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c-MAF-dependent regulatory T cells mediate immunological tolerance to a gut pathobiont
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Abstract
Both microbial and host genetic factors contribute to the pathogenesis of autoimmune diseases. There is accumulating evidence that microbial species that potentiate chronic inflammation, as in inflammatory bowel disease, often also colonize healthy individuals. These microorganisms, including the Helicobacter species, can induce pathogenic T cells and are collectively referred to as pathobionts. However, how such T cells are constrained in healthy individuals is not yet understood. Here we report that host tolerance to a potentially pathogenic bacterium, Helicobacter hepaticus, is mediated by the induction of RORγt+FOXP3+ regulatory T (iT reg) cells that selectively restrain pro-inflammatory T helper 17 (T H 17) cells and whose function is dependent on the transcription factor c-MAF. Whereas colonization of wild-type mice by H. hepaticus promoted differentiation of RORγt-expressing microorganism-specific iT reg cells in the large intestine, in disease-susceptible IL-10-deficient mice, there was instead expansion of colitogenic T H 17 cells. Inactivation of c-MAF in the T reg cell compartment impaired differentiation and function, including IL-10 production, of bacteria-specific iT reg cells, and resulted in the accumulation of H. hepaticus-specific inflammatory T H 17 cells and spontaneous colitis. By contrast, RORγt inactivation in T reg cells had only a minor effect on the bacteria-specific T reg and T H 17 cell balance, and did not result in inflammation. Our results suggest that pathobiont-dependent inflammatory bowel disease is driven by microbiota-reactive T cells that have escaped this c-MAF-dependent mechanism of iT reg-T H 17 homeostasis.
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“This conclusion is further supported by the findings that GM-CSF+ T cells co-express a great variety of other cytokines including IL-2, IL-3, IL-4, IL-6, IL-13, IL-17A, IL-22, IFNγ, and TNF [33, 36, 76, 175].”
From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [33]
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“Hence, we propose GM-CSF expression as part of a general pathogenic program together with other pro-inflammatory molecules such as BHLHE40, IFNγ, and CXCR6 that can be induced across multiple T helper cell subsets [33, 38, 177].”
From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [33]
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Citations
Cites
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Liao, Y., Smyth, G. K., & Shi, W. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btt656 · Cited by 27,219
Adjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658
The gut microbiota shapes intestinal immune responses during health and disease
Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029
Interactions Between the Microbiota and the Immune System
Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173
Self-citationPhenotypic Analysis of Antigen-Specific T Lymphocytes
Altman, J. D., Moss, P. A. H., Goulder, P. J. R., Barouch, D. H., McHeyzer-Williams, M. G., Bell, J. I., McMichael, A. J., & Davis, M. M. (1996) · Science · doi:10.1126/science.274.5284.94 · Cited by 3,544 · cited 1×
“HH-E2 tetramer was kindly produced by the NIH Tetramer Core Facility 37 .”
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota
Atarashi, K., Tanoue, T., Oshima, K., Suda, W., Nagano, Y., Nishikawa, H., Fukuda, S., Saito, T., Narushima, S., Hase, K., et al. (2013) · Nature · doi:10.1038/nature12331 · Cited by 2,872
Role of the gut microbiota in immunity and inflammatory disease
Kamada, N., Seo, S.-U., Chen, G. Y., & Núñez, G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3430 · Cited by 2,256
Read, S., Malmström, V., & Powrie, F. M. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.2.295 · Cited by 2,206
Cited by
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Items 101–200 of 499
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Lo, B. C., Chen, G., Núñez, G., & Caruso, R. (2020) · International Immunology · doi:10.1093/intimm/dxaa079 · Cited by 90
Production and Function of Immunoglobulin A
Hand, T. W., & Reboldi, A. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-102119-074236 · Cited by 88
Mucus, commensals, and the immune system
Zhao, Q. S., & Maynard, C. L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2041342 · Cited by 91
Goubet, A.-G., Lordello, L., Alves Costa Silva, C., Peguillet, I., Gazzano, M., Mbogning-Fonkou, M. D., Thelemaque, C., Lebacle, C., Thibault, C., Audenet, F., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-0201 · Cited by 86
Fang, D., & Zhu, J. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03277-0 · Cited by 85
Immune microniches shape intestinal Treg function
Gu, Y., Bartolomé-Casado, R., Xu, C., Bertocchi, A., Janney, A., Heuberger, C., Pearson, C. F., Teichmann, S. A., Thornton, E. E., & Powrie, F. M. (2024) · Nature · doi:10.1038/s41586-024-07251-0 · Cited by 86
Osman, A., Yan, B., Li, Y., Pavelko, K. D., Quandt, J., Saadalla, A. M., Singh, M. P., Kazemian, M., Gounari, F., & Khazaie, K. (2021) · Nature Immunology · doi:10.1038/s41590-021-00987-1 · Cited by 84
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
Regulatory T‐cell development in the tumor microenvironment
Itahashi, K., Irie, T., & Nishikawa, H. (2022) · European Journal of Immunology · doi:10.1002/eji.202149358 · Cited by 86
Bianchimano, P., Britton, G. J., Wallach, D. S., Smith, E. M., Cox, L. M., Liu, S., Iwanowski, K., Weiner, H. L., Faith, J. J., Clemente, J. C., et al. (2022) · Microbiome · doi:10.1186/s40168-022-01364-2 · Cited by 83
The emerging family of RORγt+ antigen-presenting cells
Abramson, J., Dobeš, J., Lyu, M., & Sonnenberg, G. F. (2023) · Nature reviews. Immunology · doi:10.1038/s41577-023-00906-5 · Cited by 87
Chen, X., Zhang, Z., Hu, Y., Cui, J., Zhi, X., Li, X., Jiang, H., Wang, Y., Zhengrong, G., Qiu, Z., et al. (2020) · Aging and Disease · doi:10.14336/ad.2019.0613 · Cited by 81
Bilate, A. M. B., London, M., Castro, T. B. R., Mesin, L., Bortolatto, J., Kongthong, S., Harnagel, A., Victora, G. D., & Mucida, D. (2020) · Immunity · doi:10.1016/j.immuni.2020.09.003 · Cited by 79
Single-Cell Transcriptional Survey of Ileal-Anal Pouch Immune Cells From Ulcerative Colitis Patients
Devlin, J. C., Axelrad, J. E., Hine, A. M., Chang, S., Sarkar, S. A., Lin, J.-D., Ruggles, K. V., Hudesman, D. P., Cadwell, K., & Loke, P. (2021) · Gastroenterology · doi:10.1053/j.gastro.2020.12.030 · Cited by 79
c-Maf regulates the plasticity of group 3 innate lymphoid cells by restraining the type 1 program
Parker, M. E., Barrera, A., Wheaton, J. D., Zuberbuehler, M. K., Allan, D., Carlyle, J. R., Reddy, T. E., & Ciofani, M. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20191030 · Cited by 75
Commensal Bacteria-Specific CD4+ T Cell Responses in Health and Disease
Sorini, C., Cardoso, R. F., Gagliani, N., & Villablanca, E. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02667 · Cited by 77
The development of colitis in Il10 mice is dependent on IL-22
Gunasekera, D. C., Ma, J., Vacharathit, V., Shah, P. M., Ramakrishnan, A., Uprety, P., Shen, Z., Sheh, A., Brayton, C. F., Whary, M. T., et al. (2020) · Mucosal Immunology · doi:10.1038/s41385-019-0252-3 · Cited by 77
Interspecies commensal interactions have nonlinear impacts on host immunity
Rice, T., Bielecka, A. A., Nguyen, M. T., Rosen, C. E., Song, D., Sonnert, N. D., Yang, Y., Cao, Y., Khetrapal, V., Catanzaro, J., et al. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.05.004 · Cited by 75
Commensal epitopes drive differentiation of colonic T regs
Kuczma, M., Szurek, E. A., Cebula, A., Chassaing, B., Jung, Y., Kang, S., Fox, J. G., Stecher, B., & Ignatowicz, L. (2020) · Science Advances · doi:10.1126/sciadv.aaz3186 · Cited by 77
Bhattacharjee, A., Burr, A. B. P., Overacre-Delgoffe, A. E., Tometich, J. T., Yang, D., Huckestein, B. R., Linehan, J. L., Spencer, S. P., Hall, J. A., Harrison, O. J., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.07.005 · Cited by 75
Self-citationChandra, H., Sharma, K. K., Tuovinen, O. H., Sun, X., & Shukla, P. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1979882 · Cited by 83
Impact of gut microbiota on gut‐distal autoimmunity: a focus on T cells
Sprouse, M. L., Bates, N. A., Felix, K. M., & Wu, H.-J. J. (2018) · Immunology · doi:10.1111/imm.13037 · Cited by 79
Ogawa, C., Bankoti, R., Nguyen, T., Hassanzadeh‐Kiabi, N., Nadeau, S., Porritt, R. A., Couse, M., Fan, X., Dhall, D., Eberl, G., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.016 · Cited by 73
c-MAF, a Swiss Army Knife for Tolerance in Lymphocytes
Imbratta, C., Hussein, H., Andris, F., & Verdeil, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00206 · Cited by 79
PRDM16-dependent antigen-presenting cells induce tolerance to gut antigens
Fu, L., Upadhyay, R., Pokrovskii, M. V., Chen, F. M., Romero‐Meza, G., Griesemer, A., & Littman, D. R. (2025) · Nature · doi:10.1038/s41586-025-08982-4 · Cited by 81
Self-citationTranscriptional Regulation of Differentiation and Functions of Effector T Regulatory Cells
Koizumi, S.-I., & Ishikawa, H. (2019) · Cells · doi:10.3390/cells8080939 · Cited by 75
Pratama, A., Schnell, A., Mathis, D. J., & Benoist, C. O. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190428 · Cited by 74
TCF-1 limits the formation of Tc17 cells via repression of the MAF–RORγt axis
Mielke, L. A., Liao, Y., Clemens, E. B., Firth, M. A., Duckworth, B. C., Huang, Q., Almeida, F. F., Chopin, M., Koay, H., Bell, C. A., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181778 · Cited by 67
Howard, E. D., Lewis, G. M., Galle-Treger, L., Hurrell, B. P., Helou, D. G., Shafiei-Jahani, P., Painter, J. D., Muench, G. A., Soroosh, P., & Akbari, O. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.08.024 · Cited by 72
Zeng, L., Yang, K., He, Q., Zhu, X., Long, Z., Wu, Y., Chen, J., Li, Y., Zeng, J., Cui, G., et al. (2024) · BMC Medicine · doi:10.1186/s12916-024-03303-4 · Cited by 72
Zhang, X., Borbet, T. C., Fallegger, A., Wipperman, M. F., Blaser, M. J., & Mueller, A. (2021) · mBio · doi:10.1128/mbio.03335-20 · Cited by 70
Bacterial Translocation as Inflammatory Driver in Crohn’s Disease
Linares, R., Francés, R., Gutiérrez, A., & Juanola, O. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.703310 · Cited by 70
Zhang, X., Arnold, I. C., & Mueller, A. (2020) · Current Opinion in Microbiology · doi:10.1016/j.mib.2020.01.003 · Cited by 67
Alpha kinase 1 controls intestinal inflammation by suppressing the IL-12/Th1 axis
Ryzhakov, G., West, N. R., Franchini, F., Clare, S., Ilott, N. E., Sansom, S. N., Bullers, S. J., Pearson, C. F., Costain, A. H., Vaughan-Jackson, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06085-5 · Cited by 64
Engineered T cell therapy for central nervous system injury
Gao, W., Kim, M. W., Dykstra, T., Du, S., Boskovic, P., Lichti, C. F., Ruiz-Cardozo, M. A., Gu, X., Shapira, T. W., Rustenhoven, J., et al. (2024) · Nature · doi:10.1038/s41586-024-07906-y · Cited by 71
Regulation of oral immune tolerance by the microbiome in food allergy
Victor, E. S., & Chatila, T. A. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.06.001 · Cited by 64
Cas9-directed immune tolerance in humans—a model to evaluate regulatory T cells in gene therapy?
Wagner, D. L., Peter, L., & Schmueck-Henneresse, M. (2021) · Gene Therapy · doi:10.1038/s41434-021-00232-2 · Cited by 63
Rankin, L. C., Kaiser, K. A., Santos, K. D. L., Park, H., Uhlemann, A., Gray, D. H. D., & Arpaia, N. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112135 · Cited by 65
Epigenetic and transcriptional mechanisms for the regulation of IL-10
Zhang, H., & Kuchroo, V. K. (2019) · Seminars in Immunology · doi:10.1016/j.smim.2019.101324 · Cited by 65
Simone, D., Penkava, F., Ridley, A., Sansom, S. N., Al‐Mossawi, H., & Bowness, P. (2021) · Communications Biology · doi:10.1038/s42003-021-02931-3 · Cited by 63
Rengarajan, S., Knoop, K. A., Rengarajan, A., Chai, J. N., Grajales‐Reyes, J. G., Samineni, V. K., Russler-Germain, E. V., Ranganathan, P., Fasano, A., Sayuk, G. S., et al. (2020) · Cell Reports Medicine · doi:10.1016/j.xcrm.2020.100124 · Cited by 63
Pedersen, T. K., Brown, E., Plichta, D. R., Johansen, J., Twardus, S. W., Delorey, T. M., Lau, H., Vlamakis, H. C., Moon, J. J., Xavier, R. J., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.08.016 · Cited by 61
Antigen-presenting cells as specialized drivers of intestinal T cell functions
Kedmi, R., & Littman, D. R. (2024) · Immunity · doi:10.1016/j.immuni.2024.09.011 · Cited by 66
Self-citationMicrobiota-Propelled T Helper 17 Cells in Inflammatory Diseases and Cancer
Bellone, M., Brevi, A., & Huber, S. (2020) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00064-19 · Cited by 60
Wang, R., Campbell, S., Amir, M., Mosure, S. A., Bassette, M. A., Eliason, A. D., Sundrud, M. S., Kamenecka, T. M., & Solt, L. A. (2021) · Nature Communications · doi:10.1038/s41467-020-20385-9 · Cited by 58
Intestinal epithelial HDAC3 and MHC class II coordinate microbiota-specific immunity
Eshleman, E. M., Shao, T., Woo, V., Rice, T., Engleman, L., Didriksen, B. J., Whitt, J., Haslam, D. B., Way, S. S., & Alenghat, T. (2023) · Journal of Clinical Investigation · doi:10.1172/jci162190 · Cited by 57
Tissue regulatory T cells and neural repair
Ito, M., Komai, K., Nakamura, T., Srirat, T., & Yoshimura, A. (2019) · International Immunology · doi:10.1093/intimm/dxz031 · Cited by 59
Serum amyloid protein A in inflammatory bowel disease: from bench to bedside
Chen, R., Chen, Q., Zheng, J., Zeng, Z., Chen, M., Li, L., & Zhang, S. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01455-5 · Cited by 57
A wave of Thetis cells imparts tolerance to food antigens early in life
Parisotto, Y. F., Cabric, V., Park, T., Akagbosu, B., Zhao, Z., Lo, Y., Fisher, L., Shibu, G., Iza, Y. A. P., Leslie, C. S., et al. (2025) · Science · doi:10.1126/science.adp0535 · Cited by 72
T Helper 17 Cells as Pathogenic Drivers of Periodontitis
Dutzan, N., & Abusleme, L. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-28524-1_9 · Cited by 60
Wang, T., Zhou, Q., Zeng, H., Zhang, H., Liu, Z., Shao, J., Wang, Z., Xiong, Y., Wang, J., Bai, Q., et al. (2020) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-020-02583-y · Cited by 51
Lui, P. P., Cho, I., & Ali, N. (2020) · Immunology · doi:10.1111/imm.13208 · Cited by 61
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
The gut microbiota response to helminth infection depends on host sex and genotype
Ling, F., Steinel, N. C., Weber, J. N., Ma, L., Smith, C. C. R., Corrêa, D. T., Zhu, B., Bolnick, D. I., & Wang, G. (2020) · The ISME Journal · doi:10.1038/s41396-020-0589-3 · Cited by 56
Heuberger, C., Janney, A., Ilott, N. E., Bertocchi, A., Pott, S., Gu, Y., Pohin, M., Friedrich, M., Mann, E. H., Pearson, C. F., et al. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.05.001 · Cited by 55
Vân, N. T. T., Zhang, K., Wigmore, R. M., Kennedy, A., DaSilva, C. R., Huang, J., Ambelil, M., Vilagomez, J. H., O’Connor, G. J., Longman, R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43211-4 · Cited by 57
Fan, J., Zhu, J., & Xu, H. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1342913 · Cited by 55
Russler-Germain, E. V., Jung, J., Miller, A. T., Young, S., Yi, J., Wehmeier, A., Fox, L. E., Monte, K. J., Chai, J. N., Kulkarni, D. H., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.10.002 · Cited by 50
Spatiotemporal regulation of peripheral T cell tolerance
Brown, C. C., & Rudensky, A. Y. (2023) · Science · doi:10.1126/science.adg6425 · Cited by 60
Activation pathways that drive CD4 + T cells to break tolerance in autoimmune diseases*
Krovi, S. H., & Kuchroo, V. K. (2022) · Immunological Reviews · doi:10.1111/imr.13071 · Cited by 56
Synchronization of mothers and offspring promotes tolerance and limits allergy
Knoop, K. A., McDonald, K. G., Coughlin, P. E., Kulkarni, D. H., Gustafsson, J. K., Rusconi, B. A., John, V., Ndao, I. M., Beigelman, A., Good, M. L., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.137943 · Cited by 53
Potential links between the microbiota and T cell immunity determine the tumor cell fate
Mohseni, A. H., Taghinezhad‐S, S., Casolaro, V., Lv, Z., & Li, D. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05560-2 · Cited by 54
Regulation of inflammation by Interleukin-10 in the intestinal and respiratory mucosa
Branchett, W. J., Saraiva, M., & O’Garra, A. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102495 · Cited by 56
Regulatory T cell heterogeneity and therapy in autoimmune diseases
Zhang, R., Miao, J., & Zhu, P. (2020) · Autoimmunity Reviews · doi:10.1016/j.autrev.2020.102715 · Cited by 52
The role of the changing human microbiome in the asthma pandemic
Borbet, T. C., Zhang, X., Mueller, A., & Blaser, M. J. (2019) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2019.10.022 · Cited by 52
Cortés, A., Wills, J., Su, X.-P., Hewitt, R. E., Robertson, J., Scotti, R., Price, D., Bartley, Y., McNeilly, T., Krause, L., et al. (2019) · Microbiome · doi:10.1186/s40168-020-00818-9 · Cited by 45
Transcriptional regulation of adaptive and innate lymphoid lineage specification
Spinner, C. A., & Lazarevic, V. (2020) · Immunological Reviews · doi:10.1111/imr.12935 · Cited by 54
Transcription factor c‐Maf is essential for IL ‐10 gene expression in B cells
Liu, M., Zhao, X., Ma, Y., Zhou, Y., Deng, M., & Ma, Y. (2018) · Scandinavian Journal of Immunology · doi:10.1111/sji.12701 · Cited by 49
Living probiotic biomaterials for osteoporosis therapy
Chen, Z., Cai, Z., Zhuang, P., Li, F., Cui, W., & Li, Z. (2022) · Biomedical Technology · doi:10.1016/j.bmt.2022.11.007 · Cited by 49
Yoshimatsu, Y., Sujino, T., Miyamoto, K., Harada, Y., Tanemoto, S., Ono, K., Umeda, S., Yoshida, K., Teratani, T., Suzuki, T., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110773 · Cited by 48
Jensen, B. A. H., Holm, J. B., Larsen, I., von Burg, N., Derer, S., Sonne, S. B., Pærregaard, S. I., Damgaard, M. V., Indrelid, S., Rivollier, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21408-9 · Cited by 49
Stability and plasticity of regulatory T cells in health and disease
Contreras-Castillo, E., García-Rasilla, V. Y., García-Patiño, M. G., & Licona-Limón, P. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae049 · Cited by 46
Osaki, M., & Sakaguchi, S. (2025) · Immunity · doi:10.1016/j.immuni.2025.03.004 · Cited by 49
Xie, S., Cai, Y., Chen, D., Xiang, Y., Cai, W., Mao, J., & Ye, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1003419 · Cited by 45
Phenotypic and Functional Diversity in Regulatory T Cells
Sjaastad, L. E., Owen, D. L., Tracy, S. I., & Farrar, M. A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.715901 · Cited by 50
Interaction between microbiota and immunity and its implication in colorectal cancer
Xing, C., Du, Y., Duan, T., Nim, K., Chu, J., Wang, H. Y., & Wang, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.963819 · Cited by 47
Hashim, H. M., & Makpol, S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1007166 · Cited by 47
Sano, T., Kageyama, T., Fang, V., Kedmi, R., Martinez, C. S., Talbot, J., Chen, A., Cabrera, I., Gorshko, O., Kurakake, R., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109608 · Cited by 45
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Khantakova, J. N., Сергеевич, Б. А., & Sennikov, S. V. (2022) · Cells · doi:10.3390/cells11101687 · Cited by 46
Tomalka, J. A., Suthar, M. S., Deeks, S. G., & Sékaly, R. (2022) · Nature Immunology · doi:10.1038/s41590-022-01130-4 · Cited by 45
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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
Chisolm, D. A., Cheng, W. Y., Colburn, S. A., Silva-Sánchez, A., Meza‐Perez, S., Randall, T. D., & Weinmann, A. S. (2019) · Immunity · doi:10.1016/j.immuni.2019.05.006 · Cited by 43
Sun, H., Kuk, W., Rivera–Nieves, J., Lopez‐Ramirez, M. A., Eckmann, L., & Ginsberg, M. H. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.10.012 · Cited by 43
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Loo, T. T., Gao, Y., & Lazarevic, V. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.1ri0418-152rr · Cited by 43
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Victor, E. S., Kuziel, G. A., Martínez‐Blanco, M., Jugder, B., Benamar, M., Wang, Z., Chen, Q., Lozano, G. L., Abdel-Gadir, A., Cui, Y., et al. (2025) · Nature · doi:10.1038/s41586-024-08440-7 · Cited by 41
Qiu, W., Wu, H., Hu, Z., Wu, X., Tu, M., Fang, F., Zhu, X., Liu, Y., Lian, J., Valverde, P., et al. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15277 · Cited by 39
Xu, H., Wu, L., Nguyen, H. H., Mesa, K. R., Raghavan, V., Episkopou, V., & Littman, D. R. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210777 · Cited by 42
Self-citationCho, H., Jaime, H., de Oliveira, R. P., Kang, B., Spolski, R. J., Vaziri, T., Myers, T. G., Thovarai, V., Shen, Z., Fox, J. G., et al. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0056-x · Cited by 40
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Edwards, C. L., Ng, S. S., Rivera, F. D. L., Corvino, D., Engel, J. A., de, M. M., Bukali, L., Frame, T. C. M., Bunn, P. T., Chauhan, S. B., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci153733 · Cited by 42
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Iliev, I. D., Blander, J. M., Collins, N., Guo, C., Longman, R., Sonnenberg, G. F., Zeng, M. Y., & Artis, D. (2025) · Nature Immunology · doi:10.1038/s41590-025-02281-w · Cited by 55
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Geuking, M. B., & Burkhard, R. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-00335-w · Cited by 38
Chen, L., He, Z., Reis, B. S., Gelles, J. D., Chipuk, J. E., Ting, A. T., Spicer, J. A., Trapani, J. A., Furtado, G. C., & Lira, S. A. (2022) · Cellular and Molecular Immunology · doi:10.1038/s41423-022-00864-3 · Cited by 38
Yao, Y., Feng, S., Li, X., Liu, T., Ye, S., Ma, L., & Man, S. (2023) · Cell Death and Disease · doi:10.1038/s41419-022-05482-5 · Cited by 37
Fallegger, A., Priola, M., Borán, M. S., Núñez, N. G., Wild, S., Gurtner, A., Becher, B., Yousefi, S., Simon, H., Arnold, I. C., et al. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00484-0 · Cited by 38
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Distal Consequences of Mucosal Infections in Intestinal and Lung Inflammation
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Metadata
- Authors
- Xu, M., Pokrovskii, M., Ding, Y., Yi, R., Au, C., Harrison, O. J., Galan, C., Belkaid, Y., Bonneau, R., & Littman, D. R.
- Affiliations
- New York University (US)
- University of Rochester Medicine (US)
- Courant Institute of Mathematical Sciences (US)
- Howard Hughes Medical Institute (US)
- National Institutes of Health (US)
- Corresponding author
- Littman, Dan R.
- ORCID
- Venue
- Nature
- Published
- 2018-02
- Volume
- 554
- Issue
- 7692
- Pages
- 373-377
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5814346
- OpenAlex
- W2786985471
- Cited by
- 498
- References
- 50
- Citations by year
- 2026: 33 · 2025: 63 · 2024: 45 · 2023: 66 · 2022: 64 · 2021: 64 · 2020: 65 · 2019: 66 · 2018: 32
- FWCI
- 24.38
- Type
- journal article
- Language
- en
- Update notices
- correction (2019-02-05)
- Open access
- green
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Cancer Research Institute
- National Institutes of Health (1s10od018338-01, 1s10od010584-01a1)
- School of Medicine, New York University (P30CA016087)
- National Cancer Institute (P30CA016087)
- National Institute of Allergy and Infectious Diseases (T32AI100853)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK103358)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- c-Maf, regulatory T cells, Helicobacter hepaticus, pathobionts, inflammatory bowel disease, Th17 cells, IL-10, RORγt, Foxp3, gut microbiota, immune tolerance, commensal bacteria, spontaneous colitis, IL-10-deficient mice, microbiota-targeted therapy
- MeSH terms
- Animals, Colitis, Female, Homeostasis, Immune Tolerance, Intestines, Male, Interleukin-10, Helicobacter hepaticus, T-Lymphocytes, Regulatory, Proto-Oncogene Proteins c-maf, Mice, Forkhead Transcription Factors, Host-Pathogen Interactions, Bioengineering, Nuclear Receptor Subfamily 1, Group F, Member 3, Th17 Cells
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