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针对4-1BB T细胞活化分子的单克隆抗体可根除已形成的肿瘤。

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

作者信息

Melero I, Shuford W W, Newby S A, Aruffo A, Ledbetter J A, Hellström K E, Mittler R S, Chen L

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, Washington 98121, USA.

出版信息

Nat Med. 1997 Jun;3(6):682-5. doi: 10.1038/nm0697-682.

Abstract

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.

摘要

4-1BB糖蛋白是肿瘤坏死因子受体超家族的成员,可与在多种抗原呈递细胞(如巨噬细胞和活化的B细胞)上表达的高亲和力配体(4-1BBL)结合。4-1BB的表达仅限于致敏的CD4+和CD8+T细胞,通过与4-1BBL结合或抗体连接进行的4-1BB信号传导为T细胞活化和生长传递双重促有丝分裂信号。这些观察结果表明4-1BB在T细胞介导的免疫反应放大中起重要作用。我们现在表明,给予抗4-1BB单克隆抗体可以根除小鼠体内已形成的大肿瘤,包括免疫原性差的Ag104A肉瘤和高致瘤性的P815肥大细胞瘤。抗4-1BB单克隆抗体诱导的免疫反应由CD8+和CD4+T细胞介导,并伴有肿瘤选择性细胞毒性T细胞活性的显著增强。我们的数据表明,类似的方法可能对人类癌症的免疫治疗有效。

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