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Current status of genetic modification of T cells for cancer treatment

机译:T细胞基因修饰用于癌症治疗的现状

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摘要

Clinical studies of adoptive immunotherapy with T cells have shown activity directed at hematologic and solid malignancies and viral infections. Genetic modification of infused T cells offers the prospect of improving such therapies and has already been used to track infused T cells, insert suicide genes and redirect the immune response towards specific Ag. Pre-clinical studies are evaluating novel approaches to genetically modify T cells to confer resistance to tumor evasion mechanisms. There is also increasing interest in developing suicide gene strategies as a failsafe mechanism to eradicate genetically modified cells should adverse effects occur.
机译:T细胞过继免疫疗法的临床研究表明,该活性针对血液学和实体恶性肿瘤以及病毒感染。注入的T细胞的基因修饰提供了改善此类疗法的前景,并且已经被用于跟踪注入的T细胞,插入自杀基因并将免疫应答重定向至特定的Ag。临床前研究正在评估对T细胞进行基因修饰以赋予对肿瘤逃逸机制抗性的新方法。开发自杀基因策略作为一种在出现不良反应时根除转基因细胞的故障安全机制也越来越引起人们的兴趣。

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