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

被引:780
|
作者
Tan, JT
Dudl, E
LeRoy, E
Murray, R
Sprent, J
Weinberg, KI
Surh, CD [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] Univ So Calif, Childrens Hosp, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90027 USA
[3] Univ So Calif, Childrens Hosp, Keck Sch Med, Dept Pediat, Los Angeles, CA 90027 USA
[4] Eos Biotechnol, San Francisco, CA 94080 USA
关键词
D O I
10.1073/pnas.161126098
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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, naive 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.
引用
收藏
页码:8732 / 8737
页数:6
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