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

Mucosal-associated invariant T (MAIT) cells are semi-invariant Vα7.2 CD161 CD4 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 CD161...

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Veröffentlicht in:The Journal of experimental medicine 2018-02, Vol.215 (2), p.459-479
Hauptverfasser: Ben Youssef, Ghada, Tourret, Marie, Salou, Marion, Ghazarian, Liana, Houdouin, Véronique, Mondot, Stanislas, Mburu, Yvonne, Lambert, Marion, Azarnoush, Saba, Diana, Jean-Sébastien, Virlouvet, Anne-Laure, Peuchmaur, Michel, Schmitz, Thomas, Dalle, Jean-Hugues, Lantz, Olivier, Biran, Valérie, Caillat-Zucman, Sophie
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Sprache:eng
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Zusammenfassung:Mucosal-associated invariant T (MAIT) cells are semi-invariant Vα7.2 CD161 CD4 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 CD161 T cell and related subset levels in infancy and after cord blood transplantation. We show that Vα7.2 and Vα7.2 CD161 T cells are generated early during gestation and likely share a common prenatal developmental program. Among cord blood Vα7.2 CD161 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 CD161 T cells acquire a memory phenotype. Only these cells expand to form the adult MAIT pool, diluting out other Vα7.2 CD161 and Vα7.2 CD161 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.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20171739