| Literature DB >> 28733471 |
Jiani N Chai1, Yangqing Peng1, Sunaina Rengarajan1, Benjamin D Solomon1, Teresa L Ai1, Zeli Shen2, Justin S A Perry1, Kathryn A Knoop3, Takeshi Tanoue4, Seiko Narushima4, Kenya Honda4, Charles O Elson5, Rodney D Newberry3, Thaddeus S Stappenbeck6, Andrew L Kau7, Daniel A Peterson8, James G Fox2, Chyi-Song Hsieh9.
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.Entities:
Year: 2017 PMID: 28733471 PMCID: PMC5684094 DOI: 10.1126/sciimmunol.aal5068
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468