Self-citationNon-alcoholic fatty liver disease
Powell, E. E., Wong, V. W.-S., & Rinella, M. (2021) · The Lancet · doi:10.1016/s0140-6736(20)32511-3 · Cited by 2,789
The gut-liver axis in liver disease: Pathophysiological basis for therapy
Albillos, A., de Gottardi, A., & Rescigno, M. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2019.10.003 · Cited by 2,166
Innate Lymphoid Cells: 10 Years On
Vivier, É., Artis, D., Colonna, M., Diefenbach, A., Santo, J. P. D., Eberl, G., Koyasu, S., Locksley, R. M., McKenzie, A. N. J., Mebius, R. E., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.017 · Cited by 2,136
A Placebo-controlled trial of subcutaneous semaglutide in nonalcoholic steatohepatitis
Newsome, P. N., Buchholtz, K., Cusi, K., Linder, M., Okanoue, T., Ratziu, V., Sanyal, A. J., Sejling, A.-S., & Harrison, S. A. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2028395 · Cited by 2,039
Molecular and cellular mechanisms of liver fibrosis and its regression
Kisseleva, T., & Brenner, D. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00372-7 · Cited by 2,024
Mechanisms and disease consequences of nonalcoholic fatty liver disease
Loomba, R., Friedman, S. L., & Shulman, G. I. (2021) · Cell · doi:10.1016/j.cell.2021.04.015 · Cited by 2,002
Self-citationDulai, P. S., Singh, S., Patel, J., Soni, M., Prokop, L. J., Younossi, Z., Sebastiani, G., Ekstedt, M., Hagstrom, H., Nasr, P., et al. (2017) · Hepatology · doi:10.1002/hep.29085 · Cited by 1,965
Self-citationTargeting the NLRP3 inflammasome in inflammatory diseases
Mangan, M. S. J., Olhava, E. J., Roush, W. R., Seidel, H. M., Glick, G. D., & Latz, E. (2018) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2018.97 · Cited by 1,885
Fibrosis: from mechanisms to medicines
Henderson, N. C., Rieder, F., & Wynn, T. A. (2020) · Nature · doi:10.1038/s41586-020-2938-9 · Cited by 1,868
Resolving the fibrotic niche of human liver cirrhosis at single-cell level
Ramachandran, P., Dobie, R., Wilson-Kanamori, J. R., Dora, E. F., Henderson, B. E. P., Luu, N. T., Portman, J. R., Matchett, K. P., Brice, M., Marwick, J. A., et al. (2019) · Nature · doi:10.1038/s41586-019-1631-3 · Cited by 1,784
Self-citationSingh, S., Allen, A. M., Wang, Z., Prokop, L. J., Murad, M. H., & Loomba, R. (2015) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2014.04.014 · Cited by 1,748
Self-citationSingle cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations
MacParland, S. A., Liu, J. C., Ma, X.-Z., Innes, B. T., Bartczak, A. M., Gage, B. K., Manuel, J., Khuu, N., Echeverri, J., Linares, I., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06318-7 · Cited by 1,552
Liver Macrophages in Tissue Homeostasis and Disease
Krenkel, O., & Tacke, F. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.11 · Cited by 1,424
Self-citationCAR T cells produced in vivo to treat cardiac injury
Rurik, J. G., Tombácz, I., Yadegari, A., Méndez Fernández, P. O., Shewale, S. V., Li, L., Kimura, T., Soliman, O. Y., Papp, T. E., Tam, Y. K., et al. (2022) · Science · doi:10.1126/science.abm0594 · Cited by 1,400
Lipid-associated macrophages control metabolic homeostasis in a Trem2-dependent manner
Jaitin, D. A., Adlung, L., Thaiss, C. A., Weiner, A., Li, B., Descamps, H., Lundgren, P., Bleriot, C., Liu, Z., Deczkowska, A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.05.054 · Cited by 1,377
Resolvins in inflammation: emergence of the pro-resolving superfamily of mediators
Serhan, C. N., & Levy, B. D. (2018) · Journal of Clinical Investigation · doi:10.1172/jci97943 · Cited by 1,344
Liver fibrosis and repair: Immune regulation of wound healing in a solid organ
Pellicoro, A., Ramachandran, P., Iredale, J. P., & Fallowfield, J. A. (2014) · Nature Reviews Immunology · doi:10.1038/nri3623 · Cited by 1,310
Younossi, Z. M., Ratziu, V., Loomba, R., Rinella, M., Anstee, Q. M., Goodman, Z., Bedossa, P., Geier, A., Beckebaum, S., Newsome, P. N., et al. (2019) · The Lancet · doi:10.1016/s0140-6736(19)33041-7 · Cited by 1,277
Self-citationAn emerging role for neutrophil extracellular traps in noninfectious disease
Jorch, S. K., & Kubes, P. (2017) · Nature Medicine · doi:10.1038/nm.4294 · Cited by 1,244
Immunology in the liver — from homeostasis to disease
Heymann, F., & Tacke, F. (2016) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.200 · Cited by 1,180
Self-citationProspective Study of Outcomes in Adults with Nonalcoholic Fatty Liver Disease
Sanyal, A. J., Van Natta, M. L., Clark, J., Neuschwander-Tetri, B. A., Diehl, A., Dasarathy, S., Loomba, R., Chalasani, N., Kowdley, K., Hameed, B., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2029349 · Cited by 1,146
Self-citationSenolytic CAR T cells reverse senescence-associated pathologies
Amor, C., Feucht, J., Leibold, J., Ho, Y.-J., Zhu, C., Alonso-Curbelo, D., Mansilla-Soto, J., Boyer, J. A., Li, X., Giavridis, T., et al. (2020) · Nature · doi:10.1038/s41586-020-2403-9 · Cited by 1,098
Self-citationHagström, H., Nasr, P., Ekstedt, M., Hammar, U., Stål, P., Hultcrantz, R., & Kechagias, S. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.07.027 · Cited by 1,067
Immune surveillance by the liver
Jenne, C. N., & Kubes, P. (2013) · Nature Immunology · doi:10.1038/ni.2691 · Cited by 1,047
Targeting hepatic macrophages to treat liver diseases
Tacke, F. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.02.026 · Cited by 1,003
Self-citationSpatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage niches
Guilliams, M., Bonnardel, J., Haest, B., Vanderborght, B., Wagner, C., Remmerie, A., Bujko, A., Martens, L., Thoné, T., Browaeys, R., et al. (2022) · Cell · doi:10.1016/j.cell.2021.12.018 · Cited by 985
Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity
Brestoff, J. R., Kim, B. S., Saenz, S. A., Stine, R. R., Monticelli, L. A., Sonnenberg, G. F., Thome, J. J., Farber, D. L., Lutfy, K., Seale, P., et al. (2015) · Nature · doi:10.1038/nature14115 · Cited by 968
The role of macrophages in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis
Kazankov, K., Jørgensen, S. M. D., Thomsen, K. L., Møller, H. J., Vilstrup, H., George, J., Schuppan, D., & Grønbæk, H. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0082-x · Cited by 941
CAR T Cells Produced in vivo to Treat Cardiac Injury
Rurik, J. G., Tombácz, I., Yadegari, A., Fernández, P. O. M., Shewale, S. V., Li, L., Kimura, T., Soliman, O. Y., Papp, T. E., Tam, Y. K., et al. (2023) · HAL · Cited by 926
Henderson, N. C., Arnold, T. D., Katamura, Y., Giacomini, M. M., Rodriguez, J. D., McCarty, J. H., Pellicoro, A., Raschperger, E., Betsholtz, C., Ruminski, P. G., et al. (2013) · Nature Medicine · doi:10.1038/nm.3282 · Cited by 866
Gut-liver axis: Pathophysiological concepts and clinical implications
Tilg, H., Adolph, T. E., & Trauner, M. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.09.017 · Cited by 843
Roles for chemokines in liver disease
Marra, F., & Tacke, F. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.06.043 · Cited by 829
Self-citationVilar-Gomez, E., Calzadilla-Bertot, L., Wai-Sun Wong, V., Castellanos, M., Aller-de la Fuente, R., Metwally, M., Eslam, M., Gonzalez-Fabian, L., Alvarez-Quiñones Sanz, M., Conde-Martin, A. F., et al. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.04.034 · Cited by 806
A Randomized, Controlled Trial of the Pan-PPAR Agonist Lanifibranor in NASH
Francque, S. M., Bedossa, P., Ratziu, V., Anstee, Q. M., Bugianesi, E., Sanyal, A. J., Loomba, R., Harrison, S. A., Balabanska, R., Mateva, L., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2036205 · Cited by 801
Self-citationNonalcoholic fatty liver disease as a nexus of metabolic and hepatic diseases
Samuel, V. T., & Shulman, G. I. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.08.002 · Cited by 745
Wen, Y., Lambrecht, J., Ju, C., & Tacke, F. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-00558-8 · Cited by 695
Self-citationWolf, M. J., Adili, A., Piotrowitz, K., Abdullah, Z., Boege, Y., Stemmer, K., Ringelhan, M., Simonavicius, N., Egger, M., Wohlleber, D., et al. (2014) · Cancer Cell · doi:10.1016/j.ccell.2014.09.003 · Cited by 678
Mortality in biopsy-confirmed nonalcoholic fatty liver disease: results from a nationwide cohort
Simon, T. G., Roelstraete, B., Khalili, H., Hagström, H., & Ludvigsson, J. F. (2021) · Gut · doi:10.1136/gutjnl-2020-322786 · Cited by 673
Mechanisms of Fibrosis Development in Nonalcoholic Steatohepatitis
Schwabe, R. F., Tabas, I., & Pajvani, U. B. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.311 · Cited by 671
Hernández–Gea, V., Ghiassi–Nejad, Z., Rozenfeld, R., Gordon, R., Fiel, M. I., Yue, Z., Czaja, M. J., & Friedman, S. L. (2012) · Gastroenterology · doi:10.1053/j.gastro.2011.12.044 · Cited by 654
Self-citationLassailly, G., Caiazzo, R., Ntandja-Wandji, L.-C., Gnemmi, V., Baud, G., Verkindt, H., Ningarhari, M., Louvet, A., Leteurtre, E., Raverdy, V., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.06.006 · Cited by 622
Remmerie, A., Martens, L., Thoné, T., Castoldi, A., Seurinck, R., Pavie, B., Roels, J., Vanneste, B., De Prijck, S., Vanhockerhout, M., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.08.004 · Cited by 592
Immune cell-mediated features of non-alcoholic steatohepatitis
Huby, T., & Gautier, E. L. (2022) · Nature Reviews Immunology · doi:10.1038/s41577-021-00639-3 · Cited by 573
Buch, S., Stickel, F., Trépo, E., Way, M., Herrmann, A., Nischalke, H. D., Brosch, M., Rosendahl, J., Berg, T., Ridinger, M., et al. (2015) · Nature Genetics · doi:10.1038/ng.3417 · Cited by 565
Peiseler, M., Schwabe, R., Hampe, J., Kubes, P., Heikenwälder, M., & Tacke, F. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.06.012 · Cited by 564
Self-citationAn acute immune response underlies the benefit of cardiac stem cell therapy
Vagnozzi, R. J., Maillet, M., Sargent, M. A., Khalil, H., Johansen, A. K. Z., Schwanekamp, J. A., York, A. J., Huang, V. H., Nahrendorf, M., Sadayappan, S., et al. (2019) · Nature · doi:10.1038/s41586-019-1802-2 · Cited by 557
Krenkel, O., Puengel, T., Govaere, O., Abdallah, A. T., Mossanen, J. C., Kohlhepp, M., Liepelt, A., Lefebvre, E., Luedde, T., Hellerbrand, C., et al. (2018) · Hepatology · doi:10.1002/hep.29544 · Cited by 557
Self-citationAuto-aggressive CXCR6+ CD8 T cells cause liver immune pathology in NASH
Dudek, M., Pfister, D., Donakonda, S., Filpe, P., Schneider, A., Laschinger, M., Hartmann, D., Hüser, N., Meiser, P., Bayerl, F., et al. (2021) · Nature · doi:10.1038/s41586-021-03233-8 · Cited by 518
Self-citationHarrison, S. A., Wong, V. W.-S., Okanoue, T., Bzowej, N., Vuppalanchi, R., Younes, Z., Kohli, A., Sarin, S., Caldwell, S. H., Alkhouri, N., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.02.027 · Cited by 497
Role of bile acids and their receptors in gastrointestinal and hepatic pathophysiology
Fuchs, C. D., & Trauner, M. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-021-00566-7 · Cited by 490
Seidman, J. S., Troutman, T. D., Sakai, M., Gola, A., Spann, N. J., Bennett, H., Bruni, C. M., Ouyang, Z., Li, R. Z., Sun, X., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.04.001 · Cited by 443
Pluripotent stem cell-derived CAR-macrophage cells with antigen-dependent anti-cancer cell functions
Zhang, L., Tian, L., Dai, X., Yu, H., Wang, J., Lei, A., Zhu, M., Xu, J., Zhao, W., Zhu, Y., et al. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-00983-2 · Cited by 425
Single-cell transcriptomics uncovers zonation of function in the mesenchyme during liver fibrosis
Dobie, R., Wilson-Kanamori, J. R., Henderson, B. E. P., Smith, J. R., Matchett, K. P., Portman, J. R., Wallenborg, K., Picelli, S., Zagorska, A., Pendem, S. V., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.024 · Cited by 420
Tran, S., Baba, I., Poupel, L., Dussaud, S., Moreau, M., Gélineau, A., Marcelin, G., Magréau-Davy, E., Ouhachi, M., Lesnik, P., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.06.003 · Cited by 400
Malehmir, M., Pfister, D., Gallage, S., Szydlowska, M., Inverso, D., Kotsiliti, E., Leone, V., Peiseler, M., Surewaard, B. G. J., Rath, D., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0379-5 · Cited by 398
Self-citationUpdate on NAFLD genetics: From new variants to the clinic
Trépo, E., & Valenti, L. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.02.020 · Cited by 393
A role for autophagy during hepatic stellate cell activation
Thoen, L. F. R., Guimarães, E. L. M., Dollé, L., Mannaerts, I., Najimi, M., Sokal, E., & van Grunsven, L. A. (2011) · Journal of Hepatology · doi:10.1016/j.jhep.2011.07.010 · Cited by 385
Harrison, S. A., Abdelmalek, M. F., Caldwell, S., Shiffman, M. L., Diehl, A. M., Ghalib, R., Lawitz, E. J., Rockey, D. C., Schall, R. A., Jia, C., et al. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.07.006 · Cited by 384
Daemen, S., Gainullina, A., Kalugotla, G., He, L., Chan, M. M., Beals, J. W., Liss, K. H., Klein, S., Feldstein, A. E., Finck, B. N., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2020.108626 · Cited by 378
Ratziu, V., Sanyal, A., Harrison, S. A., Wong, V. W., Francque, S., Goodman, Z., Aithal, G. P., Kowdley, K. V., Seyedkazemi, S., Fischer, L., et al. (2020) · Hepatology · doi:10.1002/hep.31108 · Cited by 378
Self-citationAdaptive immunity: an emerging player in the progression of NAFLD
Sutti, S., & Albano, E. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0210-2 · Cited by 374
Azzu, V., Vacca, M., Virtue, S., Allison, M., & Vidal-Puig, A. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.12.054 · Cited by 369
Chalasani, N., Abdelmalek, M. F., Garcia-Tsao, G., Vuppalanchi, R., Alkhouri, N., Rinella, M., Noureddin, M., Pyko, M., Shiffman, M., Sanyal, A., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.296 · Cited by 358
Self-citationThymic development of unconventional T cells: how NKT cells, MAIT cells and γδ T cells emerge
Pellicci, D. G., Koay, H., & Berzins, S. P. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-020-0345-y · Cited by 346
Thomas, J. A., Pope, C., Wojtacha, D., Robson, A. J., Gordon-Walker, T. T., Hartland, S., Ramachandran, P., Van Deemter, M., Hume, D. A., Iredale, J. P., et al. (2011) · Hepatology · doi:10.1002/hep.24315 · Cited by 346
Nonalcoholic steatohepatitis: the role of peroxisome proliferator-activated receptors
Francque, S., Szabo, G., Abdelmalek, M. F., Byrne, C. D., Cusi, K., Dufour, J.-F., Roden, M., Sacks, F., & Tacke, F. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00366-5 · Cited by 316
Self-citationLefere, S., Puengel, T., Hundertmark, J., Penners, C., Frank, A. K., Guillot, A., de Muynck, K., Heymann, F., Adarbes, V., Defrêne, E., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.04.025 · Cited by 310
Self-citationMucosal-associated invariant T cells and disease
Toubal, A., Nel, I., Lotersztajn, S., & Lehuen, A. (2019) · Nature Reviews Immunology · doi:10.1038/s41577-019-0191-y · Cited by 300
Adipose-resident group 1 innate lymphoid cells promote obesity-associated insulin resistance
O’Sullivan, T. E., Rapp, M., Fan, X., Weizman, O.-E., Bhardwaj, P., Adams, N. M., Walzer, T., Dannenberg, A. J., & Sun, J. C. (2016) · Immunity · doi:10.1016/j.immuni.2016.06.016 · Cited by 293
Hepatic stellate cell autophagy inhibits extracellular vesicle release to attenuate liver fibrosis
Gao, J., Wei, B., de Assuncao, T. M., Liu, Z., Hu, X., Ibrahim, S., Cooper, S. A., Cao, S., Shah, V. H., & Kostallari, E. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.04.044 · Cited by 288
Ma, P.-F., Gao, C.-C., Yi, J., Zhao, J.-L., Liang, S.-Q., Zhao, Y., Ye, Y.-C., Bai, J., Zheng, Q.-J., Dou, K.-F., et al. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.05.022 · Cited by 284
Cellular and Molecular Mechanisms Underlying Liver Fibrosis Regression
Caligiuri, A., Gentilini, A., Pastore, M., Gitto, S., & Marra, F. (2021) · Cells · doi:10.3390/cells10102759 · Cited by 283
Boland, M. L., Laker, R. C., Mather, K., Nawrocki, A., Oldham, S., Boland, B. B., Lewis, H., Conway, J., Naylor, J., Guionaud, S., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-0209-6 · Cited by 270
Baeck, C., Wei, X., Bartneck, M., Fech, V., Heymann, F., Gassler, N., Hittatiya, K., Eulberg, D., Luedde, T., Trautwein, C., et al. (2014) · Hepatology · doi:10.1002/hep.26783 · Cited by 270
Self-citationNeutrophils contribute to spontaneous resolution of liver inflammation and fibrosis via microRNA-223
Calvente, C. J., Tameda, M., Johnson, C. D., del Pilar, H., Lin, Y. C., Adronikou, N., De Mollerat Du Jeu, X., Llorente, C., Boyer, J., & Feldstein, A. E. (2019) · Journal of Clinical Investigation · doi:10.1172/jci122258 · Cited by 268
The PNPLA3 I148M variant modulates the fibrogenic phenotype of human hepatic stellate cells
Bruschi, F. V., Claudel, T., Tardelli, M., Caligiuri, A., Stulnig, T. M., Marra, F., & Trauner, M. (2017) · Hepatology · doi:10.1002/hep.29041 · Cited by 268
Wehr, A., Baeck, C., Heymann, F., Niemietz, P. M., Hammerich, L., Martin, C., Zimmermann, H. W., Pack, O., Gassler, N., Hittatiya, K., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202909 · Cited by 268
Self-citationNKT-Associated Hedgehog and Osteopontin Drive Fibrogenesis in Non-Alcoholic Fatty Liver Disease
Syn, W.-K., Agboola, K. M., Swiderska, M., Michelotti, G. A., Liaskou, E., Pang, H., Xie, G., Philips, G., Chan, I. S., Karaca, G. F., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-301857 · Cited by 266
Bataller, R., Arab, J. P., & Shah, V. H. (2022) · New England Journal of Medicine · doi:10.1056/nejmra2207599 · Cited by 259
Single-cell technologies in hepatology: new insights into liver biology and disease pathogenesis
Ramachandran, P., Matchett, K. P., Dobie, R., Wilson-Kanamori, J. R., & Henderson, N. C. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0304-x · Cited by 253
Krenkel, O., Hundertmark, J., Ritz, T., Weiskirchen, R., & Tacke, F. (2019) · Cells · doi:10.3390/cells8050503 · Cited by 241
Self-citationA subset of Kupffer cells regulates metabolism through the expression of CD36
Blériot, C., Barreby, E., Dunsmore, G., Ballaire, R., Chakarov, S., Ficht, X., De Simone, G., Andreata, F., Fumagalli, V., Guo, W., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.08.006 · Cited by 236
Mucosal-associated invariant T cells are a profibrogenic immune cell population in the liver
Hegde, P., Weiss, E., Paradis, V., Wan, J., Mabire, M., Sukriti, S., Rautou, P.-E., Albuquerque, M., Picq, O., Gupta, A. C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04450-y · Cited by 232
Alkhouri, N., Herring, R., Kabler, H., Kayali, Z., Hassanein, T., Kohli, A., Huss, R. S., Zhu, Y., Billin, A. N., Damgaard, L. H., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.04.003 · Cited by 230
Self-citationBates, J., Vijayakumar, A., Ghoshal, S., Marchand, B., Yi, S., Kornyeyev, D., Zagorska, A., Hollenback, D., Walker, K., Liu, K., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.04.037 · Cited by 230
Neutrophils as potential therapeutic targets in hepatocellular carcinoma
Geh, D., Leslie, J., Rumney, R., Reeves, H. L., Bird, T. G., & Mann, D. A. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-021-00568-5 · Cited by 223
Ratziu, V., de Guevara, L., Safadi, R., Poordad, F., Fuster, F., Flores-Figueroa, J., Arrese, M., Fracanzani, A. L., Ben Bashat, D., Lackner, K., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01495-3 · Cited by 222
Self-citationKrenkel, O., Hundertmark, J., Abdallah, A. T., Kohlhepp, M., Puengel, T., Roth, T., Branco, D. P. P., Mossanen, J. C., Luedde, T., Trautwein, C., et al. (2020) · Gut · doi:10.1136/gutjnl-2019-318382 · Cited by 220
Self-citationKoda, Y., Teratani, T., Chu, P.-S., Hagihara, Y., Mikami, Y., Harada, Y., Tsujikawa, H., Miyamoto, K., Suzuki, T., Taniki, N., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24734-0 · Cited by 219
Calle, R. A., Amin, N. B., Carvajal-Gonzalez, S., Ross, T. T., Bergman, A., Aggarwal, S., Crowley, C., Rinaldi, A., Mancuso, J., Aggarwal, N., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01489-1 · Cited by 219
Microbiome-derived ethanol in nonalcoholic fatty liver disease
Meijnikman, A. S., Davids, M., Herrema, H., Aydin, O., Tremaroli, V., Rios-Morales, M., Levels, H., Bruin, S., de Brauw, M., Verheij, J., et al. (2022) · Nature Medicine · doi:10.1038/s41591-022-02016-6 · Cited by 215
Report on the AASLD/EASL joint workshop on clinical trial endpoints in NAFLD
Rinella, M. E., Tacke, F., Sanyal, A. J., & Anstee, Q. M. (2019) · Journal of Hepatology · doi:10.1016/j.jhep.2019.04.019 · Cited by 209
Self-citationMechanisms of liver fibrosis resolution
Tacke, F., & Trautwein, C. (2015) · Journal of Hepatology · doi:10.1016/j.jhep.2015.03.039 · Cited by 207
Self-citationSafety profile of autologous macrophage therapy for liver cirrhosis
Moroni, F., Dwyer, B. J., Graham, C., Pass, C., Bailey, L., Ritchie, L., Mitchell, D., Glover, A., Laurie, A., Doig, S., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0599-8 · Cited by 202
XCR1+ type 1 conventional dendritic cells drive liver pathology in non-alcoholic steatohepatitis
Deczkowska, A., David, E., Ramadori, P., Pfister, D., Safran, M., Li, B., Giladi, A., Jaitin, D. A., Barboy, O., Cohen, M., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01344-3 · Cited by 197
Loomba, R. S., Wong, R. J., Fraysse, J., Shreay, S., Li, S., Harrison, S. A., & Gordon, S. C. (2020) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15679 · Cited by 187
Self-citationBöttcher, K., Rombouts, K., Saffioti, F., Roccarina, D., Rosselli, M., Hall, A., Luong, T., Tsochatzis, E. A., Thorburn, D., & Pinzani, M. (2018) · Hepatology · doi:10.1002/hep.29782 · Cited by 183
Wang, S., Li, K., Pickholz, E., Dobie, R., Matchett, K. P., Henderson, N. C., Carrico, C., Driver, I., Borch Jensen, M., Chen, L., et al. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.add3949 · Cited by 176
Self-citationNKp46-Mediated Killing of Human and Mouse Hepatic Stellate Cells Attenuates Liver Fibrosis
Gur, C., Doron, S., Kfir-Erenfeld, S., Horwitz, E., Abu-tair, L., Safadi, R., & Mandelboim, O. (2012) · Gut · doi:10.1136/gutjnl-2011-301400 · Cited by 173
Sanyal, A. J., Anstee, Q. M., Trauner, M., Lawitz, E. J., Abdelmalek, M. F., Ding, D., Han, L., Jia, C., Huss, R. S., Chung, C., et al. (2022) · Hepatology · doi:10.1002/hep.32204 · Cited by 171
Luukkonen, P. K., Qadri, S., Ahlholm, N., Porthan, K., Männistö, V., Sammalkorpi, H., Penttilä, A. K., Hakkarainen, A., Lehtimäki, T. E., Gaggini, M., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2021.10.013 · Cited by 170
Carlsson, B., Lindén, D., Brolén, G., Liljeblad, M., Bjursell, M., Romeo, S., & Loomba, R. (2020) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15738 · Cited by 169
Self-citationMoles, A., Murphy, L., Wilson, C. L., Chakraborty, J. B., Fox, C., Park, E. J., Mann, J., Oakley, F., Howarth, R., Brain, J., et al. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2013.12.005 · Cited by 169
Lai, K. K. Y., Kweon, S.-M., Chi, F., Hwang, E., Kabe, Y., Higashiyama, R., Qin, L., Yan, R., Wu, R. P., Lai, K., et al. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.01.021 · Cited by 165
Haas, J. T., Vonghia, L., Mogilenko, D. A., Verrijken, A., Molendi-Coste, O., Fleury, S., Deprince, A., Nikitin, A., Woitrain, E., Ducrocq-Geoffroy, L., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0076-1 · Cited by 155
SUMOylation inhibitors synergize with FXR agonists in combating liver fibrosis
Zhou, J., Cui, S., He, Q., Guo, Y., Pan, X., Zhang, P., Huang, N., Ge, C., Wang, G., Gonzalez, F. J., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14138-6 · Cited by 154
Heterogeneity of HSCs in a Mouse Model of NASH
Rosenthal, S. B., Liu, X., Ganguly, S., Dhar, D., Pasillas, M. P., Ricciardelli, E., Li, R. Z., Troutman, T. D., Kisseleva, T., Glass, C. K., et al. (2021) · Hepatology · doi:10.1002/hep.31743 · Cited by 145
Psaraki, A., Ntari, L., Karakostas, C., Korrou‐Karava, D., & Roubelakis, M. G. (2022) · Hepatology · doi:10.1002/hep.32129 · Cited by 145
Cell therapy for advanced liver diseases: repair or rebuild
Dwyer, B. J., Macmillan, M. T., Brennan, P. N., & Forbes, S. J. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2020.09.014 · Cited by 141
Breakthroughs in therapies for NASH and remaining challenges
Ratziu, V., Francque, S., & Sanyal, A. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.04.002 · Cited by 132
Loomba, R., Ratziu, V., Harrison, S. A., Loomba, R., McFarlane, S. C., Tamaki, N., Ratziu, V., Abdelmalek, M. F., Rinella, M. E., Anstee, Q. M., et al. (2022) · Gastroenterology · doi:10.1053/j.gastro.2021.10.051 · Cited by 127
Self-citationThe Emerging Role of B Cells in the Pathogenesis of NAFLD
Barrow, F., Khan, S., Wang, H., & Revelo, X. S. (2021) · Hepatology · doi:10.1002/hep.31889 · Cited by 126
Loss of hepatic Mboat7 leads to liver fibrosis
Thangapandi, V. R., Knittelfelder, O., Brosch, M., Patsenker, E., Vvedenskaya, O., Buch, S., Hinz, S., Hendricks, A., Nati, M., Herrmann, A., et al. (2021) · Gut · doi:10.1136/gutjnl-2020-320853 · Cited by 125
Role of bile acids in inflammatory liver diseases
Evangelakos, I., Heeren, J., Verkade, E., & Kuipers, F. (2021) · Seminars in Immunopathology · doi:10.1007/s00281-021-00869-6 · Cited by 121
Promises of microbiome-based therapies
Bajaj, J. S., Ng, S. C., & Schnabl, B. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2021.12.003 · Cited by 119
Understanding the cellular interactome of non-alcoholic fatty liver disease
Wallace, S. J., Tacke, F., Schwabe, R. F., & Henderson, N. C. (2022) · JHEP Reports · doi:10.1016/j.jhepr.2022.100524 · Cited by 116
Self-citationGuillot, A., Winkler, M., Silva Afonso, M., Aggarwal, A., Lopez, D., Berger, H., Kohlhepp, M. S., Liu, H., Özdirik, B., Eschrich, J., et al. (2023) · Hepatology · doi:10.1097/hep.0000000000000270 · Cited by 116
Self-citationNaoumov, N. V., Brees, D., Loeffler, J., Chng, E., Ren, Y., Lopez, P., Tai, D., Lamle, S., & Sanyal, A. J. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.06.018 · Cited by 115
Nachit, M., Kwanten, W. J., Thissen, J.-P., Op De Beeck, B., Van Gaal, L., Vonghia, L., Verrijken, A., Driessen, A., Horsmans, Y., Francque, S., et al. (2021) · Journal of Hepatology · doi:10.1016/j.jhep.2021.02.037 · Cited by 114
Maladaptive regeneration - the reawakening of developmental pathways in NASH and fibrosis
Zhu, C., Tabas, I., Schwabe, R. F., & Pajvani, U. B. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00365-6 · Cited by 112
Lawitz, E. J., Shevell, D. E., Tirucherai, G. S., Du, S., Chen, W., Kavita, U., Coste, A., Poordad, F., Karsdal, M., Nielsen, M., et al. (2022) · Hepatology · doi:10.1002/hep.32181 · Cited by 107
The liver matrisome – looking beyond collagens
Arteel, G. E., & Naba, A. (2020) · JHEP Reports · doi:10.1016/j.jhepr.2020.100115 · Cited by 107
O’Farrell, M., Duke, G. M., Crowley, R., BUCKLEY, D. I., Martins, E. B., Bhattacharya, D., Friedman, S. L., & Kemble, G. W. (2022) · Scientific Reports · doi:10.1038/s41598-022-19459-z · Cited by 104
Self-citationSubramanian, S., Busch, C. J.-L., Molawi, K., Geirsdottir, L., Maurizio, J., Vargas Aguilar, S., Belahbib, H., Gimenez, G., Yuda, R. A. A., Burkon, M., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01146-w · Cited by 103
Two Faces of Neutrophils in Liver Disease Development and Progression
Cho, Y., & Szabó, G. (2020) · Hepatology · doi:10.1002/hep.31680 · Cited by 103
The NLRP3 inflammasome in alcoholic and nonalcoholic steatohepatitis
Knorr, J., Wree, A., Tacke, F., & Feldstein, A. E. (2020) · Seminars in Liver Disease · doi:10.1055/s-0040-1708540 · Cited by 99
Self-citationPharmacological intervention in hepatic stellate cell activation and hepatic fibrosis
Schon, H.-T., Bartneck, M., Borkham-Kamphorst, E., Nattermann, J., Lammers, T., Tacke, F., & Weiskirchen, R. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00033 · Cited by 97
Self-citationNuclear receptors linking metabolism, inflammation, and fibrosis in nonalcoholic fatty liver disease
Puengel, T., Liu, H., Guillot, A., Heymann, F., Tacke, F., & Peiseler, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052668 · Cited by 95
Self-citationAcetyl-CoA Carboxylase Inhibition Improves Multiple Dimensions of NASH Pathogenesis in Model Systems
Ross, T. T., Crowley, C., Kelly, K. L., Rinaldi, A., Beebe, D. A., Lech, M. P., Martinez, R. V., Carvajal-Gonzalez, S., Boucher, M., Hirenallur-Shanthappa, D., et al. (2020) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2020.06.001 · Cited by 94
Majzoub, A. M., Nayfeh, T., Barnard, A., Munaganuru, N., Dave, S., Singh, S., Murad, M. H., & Loomba, R. (2021) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.16583 · Cited by 92
Self-citationThe Commensal Microbe V eillonella as a Marker for Response to an FGF19 Analog in NASH
Loomba, R., Ling, L., Dinh, D. M., DePaoli, A. M., Lieu, H. D., Harrison, S. A., & Sanyal, A. J. (2021) · Hepatology · doi:10.1002/hep.31523 · Cited by 88
Self-citationPuengel, T., Vos, S. D., Hundertmark, J., Kohlhepp, M. S., Güldiken, N., Pujuguet, P., Auberval, M., Marsais, F., Shoji, K. F., Sanière, L., et al. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9041140 · Cited by 86
Self-citationPNPLA3 as a therapeutic target for fatty liver disease: the evidence to date
Cherubini, A., Casirati, E., Tomasi, M., & Valenti, L. (2021) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2021.2018418 · Cited by 79
Bhattacharya, D., Basta, B. N., Mato, J. M., Craig, A. J., Fernández‐Ramos, D., Lopitz‐Otsoa, F., Tsvirkun, D., Hayardeny, L., Chandar, V., Schwartz, R. E., et al. (2021) · JHEP Reports · doi:10.1016/j.jhepr.2021.100237 · Cited by 79
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Metadata
- Authors
- Tacke, F., Puengel, T., Loomba, R., & Friedman, S. L.
- Affiliations
- Stiftung Charité (DE)
- Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE)
- University of California San Diego (US)
- Icahn School of Medicine at Mount Sinai (US)
- Corresponding author
- Tacke, Frank
- Venue
- Journal of Hepatology
- Publisher
- Elsevier BV
- Published
- 2023-08
- Volume
- 79
- Issue
- 2
- Pages
- 552-566
- ISSN
- 0168-8278 (ISSN-L)
- PMC
- PMC12164378
- OpenAlex
- W4365517553
- Cited by
- 321
- References
- 162
- Citations by year
- 2026: 84 · 2025: 112 · 2024: 93 · 2023: 31
- FWCI
- 12.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Hepatology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (P01HL147835)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK120515, R01DK106419, R01DK121378, R01DK124318, U01DK061734, U01DK130190)
- National Center for Advancing Translational Sciences (5UL1TR001442)
- Deutsche Forschungsgemeinschaft
- National Institutes of Health (3UL1TR004419, 5P30CA196521, R01 DK 121154-01A1, R01 DK128289)
- Bundesministerium für Bildung und Forschung
- National Institute on Alcohol Abuse and Alcoholism (U01AA029019)
- Topics
- Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Keywords
- nonalcoholic steatohepatitis, non-alcoholic fatty liver disease, liver fibrosis, anti-inflammatory therapy, antifibrotic therapy, nuclear receptor agonists, obeticholic acid, lanifibranor, resmetirom, semaglutide, tirzepatide, gut microbiota, adipose tissue inflammation, hepatocyte death, innate lymphoid cells, macrophages, galectin-3 inhibitors, chemokine receptor inhibitors, hepatic stellate cells, myofibroblasts, cell therapy, chimeric antigen receptor T cells, disease heterogeneity
- MeSH terms
- Anti-Inflammatory Agents, Humans, Liver, Liver Cirrhosis, Receptors, Cytoplasmic and Nuclear, Hepatocytes, Non-alcoholic Fatty Liver Disease
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-05, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
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Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
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