共 60 条
Competition for self ligands restrains homeostatic proliferation of naive CD4 T cells
被引:103
作者:

Moses, CT
论文数: 0 引用数: 0
h-index: 0
机构: Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA

Thorstenson, KM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA

Jameson, SC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA

Khoruts, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
机构:
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
来源:
关键词:
D O I:
10.1073/pnas.0334572100
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:
T cell antigen receptor (TCR) diversity is a critical feature of adaptive immunity. However, restriction of TCR diversity is a potential risk during immune reconstitution by homeostatic proliferation. What peripheral mechanisms are in place to maintain TCR diversity during recovery from lymphopenia? Here, we examine competition between several monoclonal CD4 T cell populations in RAG(-/-) and TCR Tg RAG(-/-) environments. The results suggest that specific self ligands constitute a critical limiting resource essential for homeostatic proliferation of naive CD4 T cells. In addition, T cells ignore large numbers of competitors as long as their TCR specificity is different and other non-MHC resources are not limiting. Therefore, the numbers of self ligands expressed in the periphery set the limits on TCR diversity.
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页码:1185 / 1190
页数:6
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