@article{abbb1b176d0349ef85d3a2af0f02f407,
title = "Helicobacter species are potent drivers of colonic T cell responses in homeostasis and inflammation",
abstract = "Specific gut commensal bacteria improve host health by eliciting mutualistic regulatory T (Treg) cell responses. However, the bacteria that induce effector T (Teff) cells during inflammation are unclear. We addressed this by analyzing bacterial-reactive T cell receptor (TCR) transgenic cells and TCR repertoires in a murine colitis model. Unexpectedly, we found that mucosal-associated Helicobacter species triggered both Treg cell responses during homeostasis and Teff cell responses during colitis, as suggested by an increased overlap between the Teff/Treg TCR repertoires with colitis. Four of six Treg TCRs tested recognized mucosal-associated Helicobacter species in vitro and in vivo. By contrast, the marked expansion of luminal Bacteroides species seen during colitis did not trigger a commensurate Teff cell response. Unlike other Treg cell–inducing bacteria, Helicobacter species are known pathobionts and cause disease in immunodeficient mice. Thus, our study suggests a model in which mucosal bacteria elicit context-dependent Treg or Teff cell responses to facilitate intestinal tolerance or inflammation.",
author = "Chai, {Jiani N.} and Yangqing Peng and Sunaina Rengarajan and Solomon, {Benjamin D.} and Ai, {Teresa L.} and Zeli Shen and Perry, {Justin S.A.} and Knoop, {Kathryn A.} and Takeshi Tanoue and Seiko Narushima and Kenya Honda and Elson, {Charles O.} and Newberry, {Rodney D.} and Stappenbeck, {Thaddeus S.} and Kau, {Andrew L.} and Peterson, {Daniel A.} and Fox, {James G.} and Hsieh, {Chyi Song}",
note = "Funding Information: We thank N. Santacruz and C.‐W. Lai (Washington University) for expert technical assistance, T. Egawa and B. Kim (Washington University) for critical reading of the manuscript and advice, A. Rudensky (Memorial Sloan Kettering Cancer Center) and R. Locksley (University of California, San Francisco) for gifts of mice, and the Washington University Digestive Diseases Research Center (DDRCC) Morphology Core and the Washington University School of Medicine Developmental Biology Histology Core for technical support. C.-S.H. is supported by the NIH (DK094995 and AI079187), the Crohn{\textquoteright}s and Colitis Foundation of America, and the Burroughs Wellcome Fund. J.G.F. is supported by P30ES 002109 and T32OD10978-29. A.L.K. is supported by the NIH (K08 AI113184) and the American Academy of Allergy, Asthma and Immunology Foundation. The Washington University DDRCC Morphology Core is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK P30) and NIH (DK052574). Publisher Copyright: Copyright {\textcopyright} 2017 The Authors.",
year = "2017",
doi = "10.1126/sciimmunol.aal5068",
language = "English",
volume = "2",
journal = "Science immunology",
issn = "2470-9468",
publisher = "American Association for the Advancement of Science",
number = "13",
}