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Publication : SLAMF7 and IL-6R define distinct cytotoxic versus helper memory CD8<sup>+</sup> T cells.

First Author  Loyal L Year  2020
Journal  Nat Commun Volume  11
Issue  1 Pages  6357
PubMed ID  33311473 Mgi Jnum  J:301416
Mgi Id  MGI:6504597 Doi  10.1038/s41467-020-19002-6
Citation  Loyal L, et al. (2020) SLAMF7 and IL-6R define distinct cytotoxic versus helper memory CD8(+) T cells. Nat Commun 11(1):6357
abstractText  The prevailing 'division of labor' concept in cellular immunity is that CD8(+) T cells primarily utilize cytotoxic functions to kill target cells, while CD4(+) T cells exert helper/inducer functions. Multiple subsets of CD4(+) memory T cells have been characterized by distinct chemokine receptor expression. Here, we demonstrate that analogous CD8(+) memory T-cell subsets exist, characterized by identical chemokine receptor expression signatures and controlled by similar generic programs. Among them, Tc2, Tc17 and Tc22 cells, in contrast to Tc1 and Tc17 + 1 cells, express IL-6R but not SLAMF7, completely lack cytotoxicity and instead display helper functions including CD40L expression. CD8(+) helper T cells exhibit a unique TCR repertoire, express genes related to skin resident memory T cells (TRM) and are altered in the inflammatory skin disease psoriasis. Our findings reveal that the conventional view of CD4(+) and CD8(+) T cell capabilities and functions in human health and disease needs to be revised.
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