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DOI: 10.3791/59949-v
Please note that some of the translations on this page are AI generated. Click here for the English version.
我们描述了一种可靠地生成嵌合抗原受体(CAR)T细胞的方法,并测试其体外和体内的分化和功能。
脱利-at-at功能能力,在输液后,具有促进、增殖和cit-el-uric活性,是有效采用免疫疗法的关键组成部分。例如,在实体肿瘤中,CAR T细胞可以穿透实体肿瘤,并接受最佳的抗原刺激;然而,它们的整体感染和增殖在人体内受到阻碍。这种方法的主要好处是,它可以保留 CAR T 细胞的质量或 CAR T 细胞的分化状态,而无需产生最终分化或耗尽的 T 细胞,这将降低增殖能力或输液后的有效功能差。
这种技术可能很困难,因为T细胞对细胞浓度或培养的血管的表面面积非常敏感。以及他们的代谢需求。从本质上讲,T细胞需要在整个过程中保持快乐,否则它们不会生长。
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