Effector V gamma 9V delta 2 T cells dominate the human fetal gamma delta T-cell repertoire
gamma delta T cells are unconventional T cells recognizing antigens via their gamma delta T-cell receptor (TCR) in a way that is fundamentally different from conventional alpha beta T cells. gamma delta T cells usually are divided into subsets according the type of V gamma and/or V... chain they exp...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2015-02, Vol.112 (6), p.E556-E556 |
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Sprache: | eng |
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Zusammenfassung: | gamma delta T cells are unconventional T cells recognizing antigens via their gamma delta T-cell receptor (TCR) in a way that is fundamentally different from conventional alpha beta T cells. gamma delta T cells usually are divided into subsets according the type of V gamma and/or V... chain they express in their TCR. T cells expressing the TCR containing the gamma -chain variable region 9 and the delta -chain variable region 2 (V gamma 9V delta 2 T cells) are the predominant gamma delta T-cell subset in human adult peripheral blood. The current thought is that this predominance is the result of the postnatal expansion of cells expressing particular complementary-determining region 3 (CDR3) in response to encounters with microbes, especially those generating phosphoantigens derived from the 2-C-methyl-d-erythritol 4-phosphate pathway of isoprenoid synthesis. However, here we show that, rather than requiring postnatal microbial exposure, V gamma 9V delta 2 T cells are the predominant blood subset in the second-trimester fetus, whereas V delta 1+ and V delta 3+ gamma delta T cells are present only at low frequencies at this gestational time. Fetal blood V gamma 9V delta 2 T cells are phosphoantigen responsive and display very limited diversity in the CDR3 of the V gamma 9 chain gene, where a germline-encoded sequence accounts for >50% of all sequences, in association with a prototypic CDR3 delta 2. Furthermore, these fetal blood V gamma 9V delta 2 T cells are functionally preprogrammed (e.g., IFN- gamma and granzymes-A/K), with properties of rapidly activatable innatelike T cells. Thus, enrichment for phosphoantigen-responsive effector T cells has occurred within the fetus before postnatal microbial exposure. These various characteristics have been linked in the mouse to the action of selecting elements and would establish a much stronger parallel between human and murine gamma delta T cells than is usually articulated. (ProQuest: ... denotes formulae/symbols omitted.) |
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ISSN: | 0027-8424 |
DOI: | 10.1073/pnas.1412058112 |