CD137, implications in immunity and potential for therapy

被引:44
作者
Thum, Elaine
Zhe, Shao
Schwarz, Herbert
机构
[1] Natl Univ Singapore, Dept Physiol, Singapore 117456, Singapore
[2] Natl Univ Singapore, Immunol Programme, Yong Loo Lin Sch Med, Singapore 117456, Singapore
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词
CD137; 4-1BB; Antibody; Immunotherapy; Cancer; Tumor; Autoimmune Disease; OX40; Review; CD8; T-CELLS; FACTOR RECEPTOR FAMILY; HUMAN DENDRITIC CELLS; VERSUS-HOST-DISEASE; 4-1BB LIGAND; MONOCLONAL-ANTIBODIES; SOLUBLE CD137; IN-VIVO; COSTIMULATORY MOLECULE; LYMPHOCYTE-ACTIVATION;
D O I
10.2741/3521
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CD137 is a member of the TNF receptor family and a potent T cell costimulatory molecule. Crosslinking of CD137 on activated T cells has shown promise in enhancing anti-tumor immune responses in murine models, and agonistic anti-CD137 antibodies are currently being tested in phase I clinical trials. Surprisingly, these very same agonistic anti-CD137 antibodies have also been found to ameliorate autoimmune disease under certain circumstances. At the current state of knowledge these circumstances cannot be clearly defined. Therefore, anti-CD137 antibodies in man will need to be used with caution. CD137 ligand is expressed by antigen presenting cells. Antagonistic anti-CD137 ligand antibodies have shown efficacy in dampening disease in murine autoimmune models. A similar effect would be expected from antagonistic anti-CD137 antibodies, soluble CD137, or any other compound interfering with CD137 / CD137 ligand interaction. CD137 ligand is expressed as a transmembrane protein on the cell surface and it too can transmit signals into antigen presenting cells. Agonistic anti-CD137 ligand antibodies or a recombinant CD137 protein could stimulate the activity of antigen presenting cells.
引用
收藏
页码:4173 / 4188
页数:16
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