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 |
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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. |
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ISSN: | 0022-1007 1540-9538 |
DOI: | 10.1084/jem.20171739 |