IL-7 is critical for homeostatic proliferation and survival of naïve T cells

Joyce T. Tan(University of Southern California), Eric Dudl(University of Southern California), Eric M. Leroy(University of Southern California), Richard M. Murray(University of Southern California), Jonathan Sprent(University of Southern California), Kenneth I. Weinberg(University of Southern California), Charles D. Surh(University of Southern California)
Proceedings of the National Academy of Sciences
July 10, 2001
Cited by 952Open Access
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Abstract

In T cell-deficient conditions, naive T cells undergo spontaneous "homeostatic" proliferation in response to contact with self-MHC/peptide ligands. With the aid of an in vitro system, we show here that homeostatic proliferation is also cytokine-dependent. The cytokines IL-4, IL-7, and IL-15 enhanced homeostatic proliferation of naive T cells in vitro. Of these cytokines, only IL-7 was found to be critical; thus, naive T cells underwent homeostatic proliferation in IL-4(-) and IL-15(-) hosts but proliferated minimally in IL-7(-) hosts. In addition to homeostatic proliferation, the prolonged survival of naive T cells requires IL-7. Thus, naïve T cells disappeared gradually over a 1-month period upon adoptive transfer into IL-7(-) hosts. These findings indicate that naive T cells depend on IL-7 for survival and homeostatic proliferation.


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