Double positive thymocytes select mucosal-associated invariant T cells

Natalie Louise Seach, Lucia Guerri, Lionel Le Bourhis, Yvonne Mburu, Yue Cui, Stephanie Bessoles, Claire Soudais, Olivier Lantz

Research output: Contribution to journalArticleResearchpeer-review

77 Citations (Scopus)

Abstract

NKT and mucosal-associated invariant T (MAIT) cells express semi-invariant TCR and restriction by nonclassical MHC class Ib molecules. Despite common features, the respective development of NKT and MAIT subsets is distinct. NKTs proliferate extensively and acquire effector properties prior to thymic export. MAIT cells exit the thymus as naive cells and acquire an effector/memory phenotype in a process requiring both commensal flora and B cells. During thymic development, NKTs are selected by CD1d-expressing cortical thymocytes; however, the hematopoietic cell type responsible for MAIT cell selection remains unresolved. Using reaggregated thymic organ culture and bone marrow chimeras, we demonstrate that positive selection of mouse iValpha19 transgenic and Vbeta6 transgenic MAIT cell progenitors requires MHC-related 1-expressing CD4(+)CD8(+) double positive thymocytes, whereas thymic B cells, macrophages, and dendritic cell subsets are dispensable. Preincubation of double positive thymocytes with exogenous bacterial ligand increases MHC-related 1 surface expression and enhances mature MAIT cell activation in the in vitro cocultures. The revelation of a common cell type for the selection of both NKT and MAIT subsets raises questions about the mechanisms underlying acquisition of their specific features.
Original languageEnglish
Pages (from-to)6002 - 6009
Number of pages8
JournalJournal of Immunology
Volume191
Issue number12
DOIs
Publication statusPublished - 2013

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