| Literature DB >> 22086415 |
Lucy J Walker1, Yu-Hoi Kang, Matthew O Smith, Hannah Tharmalingham, Narayan Ramamurthy, Vicki M Fleming, Natasha Sahgal, Alistair Leslie, Ye Oo, Alessandra Geremia, Thomas J Scriba, Willem A Hanekom, Georg M Lauer, Olivier Lantz, David H Adams, Fiona Powrie, Eleanor Barnes, Paul Klenerman.
Abstract
Human mucosal associated invariant T (MAIT) CD8(+) and Tc17 cells are important tissue-homing cell populations, characterized by high expression of CD161 ((++)) and type-17 differentiation, but their origins and relationships remain poorly defined. By transcriptional and functional analyses, we demonstrate that a pool of polyclonal, precommitted type-17 CD161(++)CD8αβ(+) T cells exist in cord blood, from which a prominent MAIT cell (TCR Vα7.2(+)) population emerges post-natally. During this expansion, CD8αα T cells appear exclusively within a CD161(++)CD8(+)/MAIT subset, sharing cytokine production, chemokine-receptor expression, TCR-usage, and transcriptional profiles with their CD161(++)CD8αβ(+) counterparts. Our data demonstrate the origin and differentiation pathway of MAIT-cells from a naive type-17 precommitted CD161(++)CD8(+) T-cell pool and the distinct phenotype and function of CD8αα cells in man.Entities:
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Year: 2011 PMID: 22086415 PMCID: PMC3257008 DOI: 10.1182/blood-2011-05-353789
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113