Immunotherapy of Cancer with 4-1BB

被引:144
作者
Vinay, Dass S. [1 ]
Kwon, Byoung S. [1 ,2 ,3 ]
机构
[1] Tulane Univ, Hlth Sci Ctr, Dept Med, Sect Clin Immunol Allergy & Rheumatol, New Orleans, LA 70112 USA
[2] Natl Canc Ctr, Div Cell & Immunobiol, Ilsan, South Korea
[3] Natl Canc Ctr, R&D Ctr Canc Therapeut, Ilsan, South Korea
关键词
ANTI-4-1BB MONOCLONAL-ANTIBODY; T-CELL-ACTIVATION; ACUTE MYELOID-LEUKEMIA; IL-12; GENE-THERAPY; CD137; LIGAND; IN-VIVO; IMMUNE-RESPONSES; TUMOR XENOGRAFTS; DENDRITIC CELLS; COSTIMULATION;
D O I
10.1158/1535-7163.MCT-11-0677
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
4-1BB (CD137), a member of the TNF receptor superfamily, is an activation-induced T-cell costimulatory molecule. Signaling via 4-1BB upregulates survival genes, enhances cell division, induces cytokine production, and prevents activation-induced cell death in T cells. The importance of the 4-1BB pathway has been underscored in a number of diseases, including cancer. Growing evidence indicates that anti-4-1BB monoclonal antibodies possess strong antitumor properties, which in turn are the result of their powerful CD8+ T-cell activating, IFN-gamma producing, and cytolytic marker-inducing capabilities. In addition, combination therapy of anti-4-1BB with other anticancer agents, such as radiation, has robust tumor-regressing abilities against nonimmunogenic or poorly immunogenic tumors. Furthermore, the adoptive transfer of ex vivo anti-4-1-BB-activated CD8+ T cells from previously tumor-treated animals efficiently inhibits progression of tumors in recipient mice that have been inoculated with fresh tumors. In addition, targeting of tumors with variants of 4-1BBL directed against 4-1BB also have potent antitumor effects. Currently, a humanized anti-4-1BB is in clinical trials in patients with solid tumors, including melanoma, renal carcinoma, and ovarian cancer, and so far seems to have a favorable toxicity profile. In this review, we discuss the basis of the therapeutic potential of targeting the 4-1BB-4-1BBL pathway in cancer treatment. Mol Cancer Ther; 11(5); 1062-70. (C) 2012 AACR.
引用
收藏
页码:1062 / 1070
页数:9
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