The Control of Adaptive Immune Responses by the Innate Immune System

被引:203
作者
Schenten, Dominik [1 ,2 ]
Medzhitov, Ruslan [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06510 USA
来源
ADVANCES IN IMMUNOLOGY, VOL 109 | 2011年 / 109卷
关键词
NF-KAPPA-B; DOUBLE-STRANDED-RNA; CD4(+) T-CELLS; PYOGENIC BACTERIAL-INFECTIONS; PLASMACYTOID DENDRITIC CELLS; TOLL-LIKE RECEPTORS; GROWTH-FACTOR-BETA; CUTTING EDGE; RIG-I; HOST-DEFENSE;
D O I
10.1016/B978-0-12-387664-5.00003-0
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 mammalian immune system comprises an adaptive and an innate component. The innate immune system employs a limited number of germ-line-encoded pattern-recognition receptors (PRRs) that recognize invariant pathogen-associated molecular patterns (PAMPs). In contrast, the adaptive immune system depends on the generation of a diverse repertoire of antigen receptors on T and B lymphocytes and subsequent activation and clonal expansion of cells carrying the appropriate antigen-specific receptors. Induction of adaptive immunity not only depends on direct antigen recognition by the antigen receptors but also relies on essential signals that are delivered by the innate immune system. In recent years, we have witnessed the discovery of a still expanding array of different PRR systems that govern the generation of adaptive immunity. Here, we review our current understanding of innate control of adaptive immunity. In particular, we discuss how PRRs initiate adaptive immune responses in general, discuss specific mechanisms that shape the ensuing T and B cell responses, and highlight open questions that are still awaiting answers.
引用
收藏
页码:87 / 124
页数:38
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