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用"基因剪刀"剪断癌症枷锁:活体药物TIL细胞瘤疗法首次实现长生存 ...
随着CRISPR 基因编辑技术的诞生,让人类拥有了“魔法剪刀”,为癌症治疗带来革命性可能。作为新型细胞内免疫检查点,CISH 因位于细胞内部,无法被传统免疫疗法的抗体靶向,研究发现,CISH 基因缺失可重新激活免疫系统的抗肿瘤信号。
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