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Gamma delta T cell homeostasis is controlled by IL-7 and IL-15 together with subset-specific factors
Authors:Baccala Roberto  Witherden Deborah  Gonzalez-Quintial Rosana  Dummer Wolfgang  Surh Charles D  Havran Wendy L  Theofilopoulos Argyrios N
Affiliation:Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA. rbaccala@scripps.edu
Abstract:Among T cell subsets, gamma delta T cells uniquely display an Ag receptor-based tissue distribution, but what defines their preferential homing and homeostasis is unknown. To address this question, we studied the resources that control gamma delta T cell homeostasis in secondary lymphoid organs. We found that gamma delta and alpha beta T cells are controlled by partially overlapping resources, because acute homeostatic proliferation of gamma delta T cells was inhibited by an intact alpha beta T cell compartment, and both populations were dependent on IL-7 and IL-15. Significantly, to undergo acute homeostatic proliferation, gamma delta T cells also required their own depletion. Thus, gamma delta T cell homeostasis is maintained by trophic cytokines commonly used by other types of lymphoid cells, as well as by additional, as yet unidentified, gamma delta-specific factors.
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