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The Journal of Immunology, 2005, 174: 4606-4612.
Copyright © 2005 by The American Association of Immunologists

{gamma}{delta} T Cell Homeostasis Is Controlled by IL-7 and IL-15 Together with Subset-Specific Factors1

Roberto Baccala2,3, Deborah Witherden2, Rosana Gonzalez-Quintial, Wolfgang Dummer4, Charles D. Surh, Wendy L. Havran and Argyrios N. Theofilopoulos3

Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037

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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