Sulfated bile acid is a host-derived ligand for MAIT cells

Author:

Ito Emi12ORCID,Inuki Shinsuke3ORCID,Izumi Yoshihiro4ORCID,Takahashi Masatomo4ORCID,Dambayashi Yuki3,Ciacchi Lisa5ORCID,Awad Wael5ORCID,Takeyama Ami12,Shibata Kensuke6ORCID,Mori Shotaro12,Mak Jeffrey Y. W.7ORCID,Fairlie David P.7ORCID,Bamba Takeshi4ORCID,Ishikawa Eri12,Nagae Masamichi12ORCID,Rossjohn Jamie58ORCID,Yamasaki Sho129ORCID

Affiliation:

1. Department of Molecular Immunology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.

2. Laboratory of Molecular Immunology, Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan.

3. Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Kyoto 606-8501, Japan.

4. Division of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka 812-8582, Japan.

5. Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.

6. Department of Microbiology and Immunology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan.

7. Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland 4072, Australia.

8. Institute of Infection and Immunity, Cardiff University, School of Medicine, Heath Park, Cardiff, UK.

9. Center for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, 565-0871, Japan.

Abstract

Mucosal-associated invariant T (MAIT) cells are innate-like T cells that recognize bacterial riboflavin–based metabolites as activating antigens. Although MAIT cells are found in tissues, it is unknown whether any host tissue–derived antigens exist. Here, we report that a sulfated bile acid, cholic acid 7-sulfate (CA7S), binds the nonclassical MHC class I protein MR1 and is recognized by MAIT cells. CA7S is a host-derived metabolite whose levels were reduced by more than 98% in germ-free mice. Deletion of the sulfotransferase 2a family of enzymes ( Sult2a1-8 ) responsible for CA7S synthesis reduced the number of thymic MAIT cells in mice. Moreover, recognition of CA7S induced MAIT cell survival and the expression of a homeostatic gene signature. By contrast, recognition of a previously described foreign antigen, 5-(2-oxopropylideneamino)-6- d -ribitylaminouracil (5-OP-RU), drove MAIT cell proliferation and the expression of inflammatory genes. Thus, CA7S is an endogenous antigen for MAIT cells, which promotes their development and function.

Publisher

American Association for the Advancement of Science (AAAS)

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