Emergence of Distinct Multiarmed Immunoregulatory Antigen-Presenting Cells during Persistent Viral Infection

被引:48
作者
Wilson, Elizabeth B. [1 ,2 ]
Kidani, Yoko [3 ]
Elsaesser, Heidi [1 ,2 ]
Barnard, Jennifer [1 ,2 ]
Raff, Laura [1 ,2 ]
Karp, Christopher L. [4 ,5 ]
Bensinger, Steven [3 ]
Brooks, David G. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, AIDS Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[4] Cincinnati Childrens Hosp Med Ctr, Div Mol Immunol, Cincinnati, OH 45229 USA
[5] Univ Cincinnati, Coll Med, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
LYMPHOCYTIC CHORIOMENINGITIS VIRUS; TRANSCRIPTIONAL REPRESSOR BLIMP-1; T-CELLS; DENDRITIC CELLS; MACROPHAGE POLARIZATION; INTERLEUKIN-10; RECEPTOR; IL-10; EXHAUSTION; RESPONSES; DIFFERENTIATION;
D O I
10.1016/j.chom.2012.03.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During persistent viral infection, adaptive immune responses are suppressed by immunoregulatory factors, contributing to viral persistence. Although this suppression is mediated by inhibitory factors, the mechanisms by which virus-specific T cells encounter and integrate immunoregulatory signals during persistent infection are unclear. We show that a distinct population of IL-10-expressing immunoregulatory antigen-presenting cells (APCs) is amplified during chronic versus acute lymphocytic choriomeningitis virus (LCMV) infection and suppresses T cell responses. Although acute LCMV infection induces the expansion of immunoregulatory APCs, they subsequently decline. However, during persistent LCMV infection, immunoregulatory APCs are amplified and parallel the viral replication kinetics. Further characterization demonstrates that immunoregulatory APCs are molecularly and meta-bolically distinct, and exhibit increased expression of T cell-interacting molecules and negative regulatory factors that suppress T cell responses. Thus, immunoregulatory APCs are amplified during viral persistence and deliver inhibitory signals that suppress antiviral T cell immunity and likely contribute to persistent infection.
引用
收藏
页码:481 / 491
页数:11
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