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A Transendocytosis Perspective on the CD28/CTLA-4 Pathway
被引:28
|作者:
Soskic, Blagoje
[1
]
Qureshi, Omar S.
[2
]
Hou, Tiezheng
[3
]
Sansom, David M.
[3
]
机构:
[1] Univ Birmingham, Sch Immun & Infect, Birmingham, W Midlands, England
[2] UCB, Slough, Berks, England
[3] UCL Inst Immun & Transplantat, Royal Free Campus, London, England
来源:
基金:
英国生物技术与生命科学研究理事会;
关键词:
REGULATORY T-CELLS;
ANTIGEN-PRESENTING CELLS;
MULTIORGAN TISSUE DESTRUCTION;
FUNCTION IN-VIVO;
DENDRITIC CELLS;
PHOSPHATIDYLINOSITOL;
3-KINASE;
IMMUNOLOGICAL SYNAPSE;
CD28;
COSTIMULATION;
SURFACE EXPRESSION;
CUTTING EDGE;
D O I:
10.1016/B978-0-12-800147-9.00004-2
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
T cell activation is a key event in the adaptive immune response and vital to the generation of both cellular and humoral immunity. Activation is required not only for effective CD4 T cell responses but also to provide help for B cells and the generation of cytotoxic T cell responses. Unsurprisingly, impaired T cell activation results in infectious pathology, whereas dysregulated activation can result in autoimmunity. The decision to activate is therefore tightly regulated and the CD28/CTLA-4 pathway represents this apical decision point at the molecular level. In particular, CTLA-4 (CD152) is an essential checkpoint control for autoimmunity; however, the molecular mechanism(s) by which CTLA-4 achieves its regulatory function are not well understood, especially how it functionally intersects with the CD28 pathway. In this chapter, we review the established molecular and cellular concepts relating to CD28 and CTLA-4 biology, and attempt to integrate these by discussing the transendocytosis of ligands as a new model of CTLA-4 function.
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页码:95 / +
页数:16
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