The DOI matches its Crossref record; 96 of the 100 references it cites were found in a registry or an index; 2 of the 88 sources its claims cite were checked for support.
Iron homeostasis in host defence and inflammation
Open accessAbstract
Iron is an essential trace element for multicellular organisms and nearly all microorganisms. Although iron is abundant in the environment, common forms of iron are minimally soluble and therefore poorly accessible to biological organisms. Microorganisms entering a mammalian host face multiple mechanisms that further restrict their ability to obtain iron and thereby limit their pathogenicity. Iron levels also modulate host defence, as iron content in macrophages regulates their cytokine production. Here, we review recent advances that highlight the role of systemic and cellular iron-regulating mechanisms in protecting hosts from infection, emphasizing aspects that are applicable to human health and disease.
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58 Not checked yet · 13 Own interpretation · 10 No basis given · 1 Supported · 1 Partly supported · accuracy not yet measured
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In the paper
“By contrast, macrophage expression of TFR1, which mediates iron delivery to endosomes, is decreased by IFNγ exposure during intracellular infections73.”
§ Iron homeostasis in host defence and inflammation > Hepcidin-independent iron sequestration > Iron-sequestering proteins
What the sources say
- Partly supportedcites [73] Byrd, T. F. & Horwitz, M. A. Interferon gamma-activated human monocytes downregulate transferrin receptors and inhibit the intracellular multiplication of Legionella pneumophila by limiting the availability of iron. J. Clin. Invest. 83, 1457–1465 (1989). sourceExperimental — accuracy not yet measured
The Results report that IFNγ-activated human monocytes had decreased transferrin-receptor expression, and the Discussion reports 73% fewer transferrin-binding sites. The receptor measurements were made in cultured monocytes; the paper does not establish the decrease in infected macrophages or across intracellular infections generally. Page numbers are unavailable in our copy. (LLM, conf=0.84)
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In the paper
“These agents were effective against fulminant V. vulnificus infection in hepcidin-deficient mice52.”
§ Iron homeostasis in host defence and inflammation > Therapeutic opportunities and challenges
What the sources say
- Supportedcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. source
The Results section reports that minihepcidin PR73 markedly improved survival in hepcidin-deficient (Hamp1−/−) mice infected with V. vulnificus. It also reports increased survival when PR73 was given three hours after infection. Page numbers were not supplied. (LLM, conf=0.94)
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In the paper
“Therefore, we propose that hepcidin-induced hypoferraemia functions to limit the availability of non-transferrin-bound iron during infections.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
hedgeddirect- Asserted: passes — The authors put it forward as true.
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In the paper
“We propose that the hypoferraemic response evolved to provide an increased capacity for transferrin to bind iron that would be released during acute infection and during the associated destruction of tissues and erythrocytes, and so limit the generation of non-transferrin-bound iron that can be readily used by many microorganisms.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Hepcidin-induced hypoferraemia and host defence
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- Rests on an assumption: Most microorganisms depend absolutely on exogenous iron for survival.
- Rests on an assumption: Malarial parasites require iron at both the liver and erythrocyte stages.
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
“This mechanism is particularly effective against bacterial strains that lack siderophore-mediated iron uptake (for example, marine Vibrio species).”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
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In the paper
“Interestingly, mice infected with siderophilic bacteria were rescued by treatment with potent hepcidin agonists (known as minihepcidins) that induced hypoferraemia. These treatments had little or no effect on iron stores but redistributed iron from the extracellular space into macrophages.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“This led to the concept of iron-targeted nutritional immunity as a set of constitutive and inducible mechanisms that deny iron to invading pathogens and thereby limit their ability to harm the host1.”
§ Iron homeostasis in host defence and inflammation > Abstract
What the sources say
- Not checked yetcites [1] Weinberg, E. D. Nutritional immunity: host's attempt to withhold iron from microbial invaders. JAMA 231, 39–41 (1975). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Hepcidin-deficient mice die of sepsis in less than 16 hours after subcutaneous infection with V. vulnificus at doses that are otherwise well tolerated by wild-type mice52.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Hepcidin-deficient mice are also much more susceptible than wild-type mice to death from infection with Y. enterocolitica (D. Stefanova, Y. Bulut, T.G. and E.N., unpublished observations) and certain attenuated strains of Y. pestis47.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [47] Quenee, L. E. et al. Hereditary hemochromatosis restores the virulence of plague vaccine strains. J. Infect. Dis. 206, 1050–1058 (2012). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Ex vivo growth of V. vulnificus in mouse sera was greatly accelerated by the addition of ferric iron in amounts that exceeded the binding capacity of transferrin52.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. source
plaindirect- Asserted: passes — The authors put it forward as true.
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- It may state two separate claims as one. 36
- Probably not a substantial claim. 6
- The quote only partly states this claim. 1
In the paper
“Susceptibility to death from infection with V. vulnificus correlated with the presence of non-transferrin-bound iron in the mouse sera and with the ability of sera from these mice to support rapid in vitro growth of V. vulnificus.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. source
plaincorrelational- 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
“Infection and inflammation induce hepcidin production, driving a decrease in plasma iron concentrations by inhibiting the absorption of iron and promoting the sequestration of iron in macrophages.”
§ Iron homeostasis in host defence and inflammation > Abstract
What the sources say
- Not checked yetcites [26] Nicolas, G. et al. The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation. J. Clin. Invest. 110, 1037–1044 (2002). source
- Not checked yetcites [27] Goodnough, L. T., Nemeth, E. & Ganz, T. Detection, evaluation, and management of iron-restricted erythropoiesis. Blood 116, 4754–4761 (2010). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Lactic acid bacteria (also known as Lactobacillales) are normal components of the intestinal flora and have little or no requirement for iron; they thrive in the relatively iron-poor environment of the human intestine, but they may be displaced by other microorganisms when iron is administered60.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Intestinal flora
What the sources say
- Not checked yetcites [60] Bailey, J. R., Probert, C. S. & Cogan, T. A. Identification and characterisation of an iron-responsive candidate probiotic. PLoS ONE 6, e26507 (2011). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“However, the local and systemic responses to aseptic inflammation in vivo are preserved in the absence of either of the two IREBPs3, which suggests that the role of the IREBPs in host defence and inflammation is minor or that the two IREBPs have mostly overlapping functions, an issue that needs to be examined further.”
§ Iron homeostasis in host defence and inflammation > Abstract
What the sources say
- Not checked yetcites [3] Viatte, L., Grone, H. J., Hentze, M. W. & Galy, B. In vivo role(s) of the iron regulatory proteins (IRP) 1 and 2 in aseptic local inflammation. J. Mol. Med. 87, 913–921 (2009). source
hedged- Asserted: passes — The authors put it forward as true.
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Probably not a substantial claim. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Moreover, non-transferrin-bound iron can amplify tissue injury either because it catalyses the extracellular production of injurious reactive oxygen species (ROS) or because it is rapidly taken up some cell types, causing cellular iron overload with the secondary generation of ROS.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Hepcidin-induced hypoferraemia and host defence
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
- Rests on an assumption: Malarial parasites require iron at both the liver and erythrocyte stages.
In the paper
“This mechanism may function to prevent superinfection by additional malaria parasites during subsequent exposures to malaria-bearing mosquitoes, and it provides a form of innate immune protection in infants and children who have not yet developed an adaptive immune response to malarial parasites31.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Hepcidin-induced redistribution of iron is protective in malaria
What the sources say
- Not checked yetcites [31] Portugal, S. et al. Host-mediated regulation of superinfection in malaria. Nat. Med. 17, 732–737 (2011). In pre-immune children, malaria parasitaemia induces hepcidin expression and redistributes iron from hepatocytes to macrophages, thereby interfering with the hepatic stage of superinfection by another malarial strain. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Tissue iron overload and resulting toxicity is proportional to the severity and duration of hepcidin deficiency, and results in progressive iron-mediated damage to the liver, endocrine glands and cardiac myocytes.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Hereditary haemochromatosis
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Interestingly, although most bacterial and some viral infections (such as influenza virus and HIV) rapidly increase hepcidin production in humans and mouse models, hepatitis B and hepatitis C virus infections fail to elicit systemic inflammatory responses and hepcidin production30.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Stimulation of hepcidin synthesis during infection
What the sources say
- Not checked yetcites [30] Armitage, A. E. et al. Distinct patterns of hepcidin and iron regulation during HIV-1, HBV, and HCV infections. Proc. Natl Acad. Sci. USA 111, 12187–12192 (2014). This study shows that not all infections induce hepcidin: no induction of hepcidin or hypoferraemia was observed during the viraemic phase of hepatitis B or hepatitis C virus infection. source
plaindirect- Asserted: passes — The authors put it forward as true.
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The role of hepcidin as the iron-regulatory hormone that acts on ferroportin to modulate iron absorption and systemic iron distribution is now well accepted, but the strong connection between hepcidin and host defence is less well appreciated.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Stimulation of hepcidin synthesis during infection
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Probably not a substantial claim.
In the paper
“Iron depletion of macrophages could therefore mimic the effects of hypoxia, stabilizing HIF1α and promoting the transcription and synthesis of IL-1β68 and perhaps other cytokines.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Iron deficiency and inflammation
What the sources say
- Not checked yetcites [68] Peyssonnaux, C. et al. Cutting edge: essential role of hypoxia inducible factor-1α in development of lipopolysaccharide-induced sepsis. J. Immunol. 178, 7516–7519 (2007). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Malaria infection causes inflammation and increases hepcidin levels, redistributing iron to macrophages and, in the long term, away from hepatocytes that normally support the initial stage of infection.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Hepcidin-induced redistribution of iron is protective in malaria
plaindirect- Asserted: passes — The authors put it forward as true.
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Also similar to defensins, hepcidin has direct antimicrobial activity in vitro, but the concentrations and conditions required for this activity seem to be outside of the physiological range.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Stimulation of hepcidin synthesis during infection
hedged- 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.
In the paper
“In ex vivo erythrocytes from iron-deficient donors, the malarial parasite Plasmodium falciparum invades fewer cells and shows slower intracellular growth than in erythrocytes from iron-replete donors66.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Protective effects of iron deficiency in malaria
What the sources say
- Not checked yetcites [66] Clark, M. A. et al. Host iron status and iron supplementation mediate susceptibility to erythrocytic stage Plasmodium falciparum. Nat. Commun. 5, 4446 (2014). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“IL-1β mediates systemic inflammation and activates important host defence mechanisms69.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Iron deficiency and inflammation
What the sources say
- Not checked yetcites [69] Horino, T. et al. Interleukin-1-deficient mice exhibit high sensitivity to gut-derived sepsis caused by Pseudomonas aeruginosa. Cytokine 30, 339–346 (2005). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Indeed, a recent study showed that exogenous hepcidin is protective against renal ischaemia–reperfusion injury and oxidative stress, and that hepcidin deficiency exacerbates these forms of injury32.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Hepcidin-induced hypoferraemia and host defence
What the sources say
- Not checked yetcites [32] Scindia, Y. et al. Hepcidin mitigates renal ischemia–reperfusion injury by modulating systemic iron homeostasis. J. Am. Soc. Nephrol. http://dx.doi.org/10.1681/ASN.2014101037 (2015). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Motivated to understand the connection between iron supplementation and diarrhoeal illness in African children, some but not all studies found an altered composition of the intestinal flora and increased inflammation in children who were treated to prevent or reverse iron deficiency61–63.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Intestinal flora
What the sources say
- Not checked yetcites [61] Zimmermann, M. B. et al. The effects of iron fortification on the gut microbiota in African children: a randomized controlled trial in Cote d'Ivoire. Am. J. Clin. Nutr. 92, 1406–1415 (2010). source
- Not checked yetcites [62] Jaeggi, T. et al. Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants. Gut 64, 731–742 (2015). source
- Not checked yetcites [63] Dostal, A. et al. Effects of iron supplementation on dominant bacterial groups in the gut, faecal SCFA and gut inflammation: a randomised, placebo-controlled intervention trial in South African children. Br. J. Nutr. 112, 547–556 (2014). source
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“Another set of regulatory factors conveys the iron requirements for erythropoiesis and includes the recently identified hormone erythroferrone12, which is produced by erythroblasts in response to erythropoietic stimulation by endogenous or synthetic erythropoietin. Erythroferrone suppresses hepcidin synthesis, making more iron available for enhanced erythropoiesis.”
§ Iron homeostasis in host defence and inflammation > Systemic iron homeostasis > Regulation of hepcidin
What the sources say
- Not checked yetcites [12] Kautz, L. et al. Identification of erythroferrone as an erythroid regulator of iron metabolism. Nat. Genet. 46, 678–684 (2014). source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Although the induction of IL-1β is not primarily modulated by hepcidin, hepcidin causes iron sequestration in macrophages (FIG. 3) and would be expected to have an anti-inflammatory effect67.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Iron deficiency and inflammation
What the sources say
- Not checked yetcites [67] Pagani, A. et al. Low hepcidin accounts for the proinflammatory status associated with iron deficiency. Blood 118, 736–746 (2011). source
hedgeddirect- Asserted: passes — The authors put it forward as true.
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The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Cellular iron overload increases the production of ROS, causing cellular injury.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Hereditary haemochromatosis
plaindirect- Asserted: passes — The authors put it forward as true.
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It may state two separate claims as one.
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In the paper
“Paradoxically, studies in mouse models have shown that infections with intracellular microorganisms that reside in macrophages may be enhanced by hepcidin-induced iron sequestration, and conversely, hepcidin deficiency in mouse models of hereditary haemochromatosis may inhibit the growth of macrophage-resident bacteria, including Mycobacteria tuberculosis53 or Salmonella enterica serovar enterica”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Effects of hepcidin expression and hypoferraemia in infection
What the sources say
- Not checked yetcites [53] Olakanmi, O., Schlesinger, L. S. & Britigan, B. E. Hereditary hemochromatosis results in decreased iron acquisition and growth by Mycobacterium tuberculosis within human macrophages. J. Leukoc. Biol. 81, 195–204 (2007). source
- Not checked yetcites [54] Nairz, M. et al. Absence of functional Hfe protects mice from invasive Salmonella enterica serovar Typhimurium infection via induction of lipocalin-2. Blood 114, 3642–3651 (2009). References 53 and 54 raise the possibility that hepcidin deficiency, while promoting certain extracellular infections, may be protective against intracellular pathogens. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Mice engineered to lack hepcidin fail to develop hypoferraemia after inflammatory stimulation, their serum iron concentrations may even increase during infection or inflammation, and their anaemia of inflammation is milder28,29.”
§ Iron homeostasis in host defence and inflammation > Hepcidin and host defence > Stimulation of hepcidin synthesis during infection
What the sources say
- Not checked yetcites [28] Kim, A. et al. A mouse model of anemia of inflammation: complex pathogenesis with partial dependence on hepcidin. Blood 123, 1129–1136 (2014). source
- Not checked yetcites [29] Gardenghi, S. et al. Distinct roles for hepcidin and interleukin-6 in the recovery from anemia in mice injected with heat-killed Brucella abortus. Blood 123, 1137–1145 (2014). References 28 and 29 show that IL-6 and hepcidin are important but not exclusive mediators of anaemia of inflammation in a mouse model of severe anaemia induced by heat-killed bacteria. source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“Anaemia owing to ineffective erythropoiesis, as occurs most prominently in patients with β-thalassaemia, is associated with severe iron overload that develops even in the absence of blood transfusions but is exacerbated in patients who receive repeated transfusions36,37.”
§ Iron homeostasis in host defence and inflammation > Iron overload disorders and infections > Iron-loading anaemias
What the sources say
- Not checked yetcites [36] Musallam, K. M., Cappellini, M. D. & Taher, A. T. Iron overload in β-thalassemia intermedia: an emerging concern. Curr. Opin. Hematol. 20, 187–192 (2013). source
- Not checked yetcites [37] Maggio, A. et al. Iron chelation therapy in thalassemia major: a systematic review with meta-analyses of 1520 patients included on randomized clinical trials. Blood Cells Mol. Dis. 47, 166–175 (2011). source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“most studies suggest that NRAMP1 transports iron from phagosomes and other vacuoles that contain microorganisms to the cytoplasm of macrophages76–78, thereby starving vacuolar microorganisms of iron.”
§ Iron homeostasis in host defence and inflammation > Hepcidin-independent iron sequestration > Iron sequestration and host defence
What the sources say
- Not checked yetcites [76] Soe-Lin, S. et al. Nramp1 promotes efficient macrophage recycling of iron following erythrophagocytosis in vivo. Proc. Natl Acad. Sci. USA 106, 5960–5965 (2009). source
- Not checked yetcites [77] Cellier, M. F., Courville, P. & Campion, C. Nramp1 phagocyte intracellular metal withdrawal defense. Microbes Infect. 9, 1662–1670 (2007). source
- Not checked yetcites [78] Forbes, J. R. & Gros, P. Iron, manganese, and cobalt transport by Nramp1 (Slc11a1) and Nramp2 (Slc11a2) expressed at the plasma membrane. Blood 102, 1884–1892 (2003). 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
“S. Typhimurium elicits this response by a mechanism that is dependent on IL-6 and oestrogen-related receptor-γ (ESRRγ)88.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
What the sources say
- Not checked yetcites [88] Kim, D. K. et al. Inverse agonist of estrogen-related receptor γ controls Salmonella typhimurium infection by modulating host iron homeostasis. Nat. Med. 20, 419–424 (2014). 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
“In this way, these macrophages provide the bacteria with a source of iron from erythrophagocytosis and an M2 macrophage environment with attenuated antimicrobial mechanisms favouring the survival of the bacteria.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and erythrophagocytosis
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
“NRAMP1 expression is also stimulated by IFNγ72, and NRAMP1-mediated iron export from phagosomes containing intracellular microorganisms may help to counter the effect of systemic hepcidin.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
What the sources say
- Not checked yetcites [72] Canonne-Hergaux, F., Gruenheid, S., Govoni, G. & Gros, P. The Nramp1 protein and its role in resistance to infection and macrophage function. Proc. Assoc. Am. Physicians 111, 283–289 (1999). source
hedgedconditional- Asserted: passes — The authors put it forward as true.
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In the paper
“An effective iron chelator must be nontoxic, must have higher affinity for ferric iron than bacterial siderophores and must not be recognized by microbial siderophore transporters94.”
§ Iron homeostasis in host defence and inflammation > Therapeutic opportunities and challenges
What the sources say
- Not checked yetcites [94] Zhou, T., Ma, Y., Kong, X. & Hider, R. C. Design of iron chelators with therapeutic application. Dalton Trans. 41, 6371–6389 (2012). 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
“Iron deficiency is widespread in developing countries and is a major cause of chronic illness and loss of economic productivity56.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Tropical infections
What the sources say
- Not checked yetcites [56] Pasricha, S. R., Drakesmith, H., Black, J., Hipgrave, D. & Biggs, B. A. Control of iron deficiency anemia in low- and middle-income countries. Blood 121, 2607–2617 (2013). source
plaindirect- Asserted: passes — The authors put it forward as true.
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- Load-bearing: fails — The paper’s conclusions may not depend on it.
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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.
In the paper
“The uptake of transferrin by Neisseria species is specific to hominid transferrin, indicating that this specialized uptake mechanism facilitates their residence in the human host and several other hominids83.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Extracellular bacteria and host ferroproteins
What the sources say
- Not checked yetcites [83] Noinaj, N. et al. Structural basis for iron piracy by pathogenic Neisseria. Nature 483, 53–58 (2012). source
hedgeddirect- 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
“Nevertheless, these mice develop hypoferraemia, indicating that the nitric oxide-dependent mechanism operates at a local level and requires the presence of bacteria within the macrophage, leaving most iron-recycling macrophages under the dominant regulatory influence of hepcidin.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
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
“In this model, mini-hepcidins rapidly decreased iron concentrations in the plasma and extracellular fluid, and thereby decreased the concentrations of non-transferrin-bound iron, which is a likely source of iron for siderophilic bacteria.”
§ Iron homeostasis in host defence and inflammation > Therapeutic opportunities and challenges
What the sources say
- Not checked yetcites [52] Arezes, J. et al. Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus. Cell Host Microbe 17, 47–57 (2015). This study shows that hepcidin-deficient mice are rapidly killed by V. vulnificus , but mice can be saved by the administration of minihepcidin, demonstrating the protective effect of hypoferraemia. 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
“In chronic infection with S. Typhimurium, the bacteria may induce erythrophagocytosis and the conversion of hepatic and splenic macrophages into an M2 phenotype, a process that also requires host signals but has not been characterized in molecular detail93.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and erythrophagocytosis
What the sources say
- Not checked yetcites [93] Pilonieta, M. C., Moreland, S. M., English, C. N. & Detweiler, C. S. Salmonella enterica infection stimulates macrophages to hemophagocytose. mBio 5, e02211 (2014). 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
“Although the hepcidin–ferroportin system seems to function maladaptively during infections with intracellular microorganisms, this host response could be mitigated in infected macrophages by local mechanisms that counteract the systemic effects of hepcidin.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
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
“IL-6 is increased early in most microbial infections and it stimulates hepcidin transcription via the JAK2–STAT3 pathway in a manner dependent on STAT3-binding motifs in the promoter of HAMP (the hepcidin gene)89–91.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
What the sources say
- Not checked yetcites [89] Wrighting, D. M. & Andrews, N. C. Interleukin-6 induces hepcidin expression through STAT3. Blood 108, 3204–3209 (2006). source
- Not checked yetcites [90] Fleming, R. E. Hepcidin activation during inflammation: make it STAT. Gastroenterology 132, 447–449 (2007). source
- Not checked yetcites [91] Pietrangelo, A. et al. STAT3 is required for IL-6-gp130-dependent activation of hepcidin in vivo. Gastroenterology 132, 294–300 (2007). 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
“Despite several decades of research in this area that have yielded three successful drugs for the treatment of iron overload disorders, and evidence of in vitro microbistatic activity for several compounds95, no chelator has yet been adopted as an antimicrobial therapeutic.”
§ Iron homeostasis in host defence and inflammation > Therapeutic opportunities and challenges
What the sources say
- Not checked yetcites [95] Thompson, M. G., Corey, B. W., Si, Y., Craft, D. W. & Zurawski, D. V. Antibacterial activities of iron chelators against common nosocomial pathogens. Antimicrob. Agents Chemother. 56, 5419–5421 (2012). source
plain- 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
“A direct hepcidin-mediated anti-inflammatory effect mediated by ferroportin and the Janus kinase (JAK)–signal transducer and activator of transcription (STAT) pathway was proposed70, but JAK–STAT-mediated signalling by ferroportin was not confirmed in subsequent more-detailed studies71.”
§ Iron homeostasis in host defence and inflammation > Iron deficiency and host defence > Iron deficiency and inflammation
What the sources say
- Not checked yetcites [70] De Domenico, I. et al. Hepcidin mediates transcriptional changes that modulate acute cytokine-induced inflammatory responses in mice. J. Clin. Invest. 120, 2395–2405 (2010). source
- Not checked yetcites [71] Ross, S. L. et al. Molecular mechanism of hepcidin-mediated ferroportin internalization requires ferroportin lysines, not tyrosines or JAK-STAT. Cell Metab. 15, 905–917 (2012). source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Chemical inhibition of the ESRRγ pathway in a mouse model significantly decreased bacterial burden and modestly improved the survival of infected mice88.”
§ Iron homeostasis in host defence and inflammation > Microbial countermeasures > Intracellular microorganisms and the hepcidin–ferroportin system
What the sources say
- Not checked yetcites [88] Kim, D. K. et al. Inverse agonist of estrogen-related receptor γ controls Salmonella typhimurium infection by modulating host iron homeostasis. Nat. Med. 20, 419–424 (2014). 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
“Finally, the exquisite dependence of most microorganisms on iron provides a rationale for the design of new antimicrobials that target iron uptake mechanisms in pathogenic microorganisms.”
§ Iron homeostasis in host defence and inflammation > Conclusions and perspectives
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.
Probably not a substantial claim.
- Rests on an assumption: Most microorganisms depend exquisitely on iron.
The paper relies on this without support.
Most microorganisms depend absolutely on exogenous iron for survival.
“Given the absolute dependence of most microorganisms on exogenous iron for their survival, it has been assumed that the hypoferraemia of infection and inflammation has a host defence function.”
The paper relies on this without support.
Iron is essential for nearly all microorganisms.
“Iron is also essential for nearly all microorganisms, plants and invertebrate animals, in which it functions as a catalytic component of enzymes that mediate many redox reactions that are crucial for energy production and intermediary metabolism.”
The paper relies on this without support.
Non-transferrin-bound iron can amplify tissue injury by catalysing extracellular ROS production or by rapid cellular uptake causing iron overload and secondary ROS.
“Moreover, non-transferrin-bound iron can amplify tissue injury either because it catalyses the extracellular production of injurious reactive oxygen species (ROS) or because it is rapidly taken up some cell types, causing cellular iron overload with the secondary generation of ROS.”
The paper relies on this without support.
Malarial parasites require iron at both the liver and erythrocyte stages.
“The parasites require iron at both the liver and the erythrocyte stage.”
The paper relies on this without support.
Iron deficiency is endemic in tropical regions.
“The possibility that iron deficiency, which is endemic in tropical regions, may be protective against certain infections has also been raised.”
The paper relies on this without support.
Hepcidin acts on ferroportin to shift iron into macrophages.
“In addition to hepcidin — the effects of which on ferroportin cause redistribution of iron into macrophages —”
The paper relies on this without support.
Lactoferrin, unlike transferrin, keeps binding iron at the low pH found in inflamed and infected tissues.
“Lactoferrin is a homologue of the iron carrier protein transferrin but differs from transferrin by continuing to bind iron even at low pH, which is common in inflamed and infected tissues.”
The paper relies on this without support.
Siderocalin binds iron only when it is complexed with small natural organic chelators.
“Siderocalin, a member of a family of proteins that contain a pocket (calyx) for small mostly hydrophobic molecules, binds iron when it is complexed with small natural organic chelators.”
The paper relies on this without support.
Haptoglobin and haemopexin carry free haemoglobin and haem, respectively, to macrophages and hepatocytes for degradation.
“Haptoglobin and haemopexin are carrier proteins that transport free haemoglobin and haem, respectively, for degradation by macrophages and hepatocytes.”
The paper relies on this without support.
NRAMP1 is a ferrous iron transporter located in phagocytic vacuole membranes of macrophages and neutrophils.
“NRAMP1 is a ferrous iron transporter found in the membranes of phagocytic vacuoles of macrophages and neutrophils.”
The paper relies on this without support.
Red blood cells are by far the richest source of iron.
“Erythrocytes are by far the richest source of iron”
The paper relies on this without support.
Most microorganisms depend exquisitely on iron.
“the exquisite dependence of most microorganisms on iron”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“This is essential in limiting iron availability to invading pathogens, as both bacterial and fungal pathogens have been shown to target haem, hemoglobin, and other iron-complex proteins (Ganz and Nemeth, 2015).”
From Iron at the Centre of Candida albicans Interactions (2018) · cites this paper as Ganz and Nemeth, 2015
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Iron in the human host is largely unavailable as it is constantly sequestered by specialized proteins which prevent attack by ROS or exploitation by pathogens (Ganz and Nemeth, 2015).”
From Iron at the Centre of Candida albicans Interactions (2018) · cites this paper as Ganz and Nemeth, 2015
The cited source says what the claim attributes to it.
In the citing paper
“Systemic iron levels are tightly regulated by iron metabolism master regulator, hepcidin (encoded by HAMP), while individual cells may independently regulate iron by receptor-mediated endocytosis of transferrin (Ganz and Nemeth, 2015).”
From Iron at the Centre of Candida albicans Interactions (2018) · cites this paper as Ganz and Nemeth, 2015
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“In the adaptive immune system, iron is an essential growth-factor for the clonal expansion of lymphocyte subsets (Ganz and Nemeth, 2015;Soares and Weiss, 2015;Weiss, 2002).”
From Iron in infection and immunity (2020) · cites this paper as Ganz and Nemeth, 2015
Experimental — accuracy not yet measuredIn the citing paper
“Accordingly, iron trafficking is controlled by cytokines and acute phase proteins, whereas the metal itself promotes lymphocyte and macrophage differentiation, anti-microbial immune effector function, and immune cell metabolism, as we will discuss later (Ganz and Nemeth, 2015; Soares and Weiss, 2015).”
From The Role of Iron Regulation in Immunometabolism and Immune-Related Disease (2019) · cites this paper as Ganz and Nemeth, 2015
In the citing paper
“This process is blocked by the action of hepcidin during times of infection to prevent iron release in the circulation, which would otherwise fuel extracellular pathogen growth (Ganz and Nemeth, 2015).”
From The Role of Iron Regulation in Immunometabolism and Immune-Related Disease (2019) · cites this paper as Ganz and Nemeth, 2015
In the citing paper
“Macrophage iron metabolism and immune functions are interconnected [57, 79, 165, 247].”
From “Pumping iron”—how macrophages handle iron at the systemic, microenvironmental, and cellular levels (2017) · cites this paper as [79]
In the citing paper
“infection triggered macrophage iron retention as a host defense mechanism to withhold the nutrient iron from invading microbes [24,25,26]”
From Prevalence and Predictive Value of Anemia and Dysregulated Iron Homeostasis in Patients with COVID-19 Infection (2020) · cites this paper as [24]
In the citing paper
“In haemochromatosis, intestinal iron absorption is disconnected from systemic iron availability, resulting in potentially lethal iron loading and susceptibility to fatal siderophilic bacterial infections, which exemplify the importance of regulating intestinal iron absorption. 42 , 43”
From The battle for iron in enteric infections (2020) · cites this paper as [43]
In the citing paper
“This is circumvented by the recycling of the Fe contained in the heme groups of Hb inside RBC (14–16), achieved largely via the continuous engulfment and digestion of senescent or damaged RBC by erythrophagocytic macrophages (EM) in the red pulp of the spleen (15) (Figure 1).”
From Innate Nutritional Immunity (2018) · cites this paper as [16]
In the citing paper
“However, persistent chronic hypoferremia restricts iron availability for erythropoiesis (Ganz and Nemeth, 2015).”
From Pharmacological Targeting of the Hepcidin/Ferroportin Axis (2016) · cites this paper as Ganz and Nemeth, 2015
In the citing paper
“Therefore, the reduction of serum TF appears to be one of the mechanisms of microbial iron withdrawal [54–57].”
From Iron deficiency or anemia of inflammation?: Differential diagnosis and mechanisms of anemia of inflammation (2016) · cites this paper as [55]
Citations
Cites
Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients
Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,836
Nemeth, E., Rivera, S., Gabayan, V., Keller, C., Taudorf, S., Pedersen, B. K., & Ganz, T. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200420945 · Cited by 2,650
Self-citationLipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron
Flo, T. H., Smith, K. D., Sato, S., Rodriguez, D. J., Holmes, M. A., Strong, R. K., Akira, S., & Aderem, A. (2004) · Nature · doi:10.1038/nature03104 · Cited by 1,877
Nicolas, G., Chauvet, C., Viatte, L., Danan, J. L., Bigard, X., Devaux, I., Beaumont, C., Kahn, A., & Vaulont, S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215686 · Cited by 1,214
Iron in infection and immunity
Cassat, J. E., & Skaar, E. P. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.04.010 · Cited by 1,214
Identification of erythroferrone as an erythroid regulator of iron metabolism
Kautz, L., Jung, G., Valore, E. V., Rivella, S., Nemeth, E., & Ganz, T. (2014) · Nature Genetics · doi:10.1038/ng.2996 · Cited by 1,127
Self-citationGanz, T. (2013) · Physiological Reviews · doi:10.1152/physrev.00008.2013 · Cited by 1,122
Self-citationInterleukin-6 induces hepcidin expression through STAT3
Wrighting, D. M., & Andrews, N. C. (2006) · Blood · doi:10.1182/blood-2006-06-027631 · Cited by 983
Sazawal, S., Black, R. E., Ramsan, M., Chwaya, H. M., Stoltzfus, R. J., Dutta, A., Dhingra, U., Kabole, I., Deb, S., Othman, M. K., et al. (2006) · The Lancet · doi:10.1016/s0140-6736(06)67962-2 · Cited by 981
Iron and Its Relation to Immunity and Infectious Disease
Oppenheimer, S. J. (2001) · The Journal of Nutrition · doi:10.1093/jn/131.2.616s · Cited by 695
Cited by
Sorted by citations
Items 101–200 of 838
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Thind, M. K., Uhlig, H. H., Glogauer, M., Palaniyar, N., Bourdon, C., Gwela, A., Lancioni, C., Berkley, J. A., Bandsma, R., & Farooqui, A. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1334205 · Cited by 78
Understanding How Minerals Contribute to Optimal Immune Function
Ştefanache, A., Lungu, I. I., Butnariu, I.-A., Călin, G., Guțu, C., Marcu, C., Grierosu, C., Goroftei, E. R. B., Duceac, L.-D., Dabija, M. G., et al. (2023) · Journal of Immunology Research · doi:10.1155/2023/3355733 · Cited by 99
Tang, M., Frank, D. N., Sherlock, L. G., Ir, D., Robertson, C. E., & Krebs, N. F. (2016) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000001154 · Cited by 75
Siderophore-based biosensors and nanosensors; new approach on the development of diagnostic systems
Nosrati, R., Dehghani, S., Karimi, B., Yousefi, M., Taghdisi, S. M., Abnous, K., Alibolandi, M., & Ramezani, M. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.05.057 · Cited by 73
The role of iron homeostasis and iron-mediated ROS in cancer.
Ying, J., Lu, Z.-B., Fu, L., Tong, Y., Wang, Z., Li, W., & Mou, X. (2021) · PubMed · Cited by 85
Liver – master and servant of serum proteome
Kuscuoglu, D., Janciauskiene, S. M., Hamesch, K., Haybaeck, J., Trautwein, C., & Strnad, P. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2018.04.018 · Cited by 73
Post-transcriptional regulation of immune responses by RNA binding proteins
Mino, T., & Takeuchi, O. (2018) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.94.017 · Cited by 68
Yoshinaga, M., Nakatsuka, Y., Vandenbon, A., Ori, D., Uehata, T., Tsujimura, T., Suzuki, Y., Mino, T., & Takeuchi, O. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.009 · Cited by 68
Reddy, V. P., Chinta, K. C., Saini, V., Glasgow, J. N., Hull, T. D., Traylor, A., Rey-Stolle, F., Soares, M. P., Madansein, R., Rahman, M. A., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00860 · Cited by 69
Stefanova, D., Raychev, A., Deville, J., Humphries, R., Campeau, S., Ruchala, P., Nemeth, E., Ganz, T., & Bulut, Y. (2018) · Infection and Immunity · doi:10.1128/iai.00253-18 · Cited by 68
Self-citationBrandtner, A. K., Tymoszuk, P., Nairz, M., Lehner, G. F., Fritsche, G., Vales, A., Falkner, A., Schennach, H., Theurl, I., Joannidis, M., et al. (2020) · Journal of Intensive Care · doi:10.1186/s40560-020-00495-8 · Cited by 69
Greenham, G., Buckley, J. D., Garrett, J. M., Eston, R. G., & Norton, K. I. (2018) · Sports Medicine · doi:10.1007/s40279-018-0969-2 · Cited by 69
Armitage, A. E., & Moretti, D. (2019) · Pharmaceuticals · doi:10.3390/ph12020059 · Cited by 76
Hepcidin Deficiency Protects Against Atherosclerosis
Malhotra, R. K., Wunderer, F., Barnes, H. J., Bagchi, A., Buswell, M. D., O’Rourke, C., Slocum, C. L., Ledsky, C. D., Peneyra, K. M., Sigurslid, H. H., et al. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.312215 · Cited by 68
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Volkova, M. B., Atamas, A., Tsarenko, A., Rogachev, A. V., & Guskov, A. (2021) · Biomolecules · doi:10.3390/biom11040584 · Cited by 68
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Alam, M. Z., Devalaraja, S., & Haldar, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00033 · Cited by 72
Riedelberger, M., Penninger, P., Tscherner, M., Seifert, M., Jenull, S., Brunnhofer, C., Scheidl, B., Tsymala, I., Bourgeois, C., Petryshyn, A., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.01.023 · Cited by 64
Macrophage ferroportin is essential for stromal cell proliferation in wound healing
Recalcati, S., Gammella, E., Buratti, P., Doni, A., Anselmo, A., Locati, M., & Cairo, G. (2018) · Haematologica · doi:10.3324/haematol.2018.197517 · Cited by 68
Alam, Z., Devalaraja, S., Li, M., To, T. K. J., Folkert, I. W., Mitchell-Velasquez, E., Dang, M. T., Young, P. A., Wilbur, C. J., Silverman, M. A., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107825 · Cited by 64
Anemia, iron, and HIV: decoding the interconnected pathways: A review
Obeagu, E. I., Obeagu, G. U., Ukibe, N. R., & Oyebadejo, S. A. (2024) · Medicine · doi:10.1097/md.0000000000036937 · Cited by 77
Association between iron status and the risk of adverse outcomes in COVID-19
Lv, Y., Chen, L., Liang, X., Liu, X., Gao, M., Wang, Q., Wei, Q., & Liu, L. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.11.033 · Cited by 61
Iron–sulfur clusters as inhibitors and catalysts of viral replication
Ebrahimi, K. H., Ciofi‐Baffoni, S., Hagedoorn, P., Nicolet, Y., Brun, N. E. L., Hagen, W. R., & Armstrong, F. A. (2022) · Nature Chemistry · doi:10.1038/s41557-021-00882-0 · Cited by 63
Therapeutic Advances in Regulating the Hepcidin/Ferroportin Axis
Hawula, Z. J., Wallace, D. F., Subramaniam, V. N., & Rishi, G. (2019) · Pharmaceuticals · doi:10.3390/ph12040170 · Cited by 62
Bertolla, M., Cenci, L., Anesi, A., Ambrosi, E., Tagliaro, F., Vanzetti, L., Guella, G., & Bossi, A. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b16291 · Cited by 64
The battle for iron in enteric infections
Sousa Gerós, A., Simmons, A., Drakesmith, H., Aulicino, A., & Frost, J. N. (2020) · Immunology · doi:10.1111/imm.13236 · Cited by 58
From Host Heme To Iron: The Expanding Spectrum of Heme Degrading Enzymes Used by Pathogenic Bacteria
Lyles, K. V. M., & Eichenbaum, Z. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00198 · Cited by 63
Safety and benefits of antenatal oral iron supplementation in low‐income countries: a review
Mwangi, M., Prentice, A., & Verhoef, H. (2017) · British Journal of Haematology · doi:10.1111/bjh.14584 · Cited by 57
Smoking-induced iron dysregulation in the lung
Zhang, W. Z., Butler, J. J., & Cloonan, S. M. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.07.024 · Cited by 62
Ingestion, Immunity, and Infection: Nutrition and Viral Respiratory Tract Infections
Govers, C., Calder, P. C., Savelkoul, H. F. J., Albers, R., & van Neerven, R. J. J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.841532 · Cited by 71
Hecht‐Höger, A. M., Braun, B. C., Krause, E., Meschede, A., Krahe, R., Voigt, C. C., Greenwood, A. D., & Czirják, G. Á. (2020) · Molecular Ecology · doi:10.1111/mec.15437 · Cited by 42
Sun, J., Zhang, N., Xu, R.-C., Zhang, G., Liu, Z., Abuduwaili, W., Wang, F., Yu, X., Shi, X., Song, G., et al. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-03034-7 · Cited by 60
Iron acquisition in the cystic fibrosis lung and potential for novel therapeutic strategies
Tyrrell, J., & Callaghan, M. (2016) · Microbiology · doi:10.1099/mic.0.000220 · Cited by 56
Tarifeño-Saldivia, E., Aguilar, A., Contreras, D., Mercado, L. A., Lange, B. M., Márquez, K., Henríquez, A., Riquelme-Vidal, C., & Boltaña, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01296 · Cited by 59
Zhang, V., Nemeth, E., & Kim, A. (2019) · Pharmaceuticals · doi:10.3390/ph12010030 · Cited by 57
Self-citationNanomaterial-Based Repurposing of Macrophage Metabolism and Its Applications
Meng, T., He, D., Han, Z., Shi, R., Wang, Y., Ren, B., Zhang, C., Mao, Z., Luo, G., & Deng, J. (2024) · Nano-Micro Letters · doi:10.1007/s40820-024-01455-9 · Cited by 63
Iron Handling in Tumor-Associated Macrophages—Is There a New Role for Lipocalin-2?
Jung, M., Weigert, A., Mertens, C., Rehwald, C., & Brüne, B. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01171 · Cited by 54
Hematological disorders and pulmonary hypertension
Mathew, R., Huang, J. L., WU, J. M., Fallon, J. T., & Gewitz, M. H. (2016) · World Journal of Cardiology · doi:10.4330/wjc.v8.i12.703 · Cited by 53
Viral Hepatitis and Iron Dysregulation: Molecular Pathways and the Role of Lactoferrin
Mancinelli, R., Rosa, L., Cutone, A., Lepanto, M. S., Franchitto, A., Onori, P., Gaudio, E., & Valenti, P. (2020) · Molecules · doi:10.3390/molecules25081997 · Cited by 56
Ferroptosis: A New Promising Target for Lung Cancer Therapy
Xiong, R., He, R., Liu, B., Jiang, W., Wang, B., Li, N., & Geng, Q. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8457521 · Cited by 57
Spatial IMA1 regulation restricts root iron acquisition on MAMP perception
Cao, M., Platre, M. P., Tsai, H.-H. M., Zhang, L., Nobori, T., Armengot, L., Chen, Y., He, W., Brent, L., Coll, N. S., et al. (2024) · Nature · doi:10.1038/s41586-023-06891-y · Cited by 55
Huo, M., Tang, Z., Wang, L., Zhang, L., Guo, H., Chen, Y., Gu, P., & Shi, J. (2022) · Nature Communications · doi:10.1038/s41467-022-35503-y · Cited by 55
Kao, J., Wang, S., Ho, L.-W., Huang, S.-W., Chang, S.-H., Yang, R.-C., Ke, Y., Wu, C., Wang, J., & Shieh, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0156713 · Cited by 55
Kırmızı, D. A., Başer, E., Türksoy, V. A., Kara, M., Yalvaç, S., & Göçmen, A. Y. (2020) · Biological Trace Element Research · doi:10.1007/s12011-020-02220-w · Cited by 63
On the physiological and cellular homeostasis of ascorbate
Przybyło, M., & Langner, M. (2020) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-020-00223-y · Cited by 53
Sharma, G., Sharma, A., Kim, I., Gon, D., Kim, S., Park, E. S., Noh, J. G., Lee, J.-H., Ku, J. H., Choi, Y. H., et al. (2024) · Nature Immunology · doi:10.1038/s41590-024-01816-x · Cited by 58
Iron overload inhibits BMP/SMAD and IL-6/STAT3 signaling to hepcidin in cultured hepatocytes
Charlebois, E., & Pantopoulos, K. (2021) · PLoS ONE · doi:10.1371/journal.pone.0253475 · Cited by 51
Prophylactic Iron Supplementation in Pregnancy: A Controversial Issue
Friedrisch, J. R., & Friedrisch, B. K. (2017) · Biochemistry Insights · doi:10.1177/1178626417737738 · Cited by 57
Cytosolic Iron-Sulfur Assembly Is Evolutionarily Tuned by a Cancer-Amplified Ubiquitin Ligase
Weon, J. L., Yang, S. W., & Potts, P. R. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.11.010 · Cited by 49
Dietary diversity and poverty as risk factors for leprosy in Indonesia: A case-control study
Oktaria, S., Hurif, N. S., Naim, W., Thio, H. B., Nijsten, T. E. C., & Richardus, J. H. (2018) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006317 · Cited by 48
Guo, S., Frazer, D. M., & Anderson, G. J. (2016) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000285 · Cited by 49
Dichtl, S., Demetz, E., Haschka, D., Tymoszuk, P., Petzer, V., Nairz, M., Seifert, M., Hoffmann, A., Brigo, N., Würzner, R., et al. (2019) · mBio · doi:10.1128/mbio.02624-18 · Cited by 50
Heme-iron acquisition in fungi
Roy, U., & Kornitzer, D. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.05.006 · Cited by 46
de Oliveira, J., Denadai, M. B., & Costa, D. L. (2022) · Antioxidants · doi:10.3390/antiox11050861 · Cited by 54
Nutraceuticals and Dietary Supplements for Older Adults with Long COVID-19
Tosato, M., Ciciarello, F., Zazzara, M. B., Pais, C., Savera, G., Picca, A., Galluzzo, V., Coelho‐Júnior, H. J., Calvani, R., Marzetti, E., et al. (2022) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2022.04.004 · Cited by 51
Molecular mechanisms of ferroptosis and their role in inflammation
Wang, F., He, J., Xing, R., Sha, T., & Sun, B. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.2016739 · Cited by 50
Remodeling Macrophages by an Iron Nanotrap for Tumor Growth Suppression
Sang, Y., Deng, Q., Cao, F., Liu, Z., You, Y., Liu, H., Ren, J., & Qu, X. (2021) · ACS Nano · doi:10.1021/acsnano.1c05392 · Cited by 47
Wei, X., Babu, V. S., Lin, L., Hu, Y., Zhang, Y., Liu, X., Su, J., Li, J., Zhao, L., & Yuan, G. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.02.023 · Cited by 50
Figueiredo, M. P., Cunha, V. R. R., Leroux, F., et al. (2018) · ACS Omega · doi:10.1021/acsomega.8b02532 · Cited by 48
Li, Z., Lillehoj, H. S., Gadde, U. D., Ritter, D., & Oh, S. (2017) · Avian Diseases · doi:10.1637/11507-093016-reg.1 · Cited by 46
Grisouard, J., Li, S., Kubovčáková, L., Rao, T. N., Meyer, S. C., Lundberg, P., Hao-Shen, H., Romanet, V., Murakami, M., Radimerski, T., et al. (2016) · Blood · doi:10.1182/blood-2015-12-689216 · Cited by 50
Boukerb, A. M., Cambronel, M., Rodrigues, S., Mesguida, O., Knowlton, R., Feuilloley, M. G. J., Zommiti, M., & Connil, N. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.690942 · Cited by 47
Lunová, M., Schwarz, P., Nuraldeen, R., Levada, K. V., Kuscuoglu, D., Stützle, M., Spasić, M. V., Haybaeck, J., Ruchala, P. P., Jirsa, M., et al. (2016) · The Journal of Pathology · doi:10.1002/path.4822 · Cited by 44
Singh, K. S., Leu, J. I.-J., Barnoud, T., Vonteddu, P., Gnanapradeepan, K., Lin, C., Liu, Q., Barton, J. C., Kossenkov, A. V., George, D. L., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14151-9 · Cited by 45
McCormick, B., Murray‐Kolb, L. E., Lee, G. O., Schulze, K. J., Ross, A. C., Bauck, A., Lima, A. Â. M., Maciel, B. L. L., Kosek, M. N., Seidman, J. C., et al. (2019) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqz151 · Cited by 44
Zafar, N., & Khan, M. A. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734642 · Cited by 46
Lanser, L., Burkert, F. R., Bellmann‐Weiler, R., Schroll, A., Wildner, S. M., Fritsche, G., & Weiß, G. (2021) · Metabolites · doi:10.3390/metabo11100653 · Cited by 46
Dendritic Cells Modulate Iron Homeostasis and Inflammatory Abilities Following Quercetin Exposure
Galleggiante, V., Santis, S. D., Cavalcanti, E., Scarano, A., Benedictis, M. D., Serino, G., Caruso, M. L., Mastronardi, M., Pinto, A., Campiglia, P., et al. (2017) · Current Pharmaceutical Design · doi:10.2174/1381612823666170112125355 · Cited by 44
Pathways of heme utilization in fungi
Kornitzer, D., & Roy, U. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118817 · Cited by 44
Nairz, M., Schroll, A., Haschka, D., Dichtl, S., Tymoszuk, P., Demetz, E., Moser, P., Haas, H., Fang, F. C., Theurl, I., et al. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00110 · Cited by 46
Control of nutrient uptake by IRF4 orchestrates innate immune memory
Santosa, E. K., Kim, H., Rückert, T., Luduec, J.-B. L., Abbasi, A. J., Wingert, C. K., Peters, L., Frost, J. N., Hsu, K. C., Romagnani, C., et al. (2023) · Nature Immunology · doi:10.1038/s41590-023-01620-z · Cited by 40
Wang, M., Nie, Y., & Wu, X. (2020) · The ISME Journal · doi:10.1038/s41396-020-00800-1 · Cited by 42
Nurmi, K., Kareinen, I., Virkanen, J., Rajamäki, K., Kouri, V., Vaali, K., Levonen, A., Fyhrquist, N., Matikainen, S., Kovanen, P. T., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000448894 · Cited by 44
Sun, Y., Liu, M., Sun, W., Tang, X., Zhou, Y., Zhang, J., & Yang, B. J. (2024) · Advanced Materials · doi:10.1002/adma.202405002 · Cited by 47
Mohus, R. M., Paulsen, J., Gustad, L. T., Askim, Å., Mehl, A., DeWan, A. T., Afset, J. E., Åsvold, B. O., Solligård, E., & Damås, J. K. (2018) · Intensive Care Medicine · doi:10.1007/s00134-018-5320-8 · Cited by 44
Platre, M. P., Satbhai, S. B., Brent, L., Gleason, M. F., Cao, M., Grison, M., Glavier, M., Zhang, L., Gaillochet, C., Goeschl, C., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32167-6 · Cited by 46
Microbiota-assisted iron uptake promotes immune tolerance in the intestine
Zhu, L., Li, G., Liang, Z., Qi, T., Deng, K., Yu, J., Peng, Y., Zheng, J., Song, Y., & Chang, X. (2023) · Nature Communications · doi:10.1038/s41467-023-38444-2 · Cited by 47
Host-Pathogen Interaction as a Novel Target for Host-Directed Therapies in Tuberculosis
Abreu, R. B., Giri, P. K., & Quinn, F. D. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01553 · Cited by 44
Prenatal iron exposure and childhood type 1 diabetes
Størdal, K., McArdle, H. J., Hayes, H. E., Tapia, G., Viken, M. K., Lund‐Blix, N. A., Haugen, M. A., Joner, G., Skrivarhaug, T., Mårild, K., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-27391-4 · Cited by 43
Nanoparticles weaponized with built‐in functions for imaging‐guided cancer therapy
Jing, L., Yang, C., Zhang, P., Zeng, J., Li, Z., & Gao, M. (2020) · Open Research (University of Surrey) · doi:10.1002/viw2.19 · Cited by 42
Wu, A., Tymoszuk, P., Haschka, D., Heeke, S., Dichtl, S., Petzer, V., Seifert, M., Hilbe, R., Sopper, S., Talasz, H., et al. (2017) · Infection and Immunity · doi:10.1128/iai.00418-17 · Cited by 39
Targeting metabolic dysfunction of CD8 T cells and natural killer cells in cancer
Viel, S., Vivier, É., Walzer, T., & Marçais, A. (2024) · Nature Reviews Drug Discovery · doi:10.1038/s41573-024-01098-w · Cited by 53
Impact of Micronutrients on the Immune Response of Animals
Smith, A. D., Panickar, K. S., Urban, J. F., & Dawson, H. D. (2018) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-022516-022914 · Cited by 45
Iron Deprivation Induces Transcriptional Regulation of Mitochondrial Biogenesis
Rensvold, J. W., Krautkramer, K. A., Dowell, J. A., Denu, J. M., & Pagliarini, D. J. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.727701 · Cited by 43
The role of iron metabolism in cancer therapy focusing on tumor‐associated macrophages
Dong, D., Zhang, G., Yang, J., Zhao, B., Wang, S., Wang, L., Zhang, G., & Shang, P. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27569 · Cited by 37
Sorribes-Dauden, R., Peris, D., Martínez‐Pastor, M. T., & Puig, S. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.10.044 · Cited by 39
Present and Future of Siderophore-Based Therapeutic and Diagnostic Approaches in Infectious Diseases
Tonziello, G., Caraffa, E., Pinchera, B., Granata, G., & Petrosillo, N. (2019) · Infectious Disease Reports · doi:10.4081/idr.2019.8208 · Cited by 40
Established and Emerging Concepts to Treat Imbalances of Iron Homeostasis in Inflammatory Diseases
Petzer, V., Theurl, I., & Weiß, G. (2018) · Pharmaceuticals · doi:10.3390/ph11040135 · Cited by 41
Pulmonary Iron Homeostasis in Hepcidin Knockout Mice
Deschemin, J., Mathieu, J. R. R., Zumerle, S., Peyssonnaux, C., & Vaulont, S. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00804 · Cited by 41
Controversies on the Consequences of Iron Overload and Chelation in MDS
Vinchi, F., Hell, S., & Platzbecker, U. (2020) · HemaSphere · doi:10.1097/hs9.0000000000000357 · Cited by 43
Mu, M., Liang, X., Zhao, N., et al. (2023) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2022.09.003 · Cited by 41
Iron deficiency, pregnancy, and neonatal development
Ataíde, R., Fielding, K., Pasricha, S., & Bennett, C. (2023) · International Journal of Gynecology & Obstetrics · doi:10.1002/ijgo.14944 · Cited by 39
Hurrell, B. P., Sakano, Y., Shen, S. M.-C., Helou, D. G., Li, M., Shafiei-Jahani, P., Kazemi, M. H., Sakano, K., Li, X., Quach, C., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adk4728 · Cited by 42
Iron homeostasis and neurodegeneration in the ageing brain: Insight into ferroptosis pathways
Alrouji, M., Anwar, S., Venkatesan, K., Shahwan, M. J., Hassan, M. I., Islam, A., & Shamsi, A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102575 · Cited by 45
Mulens‐Arias, V., Rojas, J. M., & Barber, D. F. (2020) · Nanomaterials · doi:10.3390/nano10050837 · Cited by 39
Hoeft, K., Bloch, D. B., Graw, J. A., Malhotra, R. K., Ichinose, F., & Bagchi, A. (2017) · Anesthesiology · doi:10.1097/aln.0000000000001653 · Cited by 41
Hematopoietic niches, erythropoiesis and anemia of chronic infection
Gomes, A. C., & Gomes, M. S. (2015) · Experimental Hematology · doi:10.1016/j.exphem.2015.11.007 · Cited by 38
Blood Trace Element Concentrations in Polycystic Ovary Syndrome: Systematic Review and Meta-analysis
Spritzer, P. M., Lecke, S. B., Fabris, V. C., Ziegelmann, P. K., & Amaral, L. (2016) · Biological Trace Element Research · doi:10.1007/s12011-016-0774-4 · Cited by 36
Microbial Community Composition Impacts Pathogen Iron Availability during Polymicrobial Infection
Stacy, A., Abraham, N., Jorth, P. A., & Whiteley, M. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1006084 · Cited by 43
Wang, C., Wang, X., Song, G., Xing, H., Yang, L., Han, K., & Chang, Y. (2020) · Journal of Food Biochemistry · doi:10.1111/jfbc.13578 · Cited by 31
Metadata
- Authors
- Ganz, T., & Nemeth, E.
- Affiliations
- University of California, Los Angeles (US)
- University of California System (US)
- Corresponding author
- Ganz, Tomas
- Venue
- Nature Reviews Immunology
- Published
- 2015-07-10
- Volume
- 15
- Issue
- 8
- Pages
- 500-510
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC4801113
- OpenAlex
- W1570067866
- Cited by
- 843
- References
- 100
- Citations by year
- 2026: 89 · 2025: 78 · 2024: 90 · 2023: 75 · 2022: 103 · 2021: 81 · 2020: 82 · 2019: 63 · 2018: 69 · 2017: 58 · 2016: 47 · 2015: 7
- FWCI
- 9.02
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- CYTED Ciencia y Tecnología para el Desarrollo
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK107309)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Ferroptosis and cancer prognosis
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Keywords
- iron homeostasis, nutritional immunity, host defense, inflammation, iron limitation, infection, macrophages, cytokine production
- MeSH terms
- Animals, Bacterial Infections, Gene Expression Regulation, Homeostasis, Humans, Immunity, Innate, Inflammation, Iron, Macrophages, Signal Transduction, Cytokines, Nonheme Iron Proteins, Iron-Binding Proteins, Iron-Regulatory Proteins
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