The DOI matches its Crossref record; 255 of the 258 references it cites were found in a registry or an index.
Role of the microbiota in immunity and inflammation.
Open accessAbstract
The microbiota plays a fundamental role on the induction, training, and function of the host immune system. In return, the immune system has largely evolved as a means to maintain the symbiotic relationship of the host with these highly diverse and evolving microbes. When operating optimally, this immune system-microbiota alliance allows the induction of protective responses to pathogens and the maintenance of regulatory pathways involved in the maintenance of tolerance to innocuous antigens. However, in high-income countries, overuse of antibiotics, changes in diet, and elimination of constitutive partners, such as nematodes, may have selected for a microbiota that lack the resilience and diversity required to establish balanced immune responses. This phenomenon is proposed to account for some of the dramatic rise in autoimmune and inflammatory disorders in parts of the world where our symbiotic relationship with the microbiota has been the most affected.
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.
Integrity signals
Registry
Cites
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.
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
“While the impact of most of these substances on human health is not entirely clear at this point, evidence suggests that they are potentially harmful, with possible carcinogenic, teratogenic, and mutagenic effects and reproductive developmental toxicity [66]; in addition, they may disrupt the normal functioning of gut microbiota [67] and the endocrine system [68].”
From Bottled Water: An Evidence-Based Overview of Economic Viability, Environmental Impact, and Social Equity (2023) · cites this paper as [67]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The microbiota in the stomach promotes gut health and immunological balance by suppressing inflammation (10).”
From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [10]
Experimental — accuracy not yet measuredIn the citing paper
“endogenous symbiont microorganisms, the so-called microbiota, can modulate gene expression, induce preferential food intake (Aydin, 2007), influence pH, redox balance and the ratio between pro-inflammatory and anti-inflammatory cytokines (Belkaid and Hand, 2014).”
From Bioactive Molecules Released in Food by Lactic Acid Bacteria: Encrypted Peptides and Biogenic Amines (2016) · cites this paper as Belkaid and Hand, 2014
In the citing paper
“The intestinal microbiota play a role in host physiology.1”
From Microbiota as Predictor of Mortality in Allogeneic Hematopoietic-Cell Transplantation (2020) · cites this paper as [1]
In the citing paper
“The gut microbial population plays a key role in training, functioning and stimulating the host immune system, with the final effect of developing tolerance towards beneficial microbiota and eliciting immune response against gut pathogens [76].”
From Gut Microbiota and Cancer: From Pathogenesis to Therapy (2019) · cites this paper as [76]
In the citing paper
“Several studies have reported an association of dysbiosis with chronic inflammation, which may in turn result in an association with bone diseases [129,132,215,216].”
From Bone diseases in patients with chronic liver disease (2019) · cites this paper as [215]
In the citing paper
“Variations in these early interactions appear to set the tone of the mucosal and systemic immune systems into childhood and even adult life (Belkaid and Hand, 2014).”
From Viral Infections, the Microbiome, and Probiotics (2021) · cites this paper as Belkaid and Hand, 2014
In the citing paper
“The gut microbiota play a critical role in the development of the intestinal architecture and mucosal immune system and are particularly important for regulation of the immune system in the gut [reviewed in [13, 14]].”
From The Gut Microbiota and Dysbiosis in Autism Spectrum Disorders (2018) · cites this paper as [13]
In the citing paper
“These mice experience immune dysfunction and are more susceptible to infections than mice kept in conventional facilities [13, 15].”
From The Gut Microbiota and Dysbiosis in Autism Spectrum Disorders (2018) · cites this paper as [13]
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
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
Human gut microbes associated with obesity
Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785
Human gut microbiome viewed across age and geography
Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815
A metagenome-wide association study of gut microbiota in type 2 diabetes
Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762
Takeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141126 · Cited by 6,143
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549
Diversity, stability and resilience of the human gut microbiota
Lozupone, C. A., Stombaugh, J. I., Gordon, J. I., Jansson, J. K., & Knight, R. (2012) · Nature · doi:10.1038/nature11550 · Cited by 5,533
Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration
Marshall, B., & Warren, J. R. (1984) · The Lancet · doi:10.1016/s0140-6736(84)91816-6 · Cited by 5,509
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838
Flagged first, then by citations
3 of the 258 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 201–300 of 1,029
Desired Turbulence? Gut-Lung Axis, Immunity, and Lung Cancer
Bingula, R., Filaire, M., Radosevic‐Robin, N., Bey, M., Berthon, J., Bernalier‐Donadille, A., Vasson, M., & Filaire, E. (2017) · Journal of Oncology · doi:10.1155/2017/5035371 · Cited by 279
Wang, H., Wang, N., Wang, B., Zhao, Q., Fang, H., Fu, C., Tang, C., Jiang, F., Zhou, Y., Chen, Y., et al. (2016) · Environmental Science & Technology · doi:10.1021/acs.est.5b05749 · Cited by 268
The liver–brain–gut neural arc maintains the Treg cell niche in the gut
Teratani, T., Mikami, Y., Nakamoto, N., Suzuki, T., Harada, Y., Okabayashi, K., Hagihara, Y., Taniki, N., Kohno, K., Shibata, S., et al. (2020) · Nature · doi:10.1038/s41586-020-2425-3 · Cited by 270
A Gut Commensal Bacterium Promotes Mosquito Permissiveness to Arboviruses
Wu, P., Sun, P., Nie, K., Zhu, Y., Shi, M., Xiao, C., Liu, H., Liu, Q., Zhao, T., Chen, X., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.11.004 · Cited by 270
Kamo, T., Akazawa, H., Suda, W., Saga-Kamo, A., Shimizu, Y., Yagi, H., Liu, Q., Nomura, S., Naito, A. T., Takeda, N., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174099 · Cited by 268
Paradoxical gastrointestinal effects of interleukin-17 blockers
Fauny, M., Moulin, D., D’Amico, F., Netter, P., Petitpain, N., Arnone, D., Jouzeau, J., Lœuille, D., & Peyrin‐Biroulet, L. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-217927 · Cited by 266
Araújo, J. R., Tomas, J., Brenner, C., & Sansonetti, P. J. (2017) · Biochimie · doi:10.1016/j.biochi.2017.05.019 · Cited by 271
Emerging Functions of Regulatory T Cells in Tissue Homeostasis
Sharma, A., & Rudra, D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00883 · Cited by 273
Gut microbiota of aquatic organisms: A key endpoint for ecotoxicological studies
Evariste, L., Barret, M., Mottier, A., Mouchet, F., Gauthier, L., & Pinelli, É. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.02.101 · Cited by 269
Human Gut Bacterial Metabolism Drives Th17 Activation and Colitis
Alexander, M., Ang, Q. Y., Nayak, R. R., Bustion, A. E., Sandy, M., Zhang, B., Upadhyay, V., Pollard, K. S., Lynch, S. V., & Turnbaugh, P. J. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2021.11.001 · Cited by 270
The lung microbiome regulates brain autoimmunity
Hosang, L., Canals, R. C., van der Flier, F. J., Hollensteiner, J., Daniel, R., Flügel, A., & Odoardi, F. (2022) · Nature · doi:10.1038/s41586-022-04427-4 · Cited by 263
Intratumoural microbiota: a new frontier in cancer development and therapy
Cao, Y., Xia, H., Tan, X., Shi, C., Ma, Y., Meng, D., Zhou, M., Lv, Z., Wang, S., & Jin, Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01693-0 · Cited by 269
Wu, J., Li, Q., & Fu, X. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.03.003 · Cited by 259
The Relationship Between Gut Microbiota and Inflammatory Diseases: The Role of Macrophages
Wang, J., Chen, W., & Wang, Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01065 · Cited by 269
Simpson, R. C., Shanahan, E. R., Batten, M., Reijers, I. L. M., Read, M., Silva, I. P., Versluis, J. M., Ribeiro, R., Angelatos, A. S., Tan, J., et al. (2022) · Nature Medicine · doi:10.1038/s41591-022-01965-2 · Cited by 256
Multisystem inflammatory syndrome in children and Kawasaki disease: a critical comparison
Sharma, C., Ganigara, M., Galeotti, C., Burns, J., Berganza, F. M., Hayes, D. A., Singh‐Grewal, D., Bharath, S., Sajjan, S., & Bayry, J. (2021) · Nature Reviews Rheumatology · doi:10.1038/s41584-021-00709-9 · Cited by 263
Santis, S. D., Galleggiante, V., Scandiffio, L., Liso, M., Sommella, E., Sobolewski, A., Spilotro, V., Pinto, A., Campiglia, P., Serino, G., et al. (2017) · Nutrients · doi:10.3390/nu9070706 · Cited by 252
Effect of nutrition on neurodegenerative diseases. A systematic review
Bianchi, V. E., Herrera, P. F., & Rizzi, L. (2019) · Nutritional Neuroscience · doi:10.1080/1028415x.2019.1681088 · Cited by 268
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
Two to Tango: Dialog between Immunity and Stem Cells in Health and Disease
Naik, S., Larsen, S. B., Cowley, C. J., & Fuchs, E. V. (2018) · Cell · doi:10.1016/j.cell.2018.08.071 · Cited by 246
Microbiome and pathogen interaction with the immune system
Kogut, M. H., Lee, A., & Santín, E. (2020) · Poultry Science · doi:10.1016/j.psj.2019.12.011 · Cited by 266
Evolution, human-microbe interactions, and life history plasticity
Rook, G., Bäckhed, F., Levin, B. R., McFall-Ngai, M. J., & McLean, A. R. (2017) · The Lancet · doi:10.1016/s0140-6736(17)30566-4 · Cited by 246
Microbiota-mediated inflammation and antimicrobial defense in the intestine
Caballero, S., & Pamer, E. G. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032713-120238 · Cited by 238
The Microbiome of the Prostate Tumor Microenvironment
Cavarretta, I. T. R., Ferrarese, R., Cazzaniga, W., Saita, D., Lucianò, R., Ceresola, E. R., Locatelli, I., Visconti, L. M., Lavorgna, G., Briganti, A., et al. (2017) · European Urology · doi:10.1016/j.eururo.2017.03.029 · Cited by 251
Inflammatory Bowel Diseases and Gut Microbiota
Haneishi, Y., Furuya, Y., Hasegawa, M., Picarelli, A., Rossi, M., & Miyamoto, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043817 · Cited by 263
Novel players in coeliac disease pathogenesis: role of the gut microbiota
Verdu, E. F., Galipeau, H. J., & Jabrì, B. (2015) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.90 · Cited by 251
The small intestine microbiota, nutritional modulation and relevance for health
El Aidy, S., van den Bogert, B., & Kleerebezem, M. (2015) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2014.09.005 · Cited by 244
Interactions Between the Gut Microbiota and the Host Innate Immune Response Against Pathogens
Cheng, H.-Y., Ning, M.-X., Chen, D.-K., & Ma, W.-T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00607 · Cited by 244
Growth Factor FGF2 Cooperates with Interleukin-17 to Repair Intestinal Epithelial Damage
Song, X., Dai, D., He, X., Zhu, S., Yao, Y., Gao, H., Wang, J., Qu, F., Qiu, J., Wang, H., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.06.024 · Cited by 249
Gut microbiota–brain axis in depression: the role of neuroinflammation
Carlessi, A. S., Borba, L. A., Zugno, A. I., Quevedo, J., & Réus, G. Z. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.14631 · Cited by 243
Biodiversity’s contributions to sustainable development
Blicharska, M., SMITHERS, R. J., Mikusiński, G., Rönnbäck, P., Harrison, P. A., Nilsson, M., & Sutherland, W. J. (2019) · Nature Sustainability · doi:10.1038/s41893-019-0417-9 · Cited by 258
Nawaz, A., Javaid, A. B., Irshad, S., Hoseinifar, S. H., & Xiong, H. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.03.004 · Cited by 248
Kim, J. E., & Kim, H. S. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8040444 · Cited by 249
Cantorna, M. T., Snyder, L. M., & Arora, J. (2019) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2019.1611734 · Cited by 244
Microbiome Dependent Regulation of Tregs and Th17 Cells in Mucosa
Pandiyan, P., Bhaskaran, N., Zou, M., Schneider, E., Jayaraman, S., & Huehn, J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00426 · Cited by 237
Oral–Gut Microbiome Axis in Gastrointestinal Disease and Cancer
Park, S.-Y., Hwang, B.-O., Lim, M., Ok, S.-H., Lee, S., Chun, K., Park, K.-K., Hu, Y., Chung, W., & Song, N. (2021) · Cancers · doi:10.3390/cancers13092124 · Cited by 247
Impact of Fecal Microbiota Transplantation on Obesity and Metabolic Syndrome—A Systematic Review
Zhang, Z., Mocanu, V., Cai, C., Dang, J. T., Slater, L., Deehan, E. C., Walter, J., & Madsen, K. L. (2019) · Nutrients · doi:10.3390/nu11102291 · Cited by 245
The Influence of Lung Microbiota on Lung Carcinogenesis, Immunity, and Immunotherapy
Ramírez-Labrada, A., Isla, D., Artal, A., Arias, M. A., Rezusta, A., Pardo, J., & Gálvez, E. M. (2020) · Trends in cancer · doi:10.1016/j.trecan.2019.12.007 · Cited by 236
Anti-inflammatory potential of Quercetin in COVID-19 treatment
Saeedi‐Boroujeni, A., & Mahmoudian‐Sani, M. (2021) · Journal of Inflammation · doi:10.1186/s12950-021-00268-6 · Cited by 240
Inulin fibre promotes microbiota-derived bile acids and type 2 inflammation
Arifuzzaman, M., Won, T. H., Li, T., Yano, H., Digumarthi, S., Heras, A. F., Zhang, W., Parkhurst, C. N., Kashyap, S., Jin, W., et al. (2022) · Nature · doi:10.1038/s41586-022-05380-y · Cited by 240
Staley, C. M., Kaiser, T., Beura, L. K., Hamilton, M. J., Weingarden, A. R., Bobr, A., Kang, J., Masopust, D., Sadowsky, M. J., & Khoruts, A. (2017) · Microbiome · doi:10.1186/s40168-017-0306-2 · Cited by 241
The dual role of short fatty acid chains in the pathogenesis of autoimmune disease models
Mizuno, M., Noto, D., Kaga, N., Chiba, A., & Miyake, S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173032 · Cited by 230
Effector Vγ9Vδ2 T cells dominate the human fetal γδ T-cell repertoire
Dimova, T., Brouwer, M., Gosselin, F., Tassignon, J., Léo, O., Donner, C., Marchant, A., & Vermijlen, D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412058112 · Cited by 241
Memory CD4+ T Cells in Immunity and Autoimmune Diseases
Raphael, I., Robinson, R. R., & Forsthuber, T. G. (2020) · Cells · doi:10.3390/cells9030531 · Cited by 241
Dysbiosis in chronic periodontitis: Key microbial players and interactions with the human host
Deng, Z.-L., Szafrański, S. P., Jarek, M., Bhuju, S., & Wagner‐Döbler, I. (2017) · Scientific Reports · doi:10.1038/s41598-017-03804-8 · Cited by 230
Martínez-López, M., Iborra, S., Conde-Garrosa, R., Mastrangelo, A., Danne, C., Mann, E. R., Reid, D. M., Gaboriau-Routhiau, V., Chaparro, M., Lorenzo, M. P., et al. (2019) · Immunity · doi:10.1016/j.immuni.2018.12.020 · Cited by 228
Host immunoglobulin G selectively identifies pathobionts in pediatric inflammatory bowel diseases
Armstrong, H., Alipour, M., Valcheva, R. S., Bording‐Jorgensen, M., Jovel, J., Zaidi, D., Shah, P., Lou, Y., Ebeling, C., Mason, A. L., et al. (2019) · Microbiome · doi:10.1186/s40168-018-0604-3 · Cited by 228
Is resolution the end of inflammation?
Feehan, K. T., & Gilroy, D. W. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.01.006 · Cited by 229
The intratumor mycobiome promotes lung cancer progression via myeloid-derived suppressor cells
Liu, N., Yi, C., Wei, L., Zhou, J., Jiang, T., Hu, C.-C., Wang, L., Wang, Y.-Y., Zou, Y., Zhao, Y.-K., et al. (2023) · Cancer Cell · doi:10.1016/j.ccell.2023.08.012 · Cited by 231
The Gut Microbiota and Dysbiosis in Autism Spectrum Disorders
Hughes, H. K., Rose, D., & Ashwood, P. (2018) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-018-0887-6 · Cited by 225
Deehan, E. C., Duar, R. M., Armet, A. M., Pérez-Muñoz, M. E., Jin, M., & Walter, J. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.bad-0019-2017 · Cited by 240
van der Lugt, B., van Beek, A. A., Aalvink, S., Meijer, B., Sovran, B., Vermeij, W. P., Brandt, R. M. C., de Vos, W. M., Savelkoul, H. F. J., Steegenga, W. T., et al. (2019) · Immunity & Ageing · doi:10.1186/s12979-019-0145-z · Cited by 217
Intestinal microbiome and fitness in kidney disease
Meijers, B. K. I., Evenepoel, P., & Anders, H. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0172-1 · Cited by 228
Making Sense of … the Microbiome in Psychiatry
Bastiaanssen, T. F. S., Cowan, C. S. M., Claesson, M. J., Dinan, T. G., & Cryan, J. F. (2018) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyy067 · Cited by 234
Intestinal lymphatic vasculature: structure, mechanisms and functions
Bernier‐Latmani, J., & Petrova, T. V. (2017) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.79 · Cited by 219
Circulating exosomes suppress the induction of regulatory T cells via let-7i in multiple sclerosis
Kimura, K., Hohjoh, H., Fukuoka, M., Sato, W., Oki, S., Tomi, C., Yamaguchi, H., Kondo, T., Takahashi, R., & Yamamura, T. (2017) · Nature Communications · doi:10.1038/s41467-017-02406-2 · Cited by 223
Reynolds, L. A., Finlay, B. B., & Maizels, R. M. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1501432 · Cited by 226
Blum, H. E. (2017) · Advances in Medical Sciences · doi:10.1016/j.advms.2017.04.005 · Cited by 246
Elison, E., Vigsnaes, L. K., Rindom Krogsgaard, L., Rasmussen, J., Sørensen, N., McConnell, B., Hennet, T., Sommer, M. O. A., & Bytzer, P. (2016) · British Journal of Nutrition · doi:10.1017/s0007114516003354 · Cited by 218
Gray, J. K., Oehrle, K., Worthen, G. S., Alenghat, T., Whitsett, J. A., & Deshmukh, H. S. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf9412 · Cited by 223
Selective Manipulation of the Gut Microbiota Improves Immune Status in Vertebrates
Montalban‐Arques, A., Schryver, P. D., Bossier, P., Gorkiewicz, G., Mulero, V., Gatlin, D. M., & Galindo‐Villegas, J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00512 · Cited by 224
Alterations of the Skin and Gut Microbiome in Psoriasis and Psoriatic Arthritis
Olejniczak‐Staruch, I., Ciążyńska, M. A., Sobolewska-Sztychny, D., Narbutt, J., Skibińska, M., & Lesiak, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083998 · Cited by 234
Gut microbiota, inflammation, and molecular signatures of host response to infection
Gou, W., Fu, Y., Yue, L., Chen, G., Cai, X., Shuai, M., Xu, F., Yi, X., Chen, H., Zhu, Y., et al. (2021) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2021.04.002 · Cited by 220
Kim, M., Galan, C., Hill, A. A., Wu, W.-J., Fehlner-Peach, H., Song, H. W., Schady, D., Bettini, M. L., Simpson, K. W., Longman, R. S., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.05.009 · Cited by 202
“Epidemiological studies suggest that increased antibiotic exposure is associated with an increased risk for developing inflammatory diseases including IBD, celiac disease, and allergy (Belkaid and Hand, 2014) and our data suggest that this increased pathology could be due to a loss of microbiota-driven anti-inflammato…”
Houston, S. A., Cerovic, V., Thomson, C. A., Brewer, J. M., Mowat, A. M., & Milling, S. W. F. (2015) · Mucosal Immunology · doi:10.1038/mi.2015.77 · Cited by 214
A prospective view of animal and human Fasciolosis
Cwiklinski, K., O’Neill, S. M., Donnelly, S., & Dalton, J. P. (2016) · Parasite Immunology · doi:10.1111/pim.12343 · Cited by 223
Chandan, K., Gupta, M., & Sarwat, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2019.03081 · Cited by 213
Dysregulation of ILC3s unleashes progression and immunotherapy resistance in colon cancer
Goc, J., Lv, M., Bessman, N. J., Flamar, A.-L., Sahota, S., Suzuki, H., Teng, F., Putzel, G., Eberl, G., Withers, D. R., et al. (2021) · Cell · doi:10.1016/j.cell.2021.07.029 · Cited by 214
Modulation of the gut microbiota by metformin improves metabolic profiles in aged obese mice
Lee, H., Lee, Y., Kim, J., An, J., Lee, S., Kong, H., Song, Y., Lee, C.-K., & Kim, K. (2018) · Gut Microbes · doi:10.1080/19490976.2017.1405209 · Cited by 203
Intestinal Barrier and Permeability in Health, Obesity and NAFLD
Portincasa, P., Bonfrate, L., Khalil, M., Angelis, M. D., Calabrese, F. M., D’Amato, M., Wang, D. Q. ‐., & Ciaula, A. D. (2021) · Biomedicines · doi:10.3390/biomedicines10010083 · Cited by 219
Impacts of microplastics on immunity
Yang, W., Jannatun, N., Zeng, Y., Liu, T., Zhang, G., Chen, C., & Li, Y. (2022) · Frontiers in Toxicology · doi:10.3389/ftox.2022.956885 · Cited by 222
One Health Relationships Between Human, Animal, and Environmental Microbiomes: A Mini-Review
Trinh, P., Zaneveld, J., Safranek, S. M., & Rabinowitz, P. M. (2018) · Frontiers in Public Health · doi:10.3389/fpubh.2018.00235 · Cited by 215
Dey, P. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.104367 · Cited by 216
Trained immunity: adaptation within innate immune mechanisms
Domínguez‐Andrés, J., dos Santos, J. C., Bekkering, S., Mulder, W. J. M., van der Meer, J. W. M., Riksen, N. P., Joosten, L. A. B., & Netea, M. G. (2022) · Physiological Reviews · doi:10.1152/physrev.00031.2021 · Cited by 227
Calcinotto, A., Brevi, A., Chesi, M., Ferrarese, R., Garcia Perez, L., Grioni, M., Kumar, S., Garbitt, V. M., Sharik, M. E., Henderson, K. J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07305-8 · Cited by 223
Regulation of the T Cell Response by CD39
Takenaka, M. C., Robson, S. C., & Quintana, F. J. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.04.009 · Cited by 211
Sasso, J. M., Ammar, R. M., Tenchov, R., Lemmel, S. A., Kelber, O., Grieswelle, M., & Zhou, Q. A. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00127 · Cited by 229
Kim, Y., Kim, G., Kim, S., Cho, B., Kim, S., Do, E., Bae, D., Kim, S., Kweon, M., Song, J. S., et al. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.06.010 · Cited by 221
Chidambaram, S. B., Essa, M. M., Rathipriya, A. G., Bishir, M., Ray, B., Mahalakshmi, A. M., Tousif, A. H., Sakharkar, M. K., Kashyap, R. S., Friedland, R. P., et al. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107988 · Cited by 204
Immune-based therapies for hepatocellular carcinoma
Pinato, D. J., Guerra, N., Fessas, P., Murphy, R., Mineo, T., Mauri, F. A., Mukherjee, S. K., Thursz, M. R., Wong, C. N., Sharma, R., et al. (2020) · Oncogene · doi:10.1038/s41388-020-1249-9 · Cited by 202
Holobionts as Units of Selection and a Model of Their Population Dynamics and Evolution
Roughgarden, J. E., Gilbert, S. F., ROSENBERG, E. B., Zilber‐Rosenberg, I., & Lloyd, E. A. (2017) · Biological Theory · doi:10.1007/s13752-017-0287-1 · Cited by 206
Cohen, L. J., Cho, J. H., Gevers, D., & Chu, H. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.03.017 · Cited by 209
Gut Bacteriophage: Current Understanding and Challenges
Sutton, T., & Hill, C. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00784 · Cited by 199
Tools for Analysis of the Microbiome
Galloway-Peña, J., & Hanson, B. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06091-y · Cited by 234
Anti-Inflammatory and Immunomodulatory Properties of Fermented Plant Foods
Shahbazi, R., Sharifzad, F., Bagheri, R., Alsadi, N., Yasavoli‐Sharahi, H., & Matar, C. (2021) · Nutrients · doi:10.3390/nu13051516 · Cited by 216
Zhang, Y., Chen, R., Zhang, D., Qi, S., & Liu, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114295 · Cited by 224
Links between the microbiome and bone
Hernandez, C. J., Guss, J. D., Luna, M., & Goldring, S. R. (2016) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2887 · Cited by 200
Veterinary antibiotics in food, drinking water, and the urine of preschool children in Hong Kong
Li, N., Ho, W., Ying, G., & Deng, W. (2017) · Environment International · doi:10.1016/j.envint.2017.08.014 · Cited by 204
Antioxidant Activity, Metabolism, and Bioavailability of Polyphenols in the Diet of Animals
Bešlo, D., Golubić, N., Rastija, V., Agić, D., Karnaš, M., Šubarić, D., & Lučić, B. (2023) · Antioxidants · doi:10.3390/antiox12061141 · Cited by 226
Participation of Short-Chain Fatty Acids and Their Receptors in Gut Inflammation and Colon Cancer
Carretta, M. D., Quiroga, J., López‐Muñoz, R., Hidalgo, M. A., & Burgos, R. A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.662739 · Cited by 209
How and why do T cells and their derived cytokines affect the injured and healthy brain?
Filiano, A. J., Gadani, S. P., & Kipnis, J. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.39 · Cited by 199
Martínez, I., Maldonado-Gomez, M. X., Gomes-Neto, J. C., Kittana, H., Ding, H., Schmaltz, R., Joglekar, P., Cardona, R. J., Marsteller, N. L., Kembel, S. W., et al. (2018) · eLife · doi:10.7554/elife.36521 · Cited by 199
Liu, S., Rezende, R. M., Moreira, T. G., Tankou, S. K., Cox, L. M., Wu, M., Song, A., Dhang, F. H., Wei, Z., Costamagna, G., et al. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.10.008 · Cited by 206
Regulating T-cell differentiation through the polyamine spermidine
Carriche, G. M., Almeida, L., Stüve, P., Velásquez, L. N., Dhillon-LaBrooy, A., Roy, U., Lindenberg, M., Strowig, T., Plaza‐Sirvent, C., Schmitz, I., et al. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.04.037 · Cited by 205
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
Endogenous retroviruses promote homeostatic and inflammatory responses to the microbiota
Lima-Junior, D. S., Krishnamurthy, S. R., Bouladoux, N. J., Collins, N., Han, S., Chen, Y. E., Constantinides, M. G., Link, V. M., Lim, A. I., Enamorado, M., et al. (2021) · Cell · doi:10.1016/j.cell.2021.05.020 · Cited by 204
Self-citationInnate Lymphoid Cells in Intestinal Homeostasis and Inflammatory Bowel Disease
Saéz, Á., Gómez-Bris, R., Herrero‐Fernández, B., Mingorance, C., Rius, C., & González, J. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147618 · Cited by 198
Commensal Clostridiales strains mediate effective anti-cancer immune response against solid tumors
Montalban‐Arques, A., Katkeviciutė, E., Busenhart, P., Bircher, A., Wirbel, J., Zeller, G., Morsy, Y., Borsig, L., Garzon, J. F. G., Mueller, A., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.08.001 · Cited by 200
Siderophore-mediated iron acquisition and modulation of host-bacterial interactions
Ellermann, M., & Arthur, J. C. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.489 · Cited by 186
He, B., Hoang, T. K., Wang, T., Ferris, M., Taylor, C. M., Tian, X., Luo, M., Tran, D. Q., Zhou, J., Tatevian, N., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160961 · Cited by 196
Metadata
- Authors
- Belkaid, Y., & Hand, T. W.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Belkaid, Yasmine
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2014-03
- Volume
- 157
- Issue
- 1
- Pages
- 121-141
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC4056765
- OpenAlex
- W2077553363
- Cited by
- 5,385
- References
- 258
- Citations by year
- 2026: 492 · 2025: 632 · 2024: 666 · 2023: 593 · 2022: 573 · 2021: 685 · 2020: 471 · 2019: 410 · 2018: 306 · 2017: 250 · 2016: 157 · 2015: 105 · 2014: 45
- FWCI
- 17.48
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (ZIAAI001115)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- gut microbiota, host-microbe symbiosis, immune system development, immune tolerance, inflammation, autoimmune disease, antibiotic overuse, diet, helminths, microbial diversity, immune resilience
- MeSH terms
- Animals, Anti-Bacterial Agents, Bacteria, Fungi, Humans, Immune System, Inflammation, Symbiosis, Bacterial Physiological Phenomena, Microbiota
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