Monoclonal antibodies against the 4-1BB T-cell activation molecule eradicate established tumors

被引:755
作者
Melero, I [1 ]
Shuford, WW [1 ]
Newby, SA [1 ]
Aruffo, A [1 ]
Ledbetter, JA [1 ]
Hellstrom, KE [1 ]
Mittler, RS [1 ]
Chen, LP [1 ]
机构
[1] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,SEATTLE,WA 98121
关键词
D O I
10.1038/nm0697-682
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
The 4-1BB glycoprotein is a member of the tumor necrosis factor receptor superfamily(1-4) and binds to a high-affinity ligand (4-1BBL) expressed on several antigen-presenting cells such as macrophages and activated B cells(5,6). Expression of 4-1BB is restricted to primed CD4(+) and CD8(+) T cells(7), and 4-1BB signaling either by binding to 4-1BBL or by antibody ligation delivers a dual mitogenic signal for T-cell activation and growth(8-12). These observations suggest an important role for 4-1BB in the amplification of T cell-mediated immune responses. We now show that administration of anti-4-1BB monoclonal antibodies can eradicate established large tumors in mice, including the poorly immunogenic Ag104A sarcoma and the highly tumorigenic P815 masto cytoma. The immune response induced by anti-4-1BB monoclonal antibodies is mediated by both CD8(+) and CD4(+) T cells and is accompanied by a marked augmentation of tumor-selective cytolytic T-cell activity. Our data suggest that a similar approach may be efficacious for immunotherapy of human cancer.
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收藏
页码:682 / 685
页数:4
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