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:Facts and Hopes for Neoantigen-Enriched TIL.
Facts and Hopes for Neoantigen-Enriched TIL.
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经过数十年的发展,TIL(肿瘤浸润淋巴细胞)过继转移疗法(即TIL免疫疗法)于2024年获美国FDA批准,用于免疫检查点抑制剂耐药的转移性黑色素瘤患者。将该策略推广至更常见的上皮癌,依赖于转化黑色素瘤患者研究中有关肿瘤与T细胞相互作用的关键发现。其中核心工作是识别新抗原和新抗原反应性TIL。利用实验室技术指导TIL筛选已能介导一定程度的肿瘤消退,但目前仍在开发新的TIL富集策略,以期提高其治疗实体瘤的临床疗效。
After decades of development, adoptive transfer of tumor-infiltrating lymphocytes (TIL) or TIL immunotherapy was approved by the U. S. FDA for patients with checkpoint-refractory metastatic melanoma in 2024. Application of the strategy to more common epithelial cancers has depended on the translation of key findings about tumor and T-cell interactions derived from studies of patients with melanoma.
Central to that effort has been the identification of neoantigens and neoantigen-reactive TIL. Using laboratory techniques to guide the selection of TIL has mediated modest tumor regression, but new strategies to enrich TIL remain in development in the hopes of improving clinical efficacy in the treatment of solid tumors.
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