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抗 CD19 CAR T 细胞能有效地重定向以杀死实体瘤细胞。

Anti-CD19 CAR T cells potently redirected to kill solid tumor cells.

机构信息

Aleta Biotherapeutics, Natick, MA, United States of America.

University of Minnesota, Minneapolis, MN, United States of America.

出版信息

PLoS One. 2021 Mar 18;16(3):e0247701. doi: 10.1371/journal.pone.0247701. eCollection 2021.

Abstract

Successful CAR T cell therapy for the treatment of solid tumors requires exemplary CAR T cell expansion, persistence and fitness, and the ability to target tumor antigens safely. Here we address this constellation of critical attributes for successful cellular therapy by using integrated technologies that simplify development and derisk clinical translation. We have developed a CAR-CD19 T cell that secretes a CD19-anti-Her2 bridging protein. This cell therapy strategy exploits the ability of CD19-targeting CAR T cells to interact with CD19 on normal B cells to drive expansion, persistence and fitness. The secreted bridging protein potently binds to Her2-positive tumor cells, mediating CAR-CD19 T cell cytotoxicity in vitro and in vivo. Because of its short half-life, the secreted bridging protein will selectively accumulate at the site of highest antigen expression, ie. at the tumor. Bridging proteins that bind to multiple different tumor antigens have been created. Therefore, antigen-bridging CAR-CD19 T cells incorporate critical attributes for successful solid tumor cell therapy. This platform can be exploited to attack tumor antigens on any cancer.

摘要

成功的 CAR T 细胞疗法治疗实体瘤需要优秀的 CAR T 细胞扩增、持久性和适应性,以及安全靶向肿瘤抗原的能力。在这里,我们通过使用简化开发和降低临床转化风险的集成技术来解决成功细胞治疗的这一组关键属性。我们开发了一种分泌 CD19-抗 Her2 桥接蛋白的 CAR-CD19 T 细胞。这种细胞治疗策略利用了靶向 CD19 的 CAR T 细胞与正常 B 细胞上的 CD19 相互作用的能力,以驱动扩增、持久性和适应性。分泌的桥接蛋白可与 Her2 阳性肿瘤细胞强力结合,介导 CAR-CD19 T 细胞在体外和体内的细胞毒性。由于其半衰期短,分泌的桥接蛋白将选择性地在抗原表达最高的部位(即肿瘤)积累。已经创建了可与多种不同肿瘤抗原结合的桥接蛋白。因此,抗原桥接的 CAR-CD19 T 细胞包含成功的实体瘤细胞治疗的关键属性。该平台可用于攻击任何癌症上的肿瘤抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03d2/7971483/8c87f6b1f5ae/pone.0247701.g001.jpg

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