免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Melanoma-Associated Antigen Family A (MAGE-A): A Promising Target for Cancer Immunotherapy?
The Melanoma-Associated Antigen Family A (MAGE-A): A Promising Target for Cancer Immunotherapy?
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
过去十年中,早期识别肿瘤相关抗原的努力为靶向癌症治疗提供了独特的癌症表位。MAGE-A 蛋白是癌/睾丸(CT)抗原的一个亚类,作为免疫豁免位点,由 MHC I 类分子呈递于细胞表面。这是由于它们仅限于生殖细胞和多种癌症中表达,而在这些癌症中,它们与化疗耐药、转移以及生存潜力不断增强的癌细胞相关。这使得它们成为设计有效且特异性免疫治疗的一个有吸引力的候选靶点,从而表明通过癌症疫苗、过继性 T 细胞转移或联合疗法靶向致癌性 MAGE-A 将具有前景。在这篇综述中,我们总结并讨论了针对这些抗原的既往和正在进行的(临床前)临床研究,同时考虑到各种治疗策略的优缺点,以推测 MAGE-A 特异性免疫治疗的未来方向。
Early efforts to identify tumor-associated antigens over the last decade have provided unique cancer epitopes for targeted cancer therapy. MAGE-A proteins are a subclass of cancer/testis (CT) antigens that are presented on the cell surface by MHC class I molecules as an immune-privileged site. This is due to their restricted expression to germline cells and a wide range of cancers, where they are associated with resistance to chemotherapy, metastasis, and cancer cells with an increasing potential for survival.
This makes them an appealing candidate target for designing an effective and specific immunotherapy, thereby suggesting that targeting oncogenic MAGE-As with cancer vaccination, adoptive T-cell transfer, or a combination of therapies would be promising. In this review, we summarize and discuss previous and ongoing (pre-)clinical studies that target these antigens, while bearing in mind the benefits and drawbacks of various therapeutic strategies, in order to speculate on future directions for MAGE-A-specific immunotherapies.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。