单克隆抗体
T细胞
生物
CD8型
免疫系统
抗原
免疫疗法
细胞毒性T细胞
细胞溶解
癌症研究
抗体
癌症免疫疗法
肿瘤坏死因子α
免疫学
分子生物学
生物化学
体外
作者
Ignacio Melero,Walter W. Shuford,S A Newby,Alejandro Aruffo,Jeffrey A. Ledbetter,Karl Erik Hellström,Robert S. Mittler,Lieping Chen
出处
期刊:Nature Medicine
[Springer Nature]
日期:1997-06-01
卷期号:3 (6): 682-685
被引量:880
摘要
The 4-1BB glycoprotein is a member of the tumor necrosis factor receptor superfamily and binds to a high-affinity ligand (4-1BBL) expressed on several antigen-presenting cells such as macrophages and activated B cells. Expression of 4-1BB is restricted to primed CD4+ and CD8+ T cells, 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. 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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