MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution

Shouxiong Huang, Emmanuel Martin, Sojung Kim, Lawrence Yu, Claire Soudais, Daved H. Fremont, Olivier Lantz, Ted H. Hansen

Research output: Contribution to journalArticlepeer-review

143 Scopus citations


Several nonclassical major histocompatibilty antigens (class lb molecules) have emerged as key players in the early immune response to pathogens or stress. Class lb molecules activate subsets of T cells that mount effector responses before the adaptive immune system, and thus are called innate T cells. MR1 is a novel class lb molecule with properties highly suggestive of its regulation of mucosal immunity. The Mr1 gene is evolutionary conserved, is non-Mhc linked, and controls the development of mucosal-associated invariant T (MAIT) cells. MAIT cells preferentially reside in the gut and their development is dependent on commensal microbiota. Although these properties suggest that MAIT cells function as innate T cells in the mucosa, this has been difficult to test, due to the (i) paucity of MAIT cells that display MR1-specific activation in vitro and (ii) lack of knowledge of whether or not MR1 presents antigen. Here we show that both mouse and human MAIT cells display a high level of cross-reactivity on mammalian MR1 orthologs, but with differences consistent with limited ligand discrimination. Furthermore, acid eluates from recombinant or cellular MR1 proteins enhance MAIT cell activation in an MR1-specific and cross-species manner. Our findings demonstrate that the presentation pathway of MR1 to MAIT cells is highly evolutionarily conserved.

Original languageEnglish
Pages (from-to)8290-8295
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number20
StatePublished - May 19 2009


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