The DOI matches its Crossref record; 48 of the 49 references it cites were found in a registry or an index.
The Gut Microbiota Regulates Intestinal CD4 T Cells Expressing RORγt and Controls Metabolic Disease
Open accessAbstract
A high-fat diet (HFD) induces metabolic disease and low-grade metabolic inflammation in response to changes in the intestinal microbiota through as-yet-unknown mechanisms. Here, we show that a HFD-derived ileum microbiota is responsible for a decrease in Th17 cells of the lamina propria in axenic colonized mice. The HFD also changed the expression profiles of intestinal antigen-presenting cells and their ability to generate Th17 cells in vitro. Consistent with these data, the metabolic phenotype was mimicked in RORγt-deficient mice, which lack IL17 and IL22 function, and in the adoptive transfer experiment of T cells from RORγt-deficient mice into Rag1-deficient mice. We conclude that the microbiota of the ileum regulates Th17 cell homeostasis in the small intestine and determines the outcome of metabolic disease.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Insulin resistance that is induced through a high-fat diet is associated with reduced levels of T helper 17 (TH17) cells that are positive for IL-17 and retinoic acid receptor-related orphan receptor γt (RORγt)112.”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [112]
Citations
Cites
An obesity-associated gut microbiome with increased capacity for energy harvest
Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444
Obesity is associated with macrophage accumulation in adipose tissue
Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041
Inflammation and metabolic disorders
Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199
The gut microbiota as an environmental factor that regulates fat storage
Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245
Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145
Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819
Self-citationInduction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554
Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species
Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752
The gut microbiota--masters of host development and physiology
Sommer, F., & Bäckhed, F. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro2974 · Cited by 3,681
Commensal Host-Bacterial Relationships in the Gut
Hooper, L. V., & Gordon, J. I. (2001) · Science · doi:10.1126/science.1058709 · Cited by 2,362
Cited by
Sorted by citations
Diet–microbiota interactions as moderators of human metabolism
Sonnenburg, J. L., & Bäckhed, F. (2016) · Nature · doi:10.1038/nature18846 · Cited by 2,257
Impact of the gut microbiota on inflammation, obesity, and metabolic disease
Boulangé, C. L., Neves, A. L., Chilloux, J., Nicholson, J. K., & Dumas, M.-E. (2016) · Genome Medicine · doi:10.1186/s13073-016-0303-2 · Cited by 1,438
The intestinal microbiota fuelling metabolic inflammation
Tilg, H., Zmora, N., Adolph, T. E., & Elinav, E. (2020) · Nature Reviews Immunology · doi:10.1038/s41577-019-0198-4 · Cited by 1,089
High-Fat, Western-Style Diet, Systemic Inflammation, and Gut Microbiota: A Narrative Review
Malesza, I. J., Malesza, M., Walkowiak, J., Mussin, N. M., Walkowiak, D., Aringazina, R. A., Bartkowiak-Wieczorek, J., & Mądry, E. (2021) · Cells · doi:10.3390/cells10113164 · Cited by 847
GPCR-Mediated Signaling of Metabolites
Husted, A. S., Trauelsen, M., Rudenko, O., Hjorth, S. A., & Schwartz, T. W. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.03.008 · Cited by 602
The Treg/Th17 Axis: A Dynamic Balance Regulated by the Gut Microbiome
Omenetti, S., & Pizarro, T. T. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00639 · Cited by 545
He, B., Nohara, K., Park, N., Park, Y.-S., Guillory, B., Zhao, Z., Garcia, J. M., Koike, N., Lee, C. C., Takahashi, J. S., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.03.007 · Cited by 511
Obesity and diabetes as high‐risk factors for severe coronavirus disease 2019 ( Covid ‐19)
Zhou, Y., Chi, J., Lv, W., & Wang, Y. (2020) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.3377 · Cited by 522
Obesity, Inflammation, and Immune System in Osteoarthritis
Nedunchezhiyan, U., Varughese, I., Sun, A. R., Wu, X., Crawford, R., & Prasadam, I. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.907750 · Cited by 507
The Intestinal Immune System in Obesity and Insulin Resistance
Winer, D. A., Luck, H., Tsai, S. J., & Winer, S. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.01.003 · Cited by 493
Role of the Gut Microbiome in the Pathogenesis of Obesity and Obesity-Related Metabolic Dysfunction
Bouter, K. E. C., van Raalte, D. H., Groen, A. K., & Nieuwdorp, M. (2017) · Gastroenterology · doi:10.1053/j.gastro.2016.12.048 · Cited by 443
Role of the gut microbiota in host appetite control: bacterial growth to animal feeding behaviour
Fetissov, S. O. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2016.150 · Cited by 403
The dichotomous nature of T helper 17 cells
Stockinger, B., & Omenetti, S. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.50 · Cited by 419
Lipocalin-2: A Master Mediator of Intestinal and Metabolic Inflammation
Moschen, A. R., Adolph, T. E., Gerner, R. R., Wieser, V., & Tilg, H. (2017) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2017.01.003 · Cited by 359
Diabetes, infection risk and COVID-19
Erener, S. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101044 · Cited by 367
Kawano, Y., Edwards, M., Huang, Y., Bilate, A. M., Araujo, L. P., Tanoue, T., Atarashi, K., Ladinsky, M. S., Reiner, S. L., Wang, H. H., et al. (2022) · Cell · doi:10.1016/j.cell.2022.08.005 · Cited by 349
Gut Microbiota: An Important Player in Type 2 Diabetes Mellitus
Zhou, Z., Sun, B., Yu, D., & Zhu, C. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.834485 · Cited by 350
Kern, L., Mittenbühler, M., Vesting, A., Ostermann, A., Wunderlich, C., & Wunderlich, F. (2018) · Cancers · doi:10.3390/cancers11010024 · Cited by 331
Tissue Immune Cells Fuel Obesity-Associated Inflammation in Adipose Tissue and Beyond
Liu, R., & Nikolajczyk, B. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01587 · Cited by 318
Genetic deficiency of indoleamine 2,3-dioxygenase promotes gut microbiota-mediated metabolic health
Laurans, L., Venteclef, N., Haddad, Y., Chajadine, M., Alzaïd, F., Metghalchi, S., Sovran, B., Denis, R., Dairou, J., Cardellini, M., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0060-4 · Cited by 315
Self-citationGrasset, E., Puel, A., Charpentier, J., Collet, X., Christensen, J. E., Tercé, F., & Burcelin, R. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.013 · Cited by 284
Self-citationThe gut microbiome in Alzheimer’s disease: what we know and what remains to be explored
Chandra, S., Sisodia, S. S., & Vassar, R. J. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00595-7 · Cited by 278
Gut Microbial Dysbiosis in the Pathogenesis of Gastrointestinal Dysmotility and Metabolic Disorders
Singh, R., Zogg, H., Wei, L., Bartlett, A., Ghoshal, U. C., Rajender, S., & Ro, S. (2020) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm20149 · Cited by 274
The Alterations in and the Role of the Th17/Treg Balance in Metabolic Diseases
Zhang, S., Gang, X., Yang, S., Cui, M., Sun, L., Li, Z., & Wang, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.678355 · Cited by 263
Cytotoxic and regulatory roles of mucosal-associated invariant T cells in type 1 diabetes
Rouxel, O., silva, J. D., Beaudoin, L., Nel, I., Tard, C., Cagninacci, L., Kiaf, B., Oshima, M., Diedisheim, M., Salou, M., et al. (2017) · Nature Immunology · doi:10.1038/ni.3854 · Cited by 260
Linking the Microbiota, Chronic Disease, and the Immune System
Hand, T. W., Vujkovic-Cvijin, I., Ridaura, V. K., & Belkaid, Y. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.08.003 · Cited by 247
The role of T cells in age-related diseases
Carrasco, E., Heras, M. M. G. D. L., Gabandé‐Rodríguez, E., Desdín-Micó, G., Aranda, J. F., & Mittelbrunn, M. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00557-4 · Cited by 250
Lelouvier, B., Servant, F., Païssé, S., Brunet, A., Benyahya, S., Serino, M., Valle, C., Ortiz, M. R., Puig, J., Courtney, M., et al. (2016) · Hepatology · doi:10.1002/hep.28829 · Cited by 242
Self-citationRole of T Lymphocytes in Type 2 Diabetes and Diabetes-Associated Inflammation
Xia, C. Q., Rao, X., & Zhong, J. (2017) · Journal of Diabetes Research · doi:10.1155/2017/6494795 · Cited by 240
Gut Microbiota–Derived Short-Chain Fatty Acids Promote Prostate Cancer Growth via IGF1 Signaling
Matsushita, M., Fujita, K., Hayashi, T., Kayama, H., Motooka, D., Hase, H., Jingushi, K., Yamamichi, G., Yumiba, S., Tomiyama, E., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-4090 · Cited by 212
Li, X., Watanabe, K., & Kimura, I. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01882 · Cited by 216
Kawano, Y., Nakae, J., Watanabe, N., Kikuchi, T., Tateya, S., Tamori, Y., Kaneko, M., Abe, T., Onodera, M., & Itoh, H. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.07.009 · Cited by 207
Gut-associated IgA+ immune cells regulate obesity-related insulin resistance
Luck, H., Khan, S. M., Kim, J. H., Copeland, J. K., Revelo, X. S., Tsai, S. J., Chakraborty, M., Cheng, K., Chan, Y. T., Nøhr, M. K., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11370-y · Cited by 210
Microbiota in T-cell homeostasis and inflammatory diseases
Lee, N., & Kim, W. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.36 · Cited by 208
Gut microbiota and immune crosstalk in metabolic disease
Burcelin, R. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.05.016 · Cited by 195
Self-citationMancini, A., Bruno, C., Vergani, E., d’Abate, C., Giacchi, E., & Silvestrini, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041667 · Cited by 194
Regionalized Development and Maintenance of the Intestinal Adaptive Immune Landscape
Agace, W. W., & McCoy, K. D. (2017) · Immunity · doi:10.1016/j.immuni.2017.04.004 · Cited by 194
The role of diet and intestinal microbiota in the development of metabolic syndrome
Santos-Marcos, J. A., Pérez‐Jiménez, F., & Camargo, A. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.03.017 · Cited by 188
Stenman, L. K., Lehtinen, M. J., Meland, N., Christensen, J. E., Yeung, N., Saarinen, M. T., Courtney, M., Burcelin, R., Lähdeaho, M.-L., Linros, J., et al. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.10.036 · Cited by 177
Self-citationBian, Y., Lei, J., Zhong, J., Wang, B., Wan, Y., Li, J., Liao, C., He, Y., Liu, Z., Ito, K., et al. (2021) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2021.108840 · Cited by 175
Toubal, A., Kiaf, B., Beaudoin, L., Cagninacci, L., Rhimi, M., Fruchet, B., da Silva, J., Corbett, A. J., Simoni, Y., Lantz, O., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17307-0 · Cited by 165
Alteration in the Gut Microbiota Provokes Susceptibility to Tuberculosis
Khan, N., Vidyarthi, A., Nadeem, S., Negi, S., Nair, G. R., & Agrewala, J. N. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00529 · Cited by 163
Adipose Tissue-Resident Immune Cells in Obesity and Type 2 Diabetes
Lü, J., Zhao, J., Meng, H., & Zhang, X. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01173 · Cited by 164
Murakami, M., Tognini, P., Liu, Y., Eckel‐Mahan, K. L., Baldi, P., & Sassone‐Corsi, P. (2016) · EMBO Reports · doi:10.15252/embr.201642463 · Cited by 161
Bacteroides uniformis combined with fiber amplifies metabolic and immune benefits in obese mice
López‐Almela, I., Romaní‐Pérez, M., Bullich‐Vilarrubias, C., Benítez‐Páez, A., del Pulgar, E. M. G., Francés, R., Liebisch, G., & Sanz, Y. (2021) · Gut Microbes · doi:10.1080/19490976.2020.1865706 · Cited by 157
Emerging concepts in intestinal immune control of obesity-related metabolic disease
Khan, S. M., Luck, H., Winer, S., & Winer, D. A. (2021) · Nature Communications · doi:10.1038/s41467-021-22727-7 · Cited by 161
Intestinal microbiota and the immune system in metabolic diseases
Sittipo, P., Lobionda, S., Lee, Y. K., & Maynard, C. L. (2018) · The Journal of Microbiology · doi:10.1007/s12275-018-7548-y · Cited by 150
Calvo, S. S.-C., Bharath, L. P., Pugh, G. H., SantaCruz-Calvo, L., Lenin, R. R., Lutshumba, J., Liu, R., Bachstetter, A. D., Zhu, B., & Nikolajczyk, B. S. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00575-1 · Cited by 149
Rahim, M. B. H. A., Chilloux, J., Martínez-Gili, L., Neves, A. L., Myridakis, A., Gooderham, N. J., & Dumas, M. (2019) · Acta Diabetologica · doi:10.1007/s00592-019-01312-x · Cited by 127
Gestational diabetes is associated with changes in placental microbiota and microbiome
Bassols, J., Sérino, M., Carreras‐Badosa, G., Burcelin, R., Blasco‐Baqué, V., López‐Bermejo, A., & Fernández‐Real, J. M. (2016) · Pediatric Research · doi:10.1038/pr.2016.155 · Cited by 123
Self-citationHigh fat diet drives obesity regardless the composition of gut microbiota in mice
Rabot, S., Membrez, M., Blancher, F., Berger, B. W., Moine, D., Krause, L., Bibiloni, R., Bruneau, A., Gérard, P., Siddharth, J., et al. (2016) · Scientific Reports · doi:10.1038/srep32484 · Cited by 131
Diet, microbiota, and the mucus layer: The guardians of our health
Suriano, F., Nyström, E. E. L., Sergi, D., & Gustafsson, J. K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.953196 · Cited by 126
Berberine Attenuates Intestinal Mucosal Barrier Dysfunction in Type 2 Diabetic Rats
Gong, J., Hu, M., Huang, Z., Fang, K., Wang, D., Chen, Q., Li, J., Yang, D., Zou, X. G., Xu, L., et al. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00042 · Cited by 116
Gut-Specific Delivery of T-Helper 17 Cells Reduces Obesity and Insulin Resistance in Mice
Hong, C., Park, A., Yang, B., Yun, C. H., Kwak, M.-J., Lee, G.-W., Kim, J. H., Jang, M. S., Lee, E., Jeun, E.-J., et al. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.02.016 · Cited by 119
The Gut Microbiome as Therapeutic Target in Central Nervous System Diseases: Implications for Stroke
Winek, K., Dirnagl, U., & Meisel, A. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0475-x · Cited by 108
Malaisé, Y., Menard, S., Cartier, C., Gaultier, E., Lasserre, F., Lencina, C., Harkat, C., Geoffre, N., Lakhal, L., Castan, I., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15196-w · Cited by 107
T Cell Populations and Functions Are Altered in Human Obesity and Type 2 Diabetes
Touch, S., Clément, K., & André, S. (2017) · Current Diabetes Reports · doi:10.1007/s11892-017-0900-5 · Cited by 109
Palmitic acid damages gut epithelium integrity and initiates inflammatory cytokine production
Ghezzal, S., Postal, B. G., Quévrain, E., Brot, L., Seksik, P., Leturque, A., Thenet, S., & Carrière, V. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.158530 · Cited by 106
Th17 and Treg lymphocytes in obesity and Type 2 diabetic patients
Wang, M., Chen, F., Wang, J., Zeng, Z., Yang, Q., & Shao, S. (2018) · Clinical Immunology · doi:10.1016/j.clim.2018.09.005 · Cited by 102
Yun, Y., Kim, H.-N., Lee, E., Ryu, S., Chang, Y., Shin, H. C., Kim, H., Kim, T. H., Yoo, K., & Kim, H. Y. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213692 · Cited by 97
Microbiota and Diabetes Mellitus: Role of Lipid Mediators
Salazar, J. J., Angarita, L., Morillo, V., Navarro, C., Martínez, M. S., Chacín, M., Torres, W., Rajotia, A., Rojas, M., Cano, C., et al. (2020) · Nutrients · doi:10.3390/nu12103039 · Cited by 97
Silva, D., Viana, S., Carvalho, E., Reis, F., & Matafome, P. N. (2023) · Internal and Emergency Medicine · doi:10.1007/s11739-023-03262-3 · Cited by 103
Lipopolysaccharides: structure, function and bacterial identification
Caroff, M., & Novikov, A. (2020) · OCL · doi:10.1051/ocl/2020025 · Cited by 93
Mitochondrial function in intestinal epithelium homeostasis and modulation in diet-induced obesity
Guerbette, T., Boudry, G., & Lan, A. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101546 · Cited by 100
Qiu, X., Macchietto, M. G., Liu, X., Lu, Y., Ma, Y., Guo, H., Saqui–Salces, M., Bernlohr, D., Chen, C., Shen, S., et al. (2020) · International Journal of Obesity · doi:10.1038/s41366-020-00712-2 · Cited by 90
Guo, X., Tang, R., Yang, S., Lu, Y., Luo, J., & Liu, Z. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02651 · Cited by 89
Nutrition Regulates Innate Immunity in Health and Disease
Nobs, S. P., Zmora, N., & Elinav, E. (2020) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-120919-094440 · Cited by 93
Immunologic impact of the intestine in metabolic disease
Winer, D. A., Winer, S., Dranse, H. J., & Lam, T. K. T. (2017) · Journal of Clinical Investigation · doi:10.1172/jci88879 · Cited by 95
The gut microbiota mediates protective immunity against tuberculosis via modulation of lncRNA
Yang, F., Yang, Y., Chen, L., Zhang, Z., Liu, L., Zhang, C., Mai, Q., Chen, Z., Chen, Z., Lin, T., et al. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2029997 · Cited by 84
McPhee, J. B., & Schertzer, J. D. (2015) · Clinical Science · doi:10.1042/cs20150431 · Cited by 86
The intestinal immune system and gut barrier function in obesity and ageing
Shemtov, S. J., Emani, R., Bielska, O., Covarrubias, A. J., Verdin, E. M., Andersen, J. K., & Winer, D. A. (2022) · FEBS Journal · doi:10.1111/febs.16558 · Cited by 86
Crosstalk between γδ T cells and the microbiota
Papotto, P. H., Yılmaz, B., & Silva‐Santos, B. (2021) · Nature Microbiology · doi:10.1038/s41564-021-00948-2 · Cited by 83
The Role of Leukocytes in Diabetic Cardiomyopathy
Bajpai, A., & Tilley, D. G. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01547 · Cited by 80
Trindade, B. C., Ceglia, S., Berthelette, A., Raso, F., Howley, K., Muppidi, J. R., & Reboldi, A. (2021) · Immunity · doi:10.1016/j.immuni.2021.09.004 · Cited by 82
Stenman, L. K., Burcelin, R., & Lahtinen, S. J. (2015) · Beneficial Microbes · doi:10.3920/bm2015.0069 · Cited by 79
Self-citationNeto, H. A. P., Ausina, P., Gomez, L. S., Leandro, J. G. B., Zancan, P., & Sola‐Penna, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01478 · Cited by 81
Holdemanella biformis improves glucose tolerance and regulates GLP‐1 signaling in obese mice
Romaní‐Pérez, M., López‐Almela, I., Bullich‐Vilarrubias, C., Rueda‐Ruzafa, L., del Pulgar, E. M. G., Benítez‐Páez, A., Liebisch, G., Lamas, J. A., & Sanz, Y. (2021) · The FASEB Journal · doi:10.1096/fj.202100126r · Cited by 79
Gut microbiota and associated metabolites: key players in high-fat diet-induced chronic diseases
Du, W., Zou, Z., Ye, B., & Zhou, Y. Q. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2494703 · Cited by 84
Pérez, M. M., Martins, L. M. S., Dias, M. S., Pereira, C. A., Leite, J. A., Gonçalves, E. C. S., de Almeida, P. Z., de Freitas, E. N., Tostes, R. C., Ramos, S. G., et al. (2018) · Immunology · doi:10.1111/imm.13028 · Cited by 77
Bifidobacterium animalis subsp. lactis 420 for Metabolic Health: Review of the Research
Uusitupa, H., Rasinkangas, P., Lehtinen, M. J., Mäkelä, S. M., Airaksinen, K., Anglenius, H., Ouwehand, A. C., & Maukonen, J. (2020) · Nutrients · doi:10.3390/nu12040892 · Cited by 78
Riedel, S., Pheiffer, C., Johnson, R., Louw, J., & Muller, C. J. F. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.833544 · Cited by 78
Qian, X., Si, Q., Lin, G., Zhu, M., Lu, J., Zhang, H., Wang, G., & Chen, W. (2022) · Nutrients · doi:10.3390/nu14122479 · Cited by 72
Metabolic regulation of the Th17/Treg balance in inflammatory bowel disease
Zhang, S., Zhong, R., Tang, S., Chen, L., & Zhang, H. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107184 · Cited by 76
Fabersani, E., Portune, K. J., Campillo, I., López‐Almela, I., la Paz, S. M., Romaní‐Pérez, M., Benítez‐Páez, A., & Sanz, Y. (2021) · Scientific Reports · doi:10.1038/s41598-021-90888-y · Cited by 73
The Role of T Cells in Obesity-Associated Inflammation and Metabolic Disease
Park, C., & Shastri, N. (2022) · Immune Network · doi:10.4110/in.2022.22.e13 · Cited by 76
Probiotic B420 and prebiotic polydextrose improve efficacy of antidiabetic drugs in mice
Stenman, L. K., Waget, A., Garret, C., Briand, F., Burcelin, R., Sulpice, T., & Lahtinen, S. J. (2015) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-015-0075-7 · Cited by 68
Self-citationLin, Y., Luck, H., Khan, S. M., Schneeberger, P. H. H., Tsai, S. J., Clemente‐Casares, X., Lei, H., Leu, Y., Chan, Y. T., Chen, H., et al. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0340-1 · Cited by 73
Natural Polyphenols: A Potential Therapeutic Approach to Hypoglycemia
Zhao, C., Wan, X., Zhou, S. D., & Cao, H. (2020) · eFood · doi:10.2991/efood.k.200302.001 · Cited by 66
Zhu, G., Ma, F., Wang, G., Wang, Y., Zhao, J., Zhang, H., & Chen, W. (2018) · Food & Function · doi:10.1039/c8fo00100f · Cited by 63
The Functional Stability of FOXP3 and RORγt in Treg and Th17 and Their Therapeutic Applications
Ren, J., & Li, B. (2016) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2016.10.002 · Cited by 66
Ursolic Acid Improves Intestinal Damage and Bacterial Dysbiosis in Liver Fibrosis Mice
Wan, S., Liu, C., Huang, C., Luo, F., & Zhu, X. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01321 · Cited by 60
Circadian Rhythms in Adipose Tissue Physiology
Kiehn, J., Tsang, A. H. K., Heyde, I., Leinweber, B., Kolbe, I., Leliavski, A., & Oster, H. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160017 · Cited by 64
T helper 17 (Th17) cell responses to the gut microbiota in human diseases
Sun, C., Yang, N. Y., Zheng, Z., Liu, D., & Xu, Q. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114483 · Cited by 60
Wheat Consumption Aggravates Colitis in Mice via Amylase Trypsin Inhibitor–mediated Dysbiosis
Pickert, G., Wirtz, S. J., Matzner, J., Ashfaq–Khan, M., Heck, R., Rosigkeit, S., Thies, D., Surabattula, R., Ehmann, D., Wehkamp, J., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.03.064 · Cited by 60
Gut Microbiota and IL-17A: Physiological and Pathological Responses
Douzandeh-Mobarrez, B., & Kariminik, A. (2017) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-017-9329-z · Cited by 60
Pomié, C., Blasco‐Baqué, V., Klopp, P., Nicolas, S., Waget, A., Loubières, P., Azalbert, V., Puel, A., Lopez, F., Dray, C., et al. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.03.004 · Cited by 57
Self-citationCavallari, J. F., Denou, E., Foley, K. P., Khan, W. I., & Schertzer, J. D. (2016) · Gut Microbes · doi:10.1080/19490976.2015.1127481 · Cited by 55
Besnard, P., Christensen, J. E., Brignot, H., Bernard, A., Passilly‐Degrace, P., Nicklaus, S., de Barros, J.-P. P., Collet, X., Lelouvier, B., Servant, F., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-24619-1 · Cited by 55
Self-citationTransfer of dysbiotic gut microbiota has beneficial effects on host liver metabolism
Nicolas, S., Blasco‐Baqué, V., Fournel, A., Gilleron, J., Klopp, P., Waget, A., Ceppo, F., Marlin, A., Padmanabhan, R., Iacovoni, J. S., et al. (2017) · Molecular Systems Biology · doi:10.15252/msb.20167356 · Cited by 60
Self-citationHuang, J., Li, W., Liao, W., Hao, Q., Tang, D., Wang, D., Wang, Y., & Ge, G. (2020) · Food & Function · doi:10.1039/d0fo02152k · Cited by 51
Metadata
- Authors
- Garidou, L., Pomié, C., Klopp, P., Waget, A., Charpentier, J., Aloulou, M., Giry, A., Serino, M., Stenman, L., Lahtinen, S., Dray, C., Iacovoni, J. S., Courtney, M., Collet, X., Amar, J., Servant, F., Lelouvier, B., Valet, P., Eberl, G., Fazilleau, N., Douin-Echinard, V., Heymes, C., & Burcelin, R.
- Affiliations
- Université Toulouse III - Paul Sabatier (FR)
- Centre National de la Recherche Scientifique (FR)
- Inserm (FR)
- Institut Pasteur (FR)
- Corresponding author
- Garidou, Lucile
- Burcelin, Rémy
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2015-07
- Volume
- 22
- Issue
- 1
- Pages
- 100-112
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W1483529702
- Cited by
- 303
- References
- 49
- Citations by year
- 2026: 12 · 2025: 17 · 2024: 24 · 2023: 32 · 2022: 29 · 2021: 50 · 2020: 23 · 2019: 30 · 2018: 20 · 2017: 34 · 2016: 25 · 2015: 7
- FWCI
- 12.43
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- gut microbiota, RORγt, Th17 cells, high-fat diet, metabolic disorders, metabolic inflammation, lamina propria, antigen-presenting cells, IL-17, IL-22, adoptive T cell therapy, Rag1-deficient mice
- MeSH terms
- Gastrointestinal Microbiome, Animals, Cells, Cultured, Diabetes Mellitus, Type 2, Gene Expression Regulation, Ileum, Immunity, Male, Obesity, CD4-Positive T-Lymphocytes, CD4 Antigens, Gene Deletion, Interleukin-17, Mice, Nuclear Receptor Subfamily 1, Group F, Member 3, Th17 Cells, Diet, High-Fat
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