Inhibition of Allograft Inflammatory Factor-1 in Dendritic Cells Restrains CD4+ T Cell Effector Responses and Induces CD25+Foxp3+ T Regulatory Subsets

被引:20
|
作者
Elizondo, Diana M. [1 ]
Andargie, Temesgen E. [1 ]
Yang, Dazhi [1 ]
Kacsinta, Apollo D. [2 ]
Lipscomb, Michael W. [1 ]
机构
[1] Howard Univ, Dept Biol, Washington, DC 20059 USA
[2] UCSD Sch Med, Dept Cellular & Mol Med, La Jolla, CA USA
来源
FRONTIERS IN IMMUNOLOGY | 2017年 / 8卷
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
dendritic cells; T regulatory cells; tolerogenic; polarization; suppression; RHEUMATOID-ARTHRITIS; MICROGLIAL CELLS; EXPRESSION; RAT; ACTIVATION; ENCEPHALOMYELITIS; IDENTIFICATION; PROLIFERATION; MACROPHAGES; EXPANSION;
D O I
10.3389/fimmu.2017.01502
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Allograft inflammatory factor-1 (AIF1) is a cytoplasmic scaffold protein shown to influence immune responses in macrophages and microglial cells. The protein contains Ca2(+) binding EF-hand and PDZ interaction domains important for mediating intracellular signaling complexes. This study now reports that AIF1 is expressed in CD11c(+) dendritic cells (DC) and silencing of expression restrains induction of antigen-specific CD4(+) T cell effector responses. AIF1 knockdown in murine DC resulted in impaired T cell proliferation and skewed polarization away from T helper type 1 and 17 fates. In turn, there was a parallel expansion of IL-10-producing and CD25(+) Foxp3(+) T regulatory subsets. These studies are the first to demonstrate that AIF1 expression in DC serves as a potent governor of cognate T cell responses and presents a novel target for engineering tolerogenic DC-based immunotherapies.
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页数:10
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