Early T-bet promotes LFA1 upregulation required for CD8+ effector and memory T cell development

被引:5
作者
Pritchard, Gretchen Harms [1 ]
Phan, Anthony T. [1 ]
Christian, David A. [1 ]
Blain, Trevor J. [2 ]
Fang, Qun [1 ]
Johnson, John [1 ]
Roy, Nathan H. [3 ,4 ]
Shallberg, Lindsey [1 ]
Kedl, Ross M. [2 ]
Hunter, Christopher A. [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
[2] Univ Colorado Denver, Sch Med, Dept Immunol & Microbiol, Aurora, CO USA
[3] Univ Penn, Childrens Hosp Philadelphia, Res Inst, Dept Pathol & Lab Med, Philadelphia, PA USA
[4] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
关键词
IFN-GAMMA PRODUCTION; TOXOPLASMA-GONDII INFECTION; TRANSCRIPTION FACTOR; DENDRITIC CELL; PROTECTIVE IMMUNITY; DIFFERENTIATION; EXPRESSION; RESPONSES; CD4; LYMPHOCYTES;
D O I
10.1084/jem.20191287
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T-box transcription factor T-bet is regarded as a "master regulator" of CD4(+) Th1 differentiation and IFN-gamma production. However, in multiple models of infection, T-bet appears less critical for CD8(+). T cell expansion and effector function. Here, we show that following vaccination with a replication-deficient strain of Toxoplasma gondii, CD8(+). T cell expression of T-bet is required for optimal expansion of parasite-specific effector CD8(+). T cells. Analysis of the early events associated with T cell activation reveals that the alpha chain of LFA1, CD11a, is a target of T-bet, and T-bet is necessary for CD8(+). T cell upregulation of this integrin, which influences the initial priming of CD8(+). effector T cells. We propose that the early expression of T-bet represents a T cell-intrinsic factor that optimizes T-DC interactions necessary to generate effector responses.
引用
收藏
页数:15
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