CD28: A New Drug Target for Immune Disease

被引:18
|
作者
Xia, Sijing [1 ]
Chen, Qin [1 ]
Niu, Bing [1 ]
机构
[1] Shanghai Univ, Coll Life Sci, 99 Shang Da Rd, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
CD28; CTLA-4; T cell activation; ligand; immune-responses; costimulation; human disease; NECROSIS-FACTOR-ALPHA; COUNTER-RECEPTORS CD80; T-CELL PROLIFERATION; LUPUS NEPHRITIS; CD28-MEDIATED COSTIMULATION; CO-STIMULATION; DOUBLE-BLIND; B7; FAMILY; IN-VIVO; CTLA-4;
D O I
10.2174/1389450120666191114102830
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: CD28, a cell surface glycoprotein receptor, predominantly expressed on activated T cells, belongs to the Ig superfamily and provides a critical co-stimulatory signal. CTLA-4 has sequence homology to CD28, and is expressed on T cells after activation. It provides an inhibition signal coordinated with CD28 to regulate T cell activation. Both of them regulate T cell proliferation and differentiation and play an important role in the immune response pathway in vivo. Objective: We studied the special role of different structural sites of CD28 in producing costimulatory signals. Methods: We reviewed the relevant literature, mainly regarding the structure of CD28 to clarify its biological function, and its role in the immune response. Results: In recent years, increasingly attention has been paid to CD28, which is considered as a key therapeutic target for many modern diseases, especially some immune diseases. Conclusion: In this paper, we mainly introduce the structure of CD28 and its related biological functions, as well as the application of costimulatory pathways targeting CD28 in disease treatment.
引用
收藏
页码:589 / 598
页数:10
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