Journal article
STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and function
RP Wilson, ML Ives, G Rao, A Lau, K Payne, M Kobayashi, PD Arkwright, J Peake, M Wong, S Adelstein, JM Smart, MA French, DA Fulcher, C Picard, J Bustamante, S Boisson-Dupuis, P Gray, P Stepensky, K Warnatz, AF Freeman Show all
Journal of Experimental Medicine | Published : 2015
DOI: 10.1084/jem.20141992
Abstract
Unconventional T cells such as γδ T cells, natural killer T cells (NKT cells) and mucosal-associated invariant T cells (MAIT cells) are a major component of the immune system; however, the cytokine signaling pathways that control their development and function in humans are unknown. Primary immunodeficiencies caused by single gene mutations provide a unique opportunity to investigate the role of specific molecules in regulating human lymphocyte development and function. We found that individuals with loss-of-function mutations in STAT3 had reduced numbers of peripheral blood MAIT and NKT but not γδ T cells. Analysis of STAT3 mosaic individuals revealed that this effect was cell intrinsic. Su..
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Awarded by Rockefeller University
Funding Acknowledgements
This work was funded by project and program grants from the National Health and Medical Research Council (NHMRC) of Australia (1016953, 1066694, and 1027400 to E.K. Deenick and S.G. Tangye) and the Rockefeller University Center for 541 Clinical and Translational Science (5UL1RR024143 to J.-L. Casanova). C.S. Ma is a recipient of a Career Development Fellowship (1008820), and S.G. Tangye is a recipient of a Principal Research Fellowship (1042925) from the NHMRC of Australia.