Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 46

The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.

Nutritional Modulation of the Microbiome and Immune Response

Burr, Ansen H P, Bhattacharjee, Amrita, Hand, Timothy W·2020·The Journal of Immunology
DOI 10.4049/jimmunol.2000419
Open this paper in CoChat — free account

Abstract

The evolution of the immune system, diet, and the microbiome are interconnected. Dietary metabolites modulate the cells of the immune system both directly and indirectly via shifts in the composition of the intestinal microbiota and its products. As a result, overconsumption and malnutrition can have substantial effects on immune responses and inflammation. In resource-rich nations, diets high in processed foods, fat, and sugar can contribute to chronic inflammatory conditions, which are on the rise worldwide. Conversely, in resource-poor countries, malnutrition associated with food insecurity can lead to immunodeficiencies and shifts in the microbiome that drive intestinal inflammation. Developing a deeper understanding of the relationship between diet, microbiota, and the immune system is of huge importance, given its impact on inflammatory diseases and its potential as an easily modifiable mediator of immunomodulation.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.4049/jimmunol.2000419

Cites

34 of 34 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Research works printed but not linked: 116

  1. Romano, 2017, Gut microbiota as a trigger of accelerated directional adaptive evolution: acquisition of herbivory in the context of extracellular vesicles, microRNAs and inter-kingdom crosstalk, Front. Microbiol., 8, 721, 10.3389/fmicb.2017.00721 · DOI
  2. Kostic, 2013, Exploring host-microbiota interactions in animal models and humans, Genes Dev., 27, 701, 10.1101/gad.212522.112 · DOI · Paper page
  3. McFall-Ngai, 2007, Adaptive immunity: care for the community, Nature, 445, 153, 10.1038/445153a · DOI · Paper page
  4. Belkaid, 2014, Role of the microbiota in immunity and inflammation, Cell, 157, 121, 10.1016/j.cell.2014.03.011 · DOI · Paper page
  5. Gersh, 2010, Novel therapeutic concepts: the epidemic of cardiovascular disease in the developing world: global implications, Eur. Heart J., 31, 642, 10.1093/eurheartj/ehq030 · DOI · Paper page
  6. Cordain, 2005, Origins and evolution of the Western diet: health implications for the 21st century, Am. J. Clin. Nutr., 81, 341, 10.1093/ajcn.81.2.341 · DOI · Paper page
  7. Flegal, 1998, Overweight and obesity in the United States: prevalence and trends, 1960-1994, Int. J. Obes. Relat. Metab. Disord., 22, 39, 10.1038/sj.ijo.0800541 · DOI · Paper page
  8. Ogden, 2014, Prevalence of childhood and adult obesity in the United States, 2011-2012, JAMA, 311, 806, 10.1001/jama.2014.732 · DOI · Paper page
  9. Chandra, 1981, Immune response in overnutrition, Cancer Res., 41, 3795
  10. Daryabor, 2019, An update on immune dysregulation in obesity-related insulin resistance, Scand. J. Immunol., 89, 10.1111/sji.12747 · DOI
  11. Kanneganti, 2012, Immunological complications of obesity, Nat. Immunol., 13, 707, 10.1038/ni.2343 · DOI · Paper page
  12. Bleau, 2015, Crosstalk between intestinal microbiota, adipose tissue and skeletal muscle as an early event in systemic low-grade inflammation and the development of obesity and diabetes, Diabetes Metab. Res. Rev., 31, 545, 10.1002/dmrr.2617 · DOI
  13. Woodland, 2016, Short-term high-fat feeding induces islet macrophage infiltration and β-cell replication independently of insulin resistance in mice, Am. J. Physiol. Endocrinol. Metab., 311, E763, 10.1152/ajpendo.00092.2016 · DOI
  14. Okumura, 2017, Roles of intestinal epithelial cells in the maintenance of gut homeostasis, Exp. Mol. Med., 49, 10.1038/emm.2017.20 · DOI · Paper page
  15. Amar, 2011, Intestinal mucosal adherence and translocation of commensal bacteria at the early onset of type 2 diabetes: molecular mechanisms and probiotic treatment, EMBO Mol. Med., 3, 559, 10.1002/emmm.201100159 · DOI · Paper page
  16. Cani, 2008, Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice, Diabetes, 57, 1470, 10.2337/db07-1403 · DOI · Paper page
  17. Amar, 2008, Energy intake is associated with endotoxemia in apparently healthy men, Am. J. Clin. Nutr., 87, 1219, 10.1093/ajcn/87.5.1219 · DOI · Paper page
  18. Beyaz, 2016, High-fat diet enhances stemness and tumorigenicity of intestinal progenitors. [Published erratum appears in 2018 Nature 560: E26.], Nature, 531, 53, 10.1038/nature17173 · DOI · Paper page
  19. Kawano, 2016, Colonic pro-inflammatory macrophages cause insulin resistance in an intestinal Ccl2/Ccr2-dependent manner, Cell Metab., 24, 295, 10.1016/j.cmet.2016.07.009 · DOI
  20. Shi, 2006, TLR4 links innate immunity and fatty acid-induced insulin resistance, J. Clin. Invest., 116, 3015, 10.1172/JCI28898 · DOI · Paper page
  21. Wen, 2011, Fatty acid-induced NLRP3-ASC inflammasome activation interferes with insulin signaling, Nat. Immunol., 12, 408, 10.1038/ni.2022 · DOI · Paper page
  22. Kim, 2012, High fat diet-induced gut microbiota exacerbates inflammation and obesity in mice via the TLR4 signaling pathway, PLoS One, 7
  23. Yoshida, 2001, Fatty acids enhance GRO/CINC-1 and interleukin-6 production in rat intestinal epithelial cells, J. Nutr., 131, 2943, 10.1093/jn/131.11.2943 · DOI
  24. Luck, 2015, Regulation of obesity-related insulin resistance with gut anti-inflammatory agents, Cell Metab., 21, 527, 10.1016/j.cmet.2015.03.001 · DOI · Paper page
  25. Burcelin, 2012, Immuno-microbiota cross and talk: the new paradigm of metabolic diseases, Semin. Immunol., 24, 67, 10.1016/j.smim.2011.11.011 · DOI
  26. Hermetet, 2019, High-fat diet disturbs lipid raft/TGF-β signaling-mediated maintenance of hematopoietic stem cells in mouse bone marrow, Nat. Commun., 10, 523, 10.1038/s41467-018-08228-0 · DOI
  27. Haghikia, 2015, Dietary fatty acids directly impact central nervous system autoimmunity via the small intestine. [Published erratum appears in 2016 Immunity 44: 951–953.], Immunity, 43, 817, 10.1016/j.immuni.2015.09.007 · DOI · Paper page
  28. Zhang, 2012, Structural resilience of the gut microbiota in adult mice under high-fat dietary perturbations, ISME J., 6, 1848, 10.1038/ismej.2012.27 · DOI · Paper page
  29. Le Chatelier, 2013, Richness of human gut microbiome correlates with metabolic markers, Nature, 500, 541, 10.1038/nature12506 · DOI · Paper page
  30. Turnbaugh, 2006, An obesity-associated gut microbiome with increased capacity for energy harvest, Nature, 444, 1027, 10.1038/nature05414 · DOI · Paper page
  31. Turnbaugh, 2008, Diet-induced obesity is linked to marked but reversible alterations in the mouse distal gut microbiome, Cell Host Microbe, 3, 213, 10.1016/j.chom.2008.02.015 · DOI · Paper page
  32. Everard, 2013, Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity, Proc. Natl. Acad. Sci. USA, 110, 9066, 10.1073/pnas.1219451110 · DOI · Paper page
  33. de La Serre, 2010, Propensity to high-fat diet-induced obesity in rats is associated with changes in the gut microbiota and gut inflammation, Am. J. Physiol. Gastrointest. Liver Physiol., 299, G440, 10.1152/ajpgi.00098.2010 · DOI · Paper page
  34. Las Heras, 2019, Short-term consumption of a high-fat diet increases host susceptibility to Listeria monocytogenes infection, Microbiome, 7, 7, 10.1186/s40168-019-0621-x · DOI
  35. Monteiro, 2013, Ultra-processed products are becoming dominant in the global food system, Obes. Rev., 14, 21, 10.1111/obr.12107 · DOI · Paper page
  36. Johnson, 2007, Potential role of sugar (fructose) in the epidemic of hypertension, obesity and the metabolic syndrome, diabetes, kidney disease, and cardiovascular disease, Am. J. Clin. Nutr., 86, 899, 10.1093/ajcn/86.4.899 · DOI · Paper page
  37. Bergheim, 2008, Antibiotics protect against fructose-induced hepatic lipid accumulation in mice: role of endotoxin, J. Hepatol., 48, 983, 10.1016/j.jhep.2008.01.035 · DOI · Paper page
  38. Freemerman, 2014, Metabolic reprogramming of macrophages: glucose transporter 1 (GLUT1)-mediated glucose metabolism drives a proinflammatory phenotype, J. Biol. Chem., 289, 7884, 10.1074/jbc.M113.522037 · DOI · Paper page
  39. Gerriets, 2015, Metabolic programming and PDHK1 control CD4+ T cell subsets and inflammation, J. Clin. Invest., 125, 194, 10.1172/JCI76012 · DOI · Paper page
  40. Palmer, 2015, Glucose metabolism regulates T cell activation, differentiation, and functions, Front. Immunol., 6, 1, 10.3389/fimmu.2015.00001 · DOI · Paper page
  41. Thwe, 2017, Cell-Intrinsic glycogen metabolism supports early glycolytic reprogramming required for dendritic cell immune responses. [Published erratum appears in 2019 Cell Metab. 30: 225.], 558
  42. Delgoffe, 2015, Sugar, fat, and protein: new insights into what T cells crave, Curr. Opin. Immunol., 33, 49, 10.1016/j.coi.2015.01.015 · DOI
  43. Zhang, 2019, High glucose intake exacerbates autoimmunity through reactive-oxygen-species-mediated TGF-β cytokine activation, 671
  44. Gerriets, 2016, Foxp3 and toll-like receptor signaling balance Treg cell anabolic metabolism for suppression, Nat. Immunol., 17, 1459, 10.1038/ni.3577 · DOI · Paper page
  45. Suskind, 2016, Patients perceive clinical benefit with the specific carbohydrate diet for inflammatory bowel disease, Dig. Dis. Sci., 61, 3255, 10.1007/s10620-016-4307-y · DOI
  46. Caro-Maldonado, 2014, Metabolic reprogramming is required for antibody production that is suppressed in anergic but exaggerated in chronically BAFF-exposed B cells, J. Immunol., 192, 3626, 10.4049/jimmunol.1302062 · DOI · Paper page
  47. Angiari, 2020, Pharmacological activation of pyruvate kinase M2 inhibits CD4 + T cell pathogenicity and suppresses autoimmunity, 391
  48. Kamada, 2012, Regulated virulence controls the ability of a pathogen to compete with the gut microbiota, Science, 336, 1325, 10.1126/science.1222195 · DOI · Paper page
  49. Mohan, 2009, Salt and high blood pressure, Clin. Sci. (Lond.), 117, 1, 10.1042/CS20080207 · DOI
  50. Heikamp, 2014, The AGC kinase SGK1 regulates TH1 and TH2 differentiation downstream of the mTORC2 complex, Nat. Immunol., 15, 457, 10.1038/ni.2867 · DOI
  51. Tubbs, 2017, Dietary salt exacerbates experimental colitis, J. Immunol., 199, 1051, 10.4049/jimmunol.1700356 · DOI
  52. Sonnenburg, 2014, Starving our microbial self: the deleterious consequences of a diet deficient in microbiota-accessible carbohydrates, Cell Metab., 20, 779, 10.1016/j.cmet.2014.07.003 · DOI · Paper page
  53. Flint, 2012, The role of the gut microbiota in nutrition and health, Nat. Rev. Gastroenterol. Hepatol., 9, 577, 10.1038/nrgastro.2012.156 · DOI · Paper page
  54. Ng, 2019, Recovery of the gut microbiota after antibiotics depends on host diet, community context, and environmental reservoirs, 650
  55. Byndloss, 2017, Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion, Science, 357, 570, 10.1126/science.aam9949 · DOI · Paper page
  56. Roediger, 1992, Oxidative and synthetic functions of n-butyrate in colonocytes, Dis. Colon Rectum, 35, 511, 10.1007/BF02049412 · DOI
  57. Maslowski, 2009, Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43, Nature, 461, 1282, 10.1038/nature08530 · DOI · Paper page
  58. Trompette, 2018, Dietary fiber confers protection against Flu by shaping Ly6c - patrolling monocyte hematopoiesis and CD8 + T cell metabolism, 992
  59. Arpaia, 2013, Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation, Nature, 504, 451, 10.1038/nature12726 · DOI · Paper page
  60. Furusawa, 2013, Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. [Published erratum appears in 2014 Nature 506: 254.], Nature, 504, 446, 10.1038/nature12721 · DOI · Paper page
  61. Smith, 2013, The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis, Science, 341, 569, 10.1126/science.1241165 · DOI · Paper page
  62. Iweala, 2019, The microbiome and food allergy, Annu. Rev. Immunol., 37, 377, 10.1146/annurev-immunol-042718-041621 · DOI
  63. Tan, 2016, Dietary fiber and bacterial SCFA enhance oral tolerance and protect against food allergy through diverse cellular pathways, Cell Rep., 15, 2809, 10.1016/j.celrep.2016.05.047 · DOI · Paper page
  64. Wu, 2017, Microbiota metabolite short-chain fatty acid acetate promotes intestinal IgA response to microbiota which is mediated by GPR43, Mucosal Immunol., 10, 946, 10.1038/mi.2016.114 · DOI · Paper page
  65. Sanchez, 2020, B cell-intrinsic epigenetic modulation of antibody responses by dietary fiber-derived short-chain fatty acids, Nat. Commun., 11, 60, 10.1038/s41467-019-13603-6 · DOI · Paper page
  66. Silva, 2015, A high-glycemic index, low-fiber breakfast affects the postprandial plasma glucose, insulin, and ghrelin responses of patients with type 2 diabetes in a randomized clinical trial, J. Nutr., 145, 736, 10.3945/jn.114.195339 · DOI · Paper page
  67. Soare, 2014, The effect of the macrobiotic Ma-Pi 2 diet vs. the recommended diet in the management of type 2 diabetes: the randomized controlled MADIAB trial, Nutr. Metab. (Lond.), 11, 39, 10.1186/1743-7075-11-39 · DOI
  68. Li, 2011, Exogenous stimuli maintain intraepithelial lymphocytes via aryl hydrocarbon receptor activation, Cell, 147, 629, 10.1016/j.cell.2011.09.025 · DOI · Paper page
  69. Qiu, 2012, The aryl hydrocarbon receptor regulates gut immunity through modulation of innate lymphoid cells, Immunity, 36, 92, 10.1016/j.immuni.2011.11.011 · DOI · Paper page
  70. Stockinger, 2011, External influences on the immune system via activation of the aryl hydrocarbon receptor, Semin. Immunol., 23, 99, 10.1016/j.smim.2011.01.008 · DOI
  71. Gronke, 2019, Interleukin-22 protects intestinal stem cells against genotoxic stress, Nature, 566, 249, 10.1038/s41586-019-0899-7 · DOI · Paper page
  72. Hanash, 2012, Interleukin-22 protects intestinal stem cells from immune-mediated tissue damage and regulates sensitivity to graft versus host disease, Immunity, 37, 339, 10.1016/j.immuni.2012.05.028 · DOI · Paper page
  73. Lindemans, 2015, Interleukin-22 promotes intestinal-stem-cell-mediated epithelial regeneration, Nature, 528, 560, 10.1038/nature16460 · DOI · Paper page
  74. Caulfield, 2004, Undernutrition as an underlying cause of child deaths associated with diarrhea, pneumonia, malaria, and measles, Am. J. Clin. Nutr., 80, 193, 10.1093/ajcn/80.1.193 · DOI · Paper page
  75. Hall, 2011, The role of retinoic acid in tolerance and immunity, Immunity, 35, 13, 10.1016/j.immuni.2011.07.002 · DOI · Paper page
  76. van de Pavert, 2009, Chemokine CXCL13 is essential for lymph node initiation and is induced by retinoic acid and neuronal stimulation, Nat. Immunol., 10, 1193, 10.1038/ni.1789 · DOI · Paper page
  77. Beijer, 2014, Vitamin A and dendritic cell differentiation, Immunology, 142, 39, 10.1111/imm.12228 · DOI
  78. Grizotte-Lake, 2018, Commensals suppress intestinal epithelial cell retinoic acid synthesis to regulate interleukin-22 activity and prevent microbial dysbiosis, 1103
  79. Klebanoff, 2013, Retinoic acid controls the homeostasis of pre-cDC-derived splenic and intestinal dendritic cells, J. Exp. Med., 210, 1961, 10.1084/jem.20122508 · DOI
  80. Iwata, 2004, Retinoic acid imprints gut-homing specificity on T cells, Immunity, 21, 527, 10.1016/j.immuni.2004.08.011 · DOI · Paper page
  81. Mora, 2006, Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells, Science, 314, 1157, 10.1126/science.1132742 · DOI · Paper page
  82. Suzuki, 2010, The sensing of environmental stimuli by follicular dendritic cells promotes immunoglobulin A generation in the gut, Immunity, 33, 71, 10.1016/j.immuni.2010.07.003 · DOI
  83. Hall, 2011, Essential role for retinoic acid in the promotion of CD4(+) T cell effector responses via retinoic acid receptor alpha, Immunity, 34, 435, 10.1016/j.immuni.2011.03.003 · DOI · Paper page
  84. Sun, 2007, Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid, J. Exp. Med., 204, 1775, 10.1084/jem.20070602 · DOI · Paper page
  85. Coombes, 2007, A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism, 1757
  86. Mucida, 2009, Retinoic acid can directly promote TGF-beta-mediated Foxp3(+) Treg cell conversion of naive T cells, Immunity, 30, 471, 10.1016/j.immuni.2009.03.008 · DOI
  87. Wessells, 2012, Estimating the global prevalence of zinc deficiency: results based on zinc availability in national food supplies and the prevalence of stunting, PLoS One, 7, 10.1371/journal.pone.0050568 · DOI · Paper page
  88. Dardenne, 2002, Zinc and immune function, Eur. J. Clin. Nutr., 56, S20, 10.1038/sj.ejcn.1601479 · DOI
  89. Wong, 2007, Genome-level expression profiles in pediatric septic shock indicate a role for altered zinc homeostasis in poor outcome, Physiol. Genomics, 30, 146, 10.1152/physiolgenomics.00024.2007 · DOI
  90. Hassan, 2016, Impact of iron deficiency anemia on the function of the immune system in children, Medicine (Baltimore), 95, 10.1097/MD.0000000000005395 · DOI
  91. Das, 2014, Impact of iron deficiency anemia on cell-mediated and humoral immunity in children: a case control study, J. Nat. Sci. Biol. Med., 5, 158, 10.4103/0976-9668.127317 · DOI
  92. Moretti, 2015, Oral iron supplements increase hepcidin and decrease iron absorption from daily or twice-daily doses in iron-depleted young women, Blood, 126, 1981, 10.1182/blood-2015-05-642223 · DOI · Paper page
  93. Ganz, 2006, Hepcidin--a peptide hormone at the interface of innate immunity and iron metabolism, Curr. Top. Microbiol. Immunol., 306, 183
  94. La Rosa, 2014, Patterned progression of bacterial populations in the premature infant gut. [Published erratum appears in 2014 Proc. Natl. Acad. Sci. USA 111: 17336.], Proc. Natl. Acad. Sci. USA, 111, 12522, 10.1073/pnas.1409497111 · DOI · Paper page
  95. Koenig, 2011, Succession of microbial consortia in the developing infant gut microbiome, Proc. Natl. Acad. Sci. USA, 108, 4578, 10.1073/pnas.1000081107 · DOI · Paper page
  96. Subramanian, 2015, Cultivating healthy growth and nutrition through the gut microbiota, Cell, 161, 36, 10.1016/j.cell.2015.03.013 · DOI
  97. Robertson, 2019, The human microbiome and child growth - first 1000 days and beyond, Trends Microbiol., 27, 131, 10.1016/j.tim.2018.09.008 · DOI · Paper page
  98. Borelli, 2009, Protein-energy malnutrition halts hemopoietic progenitor cells in the G0/G1 cell cycle stage, thereby altering cell production rates, Braz. J. Med. Biol. Res., 42, 523, 10.1590/S0100-879X2009000600008 · DOI
  99. Conzen, 1988, Defective antigen presentation in chronically protein-deprived mice, Immunology, 63, 683
  100. Taylor, 2013, Protein energy malnutrition decreases immunity and increases susceptibility to influenza infection in mice, J. Infect. Dis., 207, 501, 10.1093/infdis/jis527 · DOI
  101. Schaible, 2007, Malnutrition and infection: complex mechanisms and global impacts, PLoS Med., 4, 10.1371/journal.pmed.0040115 · DOI · Paper page
  102. Kolčić, 2012, Double burden of malnutrition: a silent driver of double burden of disease in low- and middle-income countries, J. Glob. Health, 2, 10.7189/jogh.02.020303 · DOI
  103. Collins, 2019, The bone marrow protects and optimizes immunological memory during dietary restriction, 1088
  104. Jordan, 2019, Dietary intake regulates the circulating inflammatory monocyte pool, 1102
  105. Korpe, 2012, Environmental enteropathy: critical implications of a poorly understood condition, Trends Mol. Med., 18, 328, 10.1016/j.molmed.2012.04.007 · DOI · Paper page
  106. Keusch, 2014, Environmental enteric dysfunction: pathogenesis, diagnosis, and clinical consequences, Clin. Infect. Dis., 59, S207, 10.1093/cid/ciu485 · DOI · Paper page
  107. Crane, 2015, Environmental enteric dysfunction: an overview, Food Nutr. Bull., 36, S76, 10.1177/15648265150361S113 · DOI
  108. Petri, 2014, Environmental enteropathy and malnutrition: do we know enough to intervene?, BMC Med., 12, 187, 10.1186/s12916-014-0187-1 · DOI
  109. Naylor, 2015, Environmental enteropathy, oral vaccine failure and growth faltering in infants in Bangladesh, EBioMedicine, 2, 1759, 10.1016/j.ebiom.2015.09.036 · DOI · Paper page
  110. Johnson, 2012, Comparison of immune responses to the O-specific polysaccharide and lipopolysaccharide of Vibrio cholerae O1 in Bangladeshi adult patients with cholera, Clin. Vaccine Immunol., 19, 1712, 10.1128/CVI.00321-12 · DOI
  111. Grassly, 2009, Mucosal immunity after vaccination with monovalent and trivalent oral poliovirus vaccine in India, J. Infect. Dis., 200, 794, 10.1086/605330 · DOI
  112. Santos, 2005, Global distribution of rotavirus serotypes/genotypes and its implication for the development and implementation of an effective rotavirus vaccine, Rev. Med. Virol., 15, 29, 10.1002/rmv.448 · DOI · Paper page
  113. Katz, 2014, Can we say what diet is best for health?, Annu. Rev. Public Health, 35, 83, 10.1146/annurev-publhealth-032013-182351 · DOI · Paper page
  114. Zeevi, 2015, Personalized nutrition by prediction of glycemic responses, Cell, 163, 1079, 10.1016/j.cell.2015.11.001 · DOI · Paper page
  115. Wang, 2018, Glucose metabolism mediates disease tolerance in cerebral malaria, Proc. Natl. Acad. Sci. USA, 115, 11042, 10.1073/pnas.1806376115 · DOI
  116. Wang, 2016, Opposing effects of fasting metabolism on tissue tolerance in bacterial and viral inflammation, 1512

Cited by

See all 46

Metadata

Authors
Burr, A. H. P., Bhattacharjee, A., & Hand, T. W.
Affiliations
Richard King Mellon Institute for Pediatric Research, Department of Pediatrics, University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh, University of Pittsburgh , Pittsburgh, PA 15224
ORCID
Hand, Timothy W
Venue
The Journal of Immunology
Publisher
Oxford University Press (OUP)
Published
2020-09
Volume
205
Issue
6
Pages
1479-1487
ISSN
  • 0022-1767
  • 1550-6606
DOI
10.4049/jimmunol.2000419
Cited by
46
References
34
Language
en
Licence
academic.oup.com/pages/standard-publication-reuse-rights (vor)
Funders
  • National Institutes of Health, Office of Extramural Research (R21AI142051, T32AI089443)
  • Kenneth Rainin Foundation

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.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.