Homeostatic Expansion Occurs Independently of Costimulatory Signals
Author(s) -
Martin Prlic,
Bruce R. Blazar,
Alexander Khoruts,
Traci Zell,
Stephen C. Jameson
Publication year - 2001
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.167.10.5664
Subject(s) - homeostasis , cd28 , biology , microbiology and biotechnology , endogeny , il 2 receptor , t cell receptor , t cell , cd8 , cytotoxic t cell , immune system , immunology , genetics , endocrinology , in vitro
Naive T cells undergo homeostatic proliferation in lymphopenic mice, a process that involves TCR recognition of specific self peptide/MHC complexes. Since costimulation signals regulate the T cell response to foreign Ags, we asked whether they also regulate homeostatic expansion. We report in this study that homeostatic expansion of CD4 and CD8 T cells occurs independently of costimulation signals mediated through CD28/B7, CD40L/CD40, or 4-1BB/4-1BBL interactions. Using DO11.10 TCR transgenic T cells, we confirmed that CD28 expression was dispensable for homeostatic expansion, and showed that the presence of endogenous CD4(+)CD25(+) regulatory cells did not detectably influence homeostatic expansion. The implications of these findings with respect to regulation of T cell homeostasis and autoimmunity are discussed.
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