当前位置:
X-MOL 学术
›
Clin. Cancer Res.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Targeting T-cell costimulation to the surface of tumor cells
Clinical Cancer Research ( IF 10.0 ) Pub Date : 2024-11-12 , DOI: 10.1158/1078-0432.ccr-24-3003 Iñaki Eguren-Santamaría, Miguel F. Sanmamed, Paula Molero-Glez, Jose Luis Perez-Gracia, Ignacio Melero
Clinical Cancer Research ( IF 10.0 ) Pub Date : 2024-11-12 , DOI: 10.1158/1078-0432.ccr-24-3003 Iñaki Eguren-Santamaría, Miguel F. Sanmamed, Paula Molero-Glez, Jose Luis Perez-Gracia, Ignacio Melero
Bispecific agents targeting tumor-cell surface antigens and activating receptors on T lymphocytes are being developed for solid tumors. Effective and safe strategies depend on target specificity and at least relative tumor-tissue confinement of T-cell activation. Novel evidence suggests that constructs targeting HER2 on tumor cells with the aim of providing costimulation (signal-2) to T lymphocytes via CD137 (4-1BB) are safe and can meaningfully invigorate antitumor responses in a proportion of patients.
中文翻译:
将 T 细胞共刺激靶向肿瘤细胞表面
针对实体瘤的靶向肿瘤细胞表面抗原和 T 淋巴细胞激活受体的双特异性药物正在开发中。有效和安全的策略取决于靶标特异性和至少 T 细胞活化的相对肿瘤组织限制。新的证据表明,靶向肿瘤细胞上的 HER2 的构建体旨在通过 CD137 (4-1BB) 向 T 淋巴细胞提供共刺激(信号-2)是安全的,并且可以有意义地激发一部分患者的抗肿瘤反应。
更新日期:2024-11-12
中文翻译:
将 T 细胞共刺激靶向肿瘤细胞表面
针对实体瘤的靶向肿瘤细胞表面抗原和 T 淋巴细胞激活受体的双特异性药物正在开发中。有效和安全的策略取决于靶标特异性和至少 T 细胞活化的相对肿瘤组织限制。新的证据表明,靶向肿瘤细胞上的 HER2 的构建体旨在通过 CD137 (4-1BB) 向 T 淋巴细胞提供共刺激(信号-2)是安全的,并且可以有意义地激发一部分患者的抗肿瘤反应。