嵌合抗原受体
细胞因子释放综合征
CD19
医学
白血病
免疫学
耐火材料(行星科学)
抗原
癌症研究
细胞疗法
B细胞
T细胞
肿瘤科
细胞
抗体
生物
免疫系统
天体生物学
遗传学
作者
Luna Acharya,Alpana Garg,P Manoj,Rupesh Kshetri,Udhayvir Singh Grewal,Prajwal Dhakal
出处
期刊:Journal of Investigative Medicine
[BMJ]
日期:2023-12-01
卷期号:72 (1): 32-46
标识
DOI:10.1177/10815589231191811
摘要
Acute lymphoblastic leukemia (ALL) is the second most common acute leukemia in adults with a poor prognosis with relapsed or refractory (R/R) B-cell lineage ALL (B-ALL). Anti-CD19 chimeric antigen receptor (CAR) T-cell therapy has shown excellent response rates in RR B-ALL, but most patients relapse due to poor persistence of CAR T-cell therapy or other tumor-associated escape mechanisms. In addition, anti-CD19 CAR T-cell therapy causes several serious side effects such as cytokine release syndrome and neurotoxicity. In this review, we will discuss novel CAR targets, CAR constructs, and various strategies to boost CARs for the treatment of RR B-ALL. In addition, we discuss a few novel strategies developed to reduce the side effects of CAR.
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