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Segmented Filamentous Bacteria Antigens Presented by Intestinal Dendritic Cells Drive Mucosal Th17 Cell Differentiation
Open accessAbstract
How commensal microbiota contributes to immune cell homeostasis at barrier surfaces is poorly understood. Lamina propria (LP) T helper 17 (Th17) cells participate in mucosal protection and are induced by commensal segmented filamentous bacteria (SFB). Here we show that MHCII-dependent antigen presentation of SFB antigens by intestinal dendritic cells (DCs) is crucial for Th17 cell induction. Expression of MHCII on CD11c(+) cells was necessary and sufficient for SFB-induced Th17 cell differentiation. Most SFB-induced Th17 cells recognized SFB in an MHCII-dependent manner. SFB primed and induced Th17 cells locally in the LP and Th17 cell induction occurred normally in mice lacking secondary lymphoid organs. The importance of other innate cells was unveiled by the finding that MHCII deficiency in group 3 innate lymphoid cells (ILCs) resulted in an increase in SFB-independent Th17 cell differentiation. Our results outline the complex role of DCs and ILCs in the regulation of intestinal Th17 cell homeostasis.
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“presentation of SFB-derived antigens by intestinal APCs was shown to be sufficient for TH17 cell development (Goto et al., 2014; Panea et al., 2015).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Goto et al., 2014
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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
Self-citationThe 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
Korn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873
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
Induction 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
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
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
Self-citationTreg 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
Regulatory T cells: mechanisms of differentiation and function
Josefowicz, S. Z., Lu, L.-F., & Rudensky, A. Y. (2012) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141623 · Cited by 2,866
Rescigno, M., Urbano, M., Valzasina, B., Francolini, M., Rotta, G., Bonasio, R., Granucci, F., Kraehenbuhl, J.-P., & Ricciardi‐Castagnoli, P. (2001) · Nature Immunology · doi:10.1038/86373 · Cited by 2,554
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Wu, J. F., Muthusamy, A., Al‐Ghalith, G. A., Knights, D., Guo, B., Wu, B., Remmel, R. P., Schladt, D. P., Alegre, M., Oetting, W. S., et al. (2018) · Clinical Transplantation · doi:10.1111/ctr.13436 · Cited by 43
Schiavi, E., Smolińska, S., & O’Mahony, L. (2015) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000155 · Cited by 42
Ihara, S., Hirata, Y., Serizawa, T., Suzuki, N., Sakitani, K., Kinoshita, H., Hayakawa, Y., Nakagawa, H., Ijichi, H., Tateishi, K., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502548 · Cited by 42
Tolerance to the Intestinal Microbiota Mediated by ROR(γt) + Cells
Ohnmacht, C. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.05.002 · Cited by 45
Butera, A., Paola, M. D., Vitali, F., Nitto, D. D., Covotta, F., Borrini, F., Pica, R., Filippo, C. D., Cavalieri, D., Giuliani, A., et al. (2019) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjz154 · Cited by 42
Distinct Regulatory and Effector T Cell Metabolic Demands during Graft-Versus-Host Disease
Hippen, K. L., Aguilar, E. G., Rhee, S. Y., Bolivar-Wagers, S., & Blazar, B. R. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.11.005 · Cited by 44
Gut dysbiosis is associated with acceleration of lupus nephritis
Valiente, G. R., Munir, A., Hart, M. L., Blough, P., Wada, T. T., Dalan, E. E., Willis, W. L., Wu, L., Freud, A. G., & Jarjour, W. N. (2022) · Scientific Reports · doi:10.1038/s41598-021-03886-5 · Cited by 42
The Role of the Gut Microbiota in the Pathogenesis of Antiphospholipid Syndrome
Ruff, W. E., Vieira, S. M., & Kriegel, M. A. (2014) · Current Rheumatology Reports · doi:10.1007/s11926-014-0472-1 · Cited by 43
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Paun, A., & Danska, J. S. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.09.004 · Cited by 43
The crosstalk between gut bacteria and host immunity in intestinal inflammation
Yang, Q., Wang, Y., Jia, A., Wang, Y., Bi, Y., & Liu, G. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.30024 · Cited by 44
Shankar, J., Solis, N. V., Mounaud, S. H., Szpakowski, S., Liu, H., Losada, L. C., Nierman, W. C., & Filler, S. G. (2015) · Scientific Reports · doi:10.1038/srep08131 · Cited by 41
Li, Y., Yang, Y., Wang, J., Cai, P., Li, M., Tang, X., Tan, Y. C., Wang, Y., Zhang, F., Wen, X., et al. (2022) · Cellular and Molecular Immunology · doi:10.1038/s41423-022-00871-4 · Cited by 39
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Ko, H., & Chang, S. (2015) · Immune Network · doi:10.4110/in.2015.15.1.1 · Cited by 41
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Geuking, M. B., & Burkhard, R. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-00335-w · Cited by 38
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Kononova, S., Litvinova, E. A., Vakhitov, T., Skalinskaya, M. I., & Sitkin, S. I. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083854 · Cited by 41
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Bartman, C., Chong, A. S., & Alegre, M. (2015) · Current Opinion in Organ Transplantation · doi:10.1097/mot.0000000000000150 · Cited by 39
Zhang, Y., Cao, M., Li, Y., Chen, X.-X., Yu, Q., & Rui, Y. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03700-4 · Cited by 40
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Gelsinger, D. R., Ronda, C., Ma, J., Kar, O. B., Edwards, M., Huang, Y., Mavros, C. F., Sun, Y., Perdue, T., Vo, P. L. H., et al. (2025) · Science · doi:10.1126/science.adx7604 · Cited by 37
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Ge, Z., Sheh, A., Feng, Y., Muthupalani, S., Ge, L., Wang, C., Kurnick, S. A., Mannion, A. J., Whary, M. T., & Fox, J. G. (2018) · Scientific Reports · doi:10.1038/s41598-018-25927-2 · Cited by 34
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Tang, F., Deng, M., Xu, C., Yang, R., Ji, X., Hao, M., Wang, Y., Tian, M., Geng, Y., & Miao, J. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1328419 · Cited by 39
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Klüber, P., Meurer, S. K., Lambertz, J., Schwarz, R., Zechel-Gran, S., Braunschweig, T. A., Hurka, S., Domann, E., & Weiskirchen, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313156 · Cited by 31
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Park, J., & Eberl, G. (2018) · The Journal of Microbiology · doi:10.1007/s12275-018-7565-x · Cited by 32
Zhang, X., Gao, X., Liu, Z., Shao, F., Yu, D., Zhao, M., Qin, X., & Wang, S. (2024) · Nature Communications · doi:10.1038/s41467-024-48794-0 · Cited by 31
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Papa, A., Santini, P., Lucia, S. S. D., Maresca, R., Porfidia, A., Pignatelli, P., Gasbarrini, A., Violi, F., & Pola, R. (2023) · Thrombosis Research · doi:10.1016/j.thromres.2023.11.005 · Cited by 29
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Scott, C. L., Zangerle-Murray, T., Beckham, K. S. H., Douce, G. R., & Mowat, A. M. (2014) · European Journal of Immunology · doi:10.1002/eji.201444859 · Cited by 29
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Shin, C., & Kim, Y. (2019) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2019.04.018 · Cited by 30
Okamura, Y., Morimoto, N., Ikeda, D., Mizusawa, N., Watabe, S., Miyanishi, H., Saeki, Y., Takeyama, H., Aoki, T., Kinoshita, M., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00425 · Cited by 31
Brabec, T., Schwarzer, M., Kovacova, K., Dobešová, M., Schierová, D., Březina, J., Pacáková, I., Šrůtková, D., Ben‐Nun, O., Goldfarb, Y., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20230194 · Cited by 30
Burgess, S. L., Saleh, M., Cowardin, C. A., Buonomo, E. L., Noor, Z., Watanabe, K., Abhyankar, M. M., Lajoie, S., Wills-Karp, M. A., & Petri, W. A. (2016) · Infection and Immunity · doi:10.1128/iai.00316-16 · Cited by 28
Figliuolo, V. R., Jamwal, D. R., Gurney, M. A., Midura‐Kiela, M. T., Harrison, C. A., Cox, C. M., Wilson, J. M., Ghishan, F. K., & Kiela, P. R. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00304 · Cited by 29
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Umesaki, Y. (2014) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.90.313 · Cited by 28
Goc, J., Hepworth, M. R., & Sonnenberg, G. F. (2015) · International Immunology · doi:10.1093/intimm/dxv056 · Cited by 27
Lou, J., Cui, S., Li, J., Jin, G., Fan, Y., & Huang, N. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1279680 · Cited by 26
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Roberts, M. E., Bishop, J. L., Fan, X., Beer, J. L., Kum, W. W. S., Krebs, D. L., Huang, M., Gill, N., Priatel, J. J., Finlay, B. B., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302832 · Cited by 22
Yue, N., Hu, P., Tian, C., Chen, K., Zhao, H., Zhang, Y., Yao, J., Wei, Y., Li, D., & Wang, L. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s492079 · Cited by 25
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Singhi, S. C., & Jayashre, M. (2009) · PubMed · Cited by 20
Ortiz, A. M., & Brenchley, J. M. (2017) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0000000000000424 · Cited by 20
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Chen, H., Yin, Y., Wang, Y., Wang, X., & Xiang, C. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01061-17 · Cited by 19
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Royer, C. J., Rodriguez-Marino, N. C., Yaceczko, M., Rivera-Rodriguez, D. E., Ziegler, T. R., & Cervantes‐Barragán, L. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113140 · Cited by 16
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Segmental patterning of microbiota and immune cells in the murine intestinal tract
Anandakumar, H., Rauch, A., Wimmer, M. I., Yarritu, A., Koch, G., McParland, V. J., Bartolomaeus, H., & Wilck, N. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2398126 · Cited by 17
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Metadata
- Authors
- Goto, Y., Panea, C., Nakato, G., Cebula, A., Lee, C., Diez, M. G., Laufer, T. M., Ignatowicz, L., & Ivanov, I. I.
- Affiliations
- Columbia University Irving Medical Center (US)
- Augusta University (US)
- Philadelphia VA Medical Center (US)
- Corresponding author
- Ivanov, Ivaylo I.
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 40
- Issue
- 4
- Pages
- 594-607
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC4084624
- OpenAlex
- W2004714320
- Cited by
- 465
- References
- 49
- Citations by year
- 2026: 24 · 2025: 29 · 2024: 24 · 2023: 30 · 2022: 38 · 2021: 34 · 2020: 42 · 2019: 36 · 2018: 35 · 2017: 32 · 2016: 46 · 2015: 61 · 2014: 32
- FWCI
- 26.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK098378)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- segmented filamentous bacteria, Th17 cell differentiation, intestinal dendritic cells, MHC class II, antigen presentation, lamina propria, commensal microbiota, ILC3, mucosal immunity, innate lymphoid cells, secondary lymphoid organs
- MeSH terms
- Animals, Antigens, Bacterial, Histocompatibility Antigens Class II, Cell Differentiation, Cells, Cultured, Clostridium, Clostridium Infections, Dendritic Cells, Intestines, Lymphocyte Activation, Lymphocytes, Mice, Transgenic, Antigen Presentation, Mice, Knockout, Mice, Nuclear Receptor Subfamily 1, Group F, Member 3, Th17 Cells, Microbiota
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