Role of 4-1BB:4-1BB ligand in cancer immunotherapy

被引:113
作者
Cheuk, ATC [1 ]
Mufti, GJ [1 ]
Guinn, BA [1 ]
机构
[1] Kings Coll London, Guys Kings & St Thomas Sch Med, Rayne Inst, Dept Haematol Med,Leukaemia Sci Labs, London SE5 9NU, England
关键词
4-1BB; costimulatory molecules; cancer immunotherapy;
D O I
10.1038/sj.cgt.7700670
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The activation of T cells plays a central role in antitumor immunity. In order to activate naive T cells, two key signals are required. Signal one is provided through the T-cell receptor (TCR) while signal two is that of costimulation. The CD28:B7 molecules are one of the best-studied costimulatory pathways, thought to be the main mechanism through which primary T-cell stimulation occurs. However, a number of molecules have been identified which serve to amplify and diversify the T-cell response, following initial T-cell activation. These include the more recently described 4-1BB:4-1BB ligand (4-1BBL) molecules. 4-1BB:4-1BBL are a member of the TNFR: TNF ligand family, which are expressed on T cells and antigen-presenting cells (APCs), respectively. Therapies utilizing the 4-1BB:4-1BBL signaling pathway have been shown to have antitumor effects in a number of model systems. In this paper, we focus on the 4-1BB: 4-1BBL costimulatory molecules. In particular, we will describe the structure and function of the 4-1BB molecule, its receptor and how 4-1BB:4-1BBL costimulation has and may be used for the immunotherapy of cancer.
引用
收藏
页码:215 / 226
页数:12
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