Immunological adjuvants promote activated T cell survival via induction of Bcl-3

被引:188
作者
Mitchell, TC
Hildeman, D
Kedl, RM
Teague, TK
Schaefer, BC
White, J
Zhu, YN
Kappler, J
Marrack, P [1 ]
机构
[1] Howard Hughes Med Inst, Denver, CO 80206 USA
[2] Natl Jewish Med & Res Ctr, Dept Immunol, Denver, CO 80206 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80206 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80206 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Biochem & Mol Genet, Denver, CO 80206 USA
关键词
D O I
10.1038/87692
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Injection of soluble protein antigen into animals causes abortive proliferation of the responding T cells. Immunological adjuvants boost T cell responses at least in part by increasing the survival of activated T cells during and after the initial proliferative phase of their clonal expansion,To understand how adjuvants promote T cell survival, we used gene microarrays to analyze gene expression in T cells activated either with antigen alone or in the presence of two different adjuvants. Among the genes whose expression was increased by both adjuvants was the I kappaB family member Bcl-3. Retroviral infection experiments showed that expression of Bcl-3 increased survival of activated T cells in vitro and in vivo. Adjuvants may therefore improve survival of activated T cells via induction of Bcl-3.
引用
收藏
页码:397 / 402
页数:6
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