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Ontogeny of human mucosal-associated invariant T cells and related T cell subsets

5 févr. 2018Journal of Experimental Medicine

DOI : 10.1084/jem.20171739

Auteurs

Ghada Ben Youssef, Marie Tourret, Marion Salou, Liana Ghazarian, Véronique Houdouin, Stanislas Mondot, Yvonne Mburu, Marion Lambert, Saba Azarnoush, Jean-Sébastien Diana, Anne-Laure Virlouvet, Michel Peuchmaur, Thomas Schmitz, Jean-Hugues Dalle, Olivier Lantz, Valérie Biran, Sophie Caillat-Zucman

Résumé

Mucosal-associated invariant T (MAIT) cells are semi-invariant Vα7.2+ CD161highCD4− T cells that recognize microbial riboflavin precursor derivatives such as 5-OP-RU presented by MR1. Human MAIT cells are abundant in adult blood, but there are very few in cord blood. We longitudinally studied Vα7.2+ CD161high T cell and related subset levels in infancy and after cord blood transplantation. We show that Vα7.2+ and Vα7.2− CD161high T cells are generated early during gestation and likely share a common prenatal developmental program. Among cord blood Vα7.2+ CD161high T cells, the minority recognizing MR1:5-OP-RU display a TRAV/TRBV repertoire very similar to adult MAIT cells. Within a few weeks of life, only the MR1:5-OP-RU reactive Vα7.2+ CD161high T cells acquire a memory phenotype. Only these cells expand to form the adult MAIT pool, diluting out other Vα7.2+ CD161high and Vα7.2− CD161high populations, in a process requiring at least 6 years to reach adult levels. Thus, the high clonal size of adult MAIT cells is antigen-driven and likely due to the fine specificity of the TCRαβ chains recognizing MR1-restricted microbial antigens.

Membres

OLIVIER LANTZ

Médecin

MARION SALOU

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