4.6 Article

γδ T cell homeostasis is controlled by IL-7 and IL-15 together with subset-specific factors

Journal

JOURNAL OF IMMUNOLOGY
Volume 174, Issue 8, Pages 4606-4612

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.174.8.4606

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Funding

  1. NIAID NIH HHS [AI52257, AI32751] Funding Source: Medline
  2. NIAMS NIH HHS [AR32103, AR39555] Funding Source: Medline

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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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