共 298 条
Regulation of antigen presentation and cross-presentation in the dendritic cell network: Facts, hypothesis, and immunological implications
被引:126
作者:

Wilson, NS
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h-index: 0
机构:
Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3050, Australia Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3050, Australia

Villadangos, JA
论文数: 0 引用数: 0
h-index: 0
机构: Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3050, Australia
机构:
[1] Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3050, Australia
[2] Walter & Eliza Hall Inst Med Res, Cooperat Res Ctr Vaccine Technol, Parkville, Vic 3050, Australia
来源:
ADVANCES IN IMMUNOLOGY, VOL 86
|
2005年
/
86卷
基金:
英国医学研究理事会;
关键词:
D O I:
10.1016/S0065-2776(04)86007-3
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Dendritic cells (DCs) are central to the maintenance of immunological tolerance and the initiation and control of immunity. The antigen-presenting properties of DCs enable them to present a sample of self and foreign proteins, contained within an organism at any given time, to the T-cell repertoire. DCs achieve this communication with T cells by displaying antigenic peptides bound to MHC I and MHC II molecules. Here we review the studies carried out over the past 15 years to characterize these antigen presentation mechanism, emphasizing their significance in relation to DC function in vivo. The life cycles of different DC populations found in vivo are described. Furthermore, we provide a critical assessment Of the studies that examine the mechanisms controlling DC MHC class II antigen presentation, which have often reached contradictory conclusions. Finally, we review findings pertaining to the biological mechanisms that enable DCs to present exogenous antigens on their MHC class I molecules, a process known as cross-presentation. Throughout, we highlight what we consider to be major knowledge gaps in the field and speculate on possible directions for future research.
引用
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页码:241 / 305
页数:65
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