CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Current perspectives on resistance to chimeric antigen receptor T-cell therapy and strategies to improve efficacy in B-cell lymphoma.
Current perspectives on resistance to chimeric antigen receptor T-cell therapy and strategies to improve efficacy in B-cell lymphoma.
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CAR-T 治疗化疗难治性B细胞淋巴瘤虽疗效显著,但相当一部分患者无应答或复发,耐药是改善疗效和长期生存的重要障碍。目前临床缺乏可靠方法预先判断患者是否应答。CD19靶抗原丢失仅解释约30%的治疗失败。近期研究揭示,CD19阳性复发还可由肿瘤内在耐药、T细胞质量或制备问题,以及不利肿瘤微环境介导的CAR-T 耗竭造成。本综述总结B细胞淋巴瘤CAR-T 治疗后耐药和复发机制的临床前及临床研究进展,讨论克服耐药的新策略,以及有助于临床医生优化和个体化CAR-T 治疗的发现。
Although chimeric antigen receptor (CAR) T-cell therapy has demonstrated remarkable efficacy in patients with chemo-refractory B-cell lymphoma, a significant portion is refractory or relapse. Resistance is a major barrier to improving treatment efficacy and long-term survival in CAR T-cell therapy, and clinicians have very limited tools to discriminate a priori patients who will or will not respond to treatment.
While CD19-negative relapses due to loss of target antigen is well described, it accounts for only about 30% of cases with treatment failure. Recent efforts have shed light on mechanisms of CD19-positive relapse due to tumor intrinsic resistance, T-cell quality/manufacturing, or CAR T-cell exhaustion mediated by hostile tumor microenvironment.
Here, we review the latest updates of preclinical and clinical trials to investigate the mechanisms of resistance and relapse post CAR T-cell therapy in B cell lymphoma and discuss novel treatment strategies to overcome resistance as well as advances that are useful for a CAR T therapist to optimize and personalize CAR T-cell therapy.
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