通过基因淘汰/淘汰策略改善对恶性瘤的CAR T细胞疗法:系统性审查
Amirali Karimi1, Sayedeh-Zahra Kazemi-Harikandei1, Sanam Alilou1
1School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Cancer cell international
|December 7, 2025
概括
在CAR T细胞中的基因编辑通过提高疗效和减少副作用来增强癌症治疗. 这一系统性审查确定了105个基因标,以提高CAR T细胞治疗结果.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 生物技术是生物技术.
背景情况:
- 化学抗原受体 (CAR) T细胞疗法在治疗血液和固体瘤方面面临着挑战.
- 基因编辑技术提供了潜在的改进,但缺乏对临床前和临床结果的全面审查.
研究的目的:
- 系统地审查基因编辑CAR T细胞的结果的临床前和临床研究.
- 识别可以被淘汰或被淘汰的基因 (KO/KD),以增强CAR T细胞治疗.
主要方法:
- 按照PRISMA 2020指南进行系统审查,并注册在PROSPERO (ID CRD42022320541) 上.
- 搜索了五个数据库 (PubMed,EMBASE,Cochrane图书馆,科学网,Clinicaltrials.gov) 搜索了关于CAR T细胞和KO/KD基因的研究.
- 包括241个记录 (193个动物,52个人类) 报告了105种蛋白质的KO/KD.
主要成果:
- 对105种蛋白质的基因编辑证明了五个关键的好处:使异性CAR产生,同时限制GVHD,增加CAR T细胞的疗效,减少副作用,限制CAR T细胞兄弟杀伤,并允许并发疗法.
- 人类研究表明,与血液恶性瘤相比,固体瘤的良好结果较少.
结论:
- 本综述强调了各种机制,以提高CAR T细胞治疗的有效性.
- 确定了105个候选基因用于未来的研究,并强调需要更多地关注固体瘤.
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