965
Views
14
CrossRef citations to date
0
Altmetric
Article Addendum

Role of SFB in autoimmune arthritis

An example of regulation of autoreactive T cell sensitivity in the gut

Pages 259-264 | Received 19 Dec 2013, Accepted 06 Feb 2014, Published online: 06 Feb 2014

References

  • Buffie CG, Pamer EG. Microbiota-mediated colonization resistance against intestinal pathogens. Nat Rev Immunol 2013; 13:790 - 801; http://dx.doi.org/10.1038/nri3535; PMID: 24096337
  • Kamada N, Seo S-U, Chen GY, Núñez G. Role of the gut microbiota in immunity and inflammatory disease. Nat Rev Immunol 2013; 13:321 - 35; http://dx.doi.org/10.1038/nri3430; PMID: 23618829
  • Mazmanian SK, Liu CH, Tzianabos AO, Kasper DL. An immunomodulatory molecule of symbiotic bacteria directs maturation of the host immune system. Cell 2005; 122:107 - 18; http://dx.doi.org/10.1016/j.cell.2005.05.007; PMID: 16009137
  • Gaboriau-Routhiau V, Rakotobe S, Lécuyer E, Mulder I, Lan A, Bridonneau C, Rochet V, Pisi A, De Paepe M, Brandi G, et al. The key role of segmented filamentous bacteria in the coordinated maturation of gut helper T cell responses. Immunity 2009; 31:677 - 89; http://dx.doi.org/10.1016/j.immuni.2009.08.020; PMID: 19833089
  • Chung H, Pamp SJ, Hill JA, Surana NK, Edelman SM, Troy EB, Reading NC, Villablanca EJ, Wang S, Mora JR, et al. Gut immune maturation depends on colonization with a host-specific microbiota. Cell 2012; 149:1578 - 93; http://dx.doi.org/10.1016/j.cell.2012.04.037; PMID: 22726443
  • Naik S, Bouladoux N, Wilhelm C, Molloy MJ, Salcedo R, Kastenmuller W, Deming C, Quinones M, Koo L, Conlan S, et al. Compartmentalized control of skin immunity by resident commensals. Science 2012; 337:1115 - 9; http://dx.doi.org/10.1126/science.1225152; PMID: 22837383
  • Cerf-Bensussan N, Gaboriau-Routhiau V. The immune system and the gut microbiota: friends or foes?. Nat Rev Immunol 2010; 10:735 - 44; http://dx.doi.org/10.1038/nri2850; PMID: 20865020
  • Klaasen HL, Koopman JP, Van den Brink ME, Bakker MH, Poelma FG, Beynen AC. Intestinal, segmented, filamentous bacteria in a wide range of vertebrate species. Lab Anim 1993; 27:141 - 50; http://dx.doi.org/10.1258/002367793780810441; PMID: 8501895
  • Yin Y, Wang Y, Zhu L, Liu W, Liao N, Jiang M, Zhu B, Yu HD, Xiang C, Wang X. Comparative analysis of the distribution of segmented filamentous bacteria in humans, mice and chickens. ISME J 2013; 7:615 - 21; http://dx.doi.org/10.1038/ismej.2012.128; PMID: 23151642
  • Schnupf P, Gaboriau-Routhiau V, Cerf-Bensussan N. Host interactions with Segmented Filamentous Bacteria: an unusual trade-off that drives the post-natal maturation of the gut immune system. Semin Immunol 2013; 25:342 - 51; http://dx.doi.org/10.1016/j.smim.2013.09.001; PMID: 24184014
  • Talham GL, Jiang HQ, Bos NA, Cebra JJ. Segmented filamentous bacteria are potent stimuli of a physiologically normal state of the murine gut mucosal immune system. Infect Immun 1999; 67:1992 - 2000; PMID: 10085047
  • Ivanov II, Atarashi K, Manel N, Brodie EL, Shima T, Karaoz U, Wei D, Goldfarb KC, Santee CA, Lynch SV, et al. Induction of intestinal Th17 cells by segmented filamentous bacteria. Cell 2009; 139:485 - 98; http://dx.doi.org/10.1016/j.cell.2009.09.033; PMID: 19836068
  • Stepankova R, Powrie F, Kofronova O, Kozakova H, Hudcovic T, Hrncir T, Uhlig H, Read S, Rehakova Z, Benada O, et al. Segmented filamentous bacteria in a defined bacterial cocktail induce intestinal inflammation in SCID mice reconstituted with CD45RBhigh CD4+ T cells. Inflamm Bowel Dis 2007; 13:1202 - 11; http://dx.doi.org/10.1002/ibd.20221; PMID: 17607724
  • Lee YK, Menezes JS, Umesaki Y, Mazmanian SK. Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis. Proc Natl Acad Sci U S A 2011; 108:Suppl 1 4615 - 22; http://dx.doi.org/10.1073/pnas.1000082107; PMID: 20660719
  • Wu H-J, Ivanov II, Darce J, Hattori K, Shima T, Umesaki Y, Littman DR, Benoist C, Mathis D. Gut-residing segmented filamentous bacteria drive autoimmune arthritis via T helper 17 cells. Immunity 2010; 32:815 - 27; http://dx.doi.org/10.1016/j.immuni.2010.06.001; PMID: 20620945
  • Chappert P, Bouladoux N, Naik S, Schwartz RH. Specific gut commensal flora locally alters T cell tuning to endogenous ligands. Immunity 2013; 38:1198 - 210; http://dx.doi.org/10.1016/j.immuni.2013.06.005; PMID: 23809163
  • Tanchot C, Barber DL, Chiodetti L, Schwartz RH. Adaptive tolerance of CD4+ T cells in vivo: multiple thresholds in response to a constant level of antigen presentation. J Immunol 2001; 167:2030 - 9; PMID: 11489985
  • Singh NJ, Chen C, Schwartz RH. The impact of T cell intrinsic antigen adaptation on peripheral immune tolerance. PLoS Biol 2006; 4:e340; http://dx.doi.org/10.1371/journal.pbio.0040340; PMID: 17048986
  • Lubberts E, Koenders MI, Oppers-Walgreen B, van den Bersselaar L, Coenen-de Roo CJJ, Joosten LAB, van den Berg WB. Treatment with a neutralizing anti-murine interleukin-17 antibody after the onset of collagen-induced arthritis reduces joint inflammation, cartilage destruction, and bone erosion. Arthritis Rheum 2004; 50:650 - 9; http://dx.doi.org/10.1002/art.20001; PMID: 14872510
  • Inobe M, Schwartz RH. CTLA-4 engagement acts as a brake on CD4+ T cell proliferation and cytokine production but is not required for tuning T cell reactivity in adaptive tolerance. J Immunol 2004; 173:7239 - 48; PMID: 15585846
  • Singh NJ, Schwartz RH. The strength of persistent antigenic stimulation modulates adaptive tolerance in peripheral CD4+ T cells. J Exp Med 2003; 198:1107 - 17; http://dx.doi.org/10.1084/jem.20030913; PMID: 14530379
  • Chiodetti L, Choi S, Barber DL, Schwartz RH. Adaptive tolerance and clonal anergy are distinct biochemical states. J Immunol 2006; 176:2279 - 91; PMID: 16455984
  • Choi S, Schwartz RH. Impairment of immunological synapse formation in adaptively tolerant T cells. J Immunol 2011; 187:805 - 16; http://dx.doi.org/10.4049/jimmunol.1003314; PMID: 21685322
  • Grossman Z, Paul WE. Adaptive cellular interactions in the immune system: the tunable activation threshold and the significance of subthreshold responses. Proc Natl Acad Sci U S A 1992; 89:10365 - 9; http://dx.doi.org/10.1073/pnas.89.21.10365; PMID: 1438221
  • Grossman Z, Paul WE. Autoreactivity, dynamic tuning and selectivity. Curr Opin Immunol 2001; 13:687 - 98; http://dx.doi.org/10.1016/S0952-7915(01)00280-1; PMID: 11677091
  • Wherry EJ. T cell exhaustion. Nat Immunol 2011; 12:492 - 9; http://dx.doi.org/10.1038/ni.2035; PMID: 21739672
  • Schwartz RH. T cell anergy. Annu Rev Immunol 2003; 21:305 - 34; http://dx.doi.org/10.1146/annurev.immunol.21.120601.141110; PMID: 12471050
  • Kinnebrew MA, Buffie CG, Diehl GE, Zenewicz LA, Leiner I, Hohl TM, Flavell RA, Littman DR, Pamer EG. Interleukin 23 production by intestinal CD103(+)CD11b(+) dendritic cells in response to bacterial flagellin enhances mucosal innate immune defense. Immunity 2012; 36:276 - 87; http://dx.doi.org/10.1016/j.immuni.2011.12.011; PMID: 22306017
  • Schlitzer A, McGovern N, Teo P, Zelante T, Atarashi K, Low D, Ho AWS, See P, Shin A, Wasan PS, et al. IRF4 transcription factor-dependent CD11b+ dendritic cells in human and mouse control mucosal IL-17 cytokine responses. Immunity 2013; 38:970 - 83; http://dx.doi.org/10.1016/j.immuni.2013.04.011; PMID: 23706669
  • Persson EK, Uronen-Hansson H, Semmrich M, Rivollier A, Hägerbrand K, Marsal J, Gudjonsson S, Håkansson U, Reizis B, Kotarsky K, et al. IRF4 transcription-factor-dependent CD103(+)CD11b(+) dendritic cells drive mucosal T helper 17 cell differentiation. Immunity 2013; 38:958 - 69; http://dx.doi.org/10.1016/j.immuni.2013.03.009; PMID: 23664832
  • Laffont S, Siddiqui KRR, Powrie F. Intestinal inflammation abrogates the tolerogenic properties of MLN CD103+ dendritic cells. Eur J Immunol 2010; 40:1877 - 83; http://dx.doi.org/10.1002/eji.200939957; PMID: 20432234
  • Ahern PP, Schiering C, Buonocore S, McGeachy MJ, Cua DJ, Maloy KJ, Powrie F. Interleukin-23 drives intestinal inflammation through direct activity on T cells. Immunity 2010; 33:279 - 88; http://dx.doi.org/10.1016/j.immuni.2010.08.010; PMID: 20732640
  • DePaolo RW, Abadie V, Tang F, Fehlner-Peach H, Hall JA, Wang W, Marietta EV, Kasarda DD, Waldmann TA, Murray JA, et al. Co-adjuvant effects of retinoic acid and IL-15 induce inflammatory immunity to dietary antigens. Nature 2011; 471:220 - 4; http://dx.doi.org/10.1038/nature09849; PMID: 21307853
  • Maccioni M, Zeder-Lutz G, Huang H, Ebel C, Gerber P, Hergueux J, Marchal P, Duchatelle V, Degott C, van Regenmortel M, et al. Arthritogenic monoclonal antibodies from K/BxN mice. J Exp Med 2002; 195:1071 - 7; http://dx.doi.org/10.1084/jem.20011941; PMID: 11956298
  • Suzuki K, Meek B, Doi Y, Muramatsu M, Chiba T, Honjo T, Fagarasan S. Aberrant expansion of segmented filamentous bacteria in IgA-deficient gut. Proc Natl Acad Sci U S A 2004; 101:1981 - 6; http://dx.doi.org/10.1073/pnas.0307317101; PMID: 14766966
  • Singh NJ, Bando JK, Schwartz RH. Subsets of nonclonal neighboring CD4+ T cells specifically regulate the frequency of individual antigen-reactive T cells. Immunity 2012; 37:735 - 46; http://dx.doi.org/10.1016/j.immuni.2012.08.008; PMID: 23021952
  • Sofi MH, Gudi R, Karumuthil-Melethil S, Perez N, Johnson BM, Vasu C. pH of Drinking Water Influences the Composition of Gut Microbiome and Type 1 Diabetes Incidence. Diabetes 2014; 63:632 - 44; http://dx.doi.org/10.2337/db13-0981; PMID: 24194504
  • Viaud S, Saccheri F, Mignot G, Yamazaki T, Daillère R, Hannani D, Enot DP, Pfirschke C, Engblom C, Pittet MJ, et al. The intestinal microbiota modulates the anticancer immune effects of cyclophosphamide. Science 2013; 342:971 - 6; http://dx.doi.org/10.1126/science.1240537; PMID: 24264990
  • Oxenius A, Zinkernagel RM, Hengartner H. Comparison of activation versus induction of unresponsiveness of virus-specific CD4+ and CD8+ T cells upon acute versus persistent viral infection. Immunity 1998; 9:449 - 57; http://dx.doi.org/10.1016/S1074-7613(00)80628-7; PMID: 9806631
  • Zajac AJ, Blattman JN, Murali-Krishna K, Sourdive DJ, Suresh M, Altman JD, Ahmed R. Viral immune evasion due to persistence of activated T cells without effector function. J Exp Med 1998; 188:2205 - 13; http://dx.doi.org/10.1084/jem.188.12.2205; PMID: 9858507
  • Staveley-O’Carroll K, Sotomayor E, Montgomery J, Borrello I, Hwang L, Fein S, Pardoll D, Levitsky H. Induction of antigen-specific T cell anergy: An early event in the course of tumor progression. Proc Natl Acad Sci U S A 1998; 95:1178 - 83; http://dx.doi.org/10.1073/pnas.95.3.1178; PMID: 9448305

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.