← 返回

构建新型 CD19/CD22 双靶点 CAR-T 细胞以增强抗肿瘤活性

英文原题:Engineering Novel CD19/CD22 Dual-Target CAR-T Cells for Improved Anti-Tumor Activity.

查看英文原题

Engineering Novel CD19/CD22 Dual-Target CAR-T Cells for Improved Anti-Tumor Activity.

PubMed 2021/11/25(内容时间) Cancer Invest Q3 · IF 2.2(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

尽管B细胞急性淋巴细胞白血病(B-ALL)接受CAR-T 细胞治疗后缓解率很高,但靶抗原丢失导致的复发日益被认为是免疫逃逸的一种机制。我们假设同时靶向CD19和CD22可能改善CAR-T 效果。建立体外和体内白血病模型,观察BiCAR-T、CD19 CAR-T、CD22 CAR-T 和LoopCAR6细胞的抗肿瘤作用。我们发现BiCAR-T 细胞在体外和体内均表现出显著的细胞毒性。CD19/CD22双价CAR为测试同时靶向是否可降低抗原丢失风险提供了机会。

展开英文摘要原文

Despite high remission rates following chimeric antigen receptor T cell (CAR-T) cell therapy in B-cell acute lymphoblastic leukemia (B-ALL), relapse due to loss of the targeted antigen is increasingly recognized as a mechanism of immune escape.

We hypothesized that simultaneous targeting of CD19 and CD22 may improve the CAR-T effect. The in vitro and in vivo leukemia model was established, and the anti-tumor effects of BiCAR-T, CD19 CAR-T, CD22 CAR-T, and LoopCAR6 cells were observed.

We found that the BiCAR-T cells showed significant cytotoxicity in vitro and in vivo . The CD19/CD22 bivalent CAR provides an opportunity to test whether simultaneous targeting may reduce the risk of antigen loss.

论文信息

作者
Zeng W、Zhang Q、Zhu Y、Ou R、Peng L、Wang B、Shen H、Liu Z
第一作者单位
National Center for International Research of Bio-targeting Theranostics, Guangxi Key Laboratory of Bio-targeting Theranostics, Collaborative Innovation Center for Targeting Tumor Diagnosis and Therapy, Guangxi Talent Highland of Bio-targeting Theranostics, Guangxi Medical University, Nanning, China.China
通讯作者单位
Department of Hematology, Guangdong Second Provincial General Hospital, Guangzhou, China.China
期刊
Cancer investigation2022 Mar
原文标识
PubMed 34797742 · DOI 10.1080/07357907.2021.2005798