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靶向肿瘤表达 podocalyxin 的 CAR-T 细胞的开发

英文原题:Development of chimeric antigen receptor T cells targeting cancer-expressing podocalyxin.

查看英文原题

Development of chimeric antigen receptor T cells targeting cancer-expressing podocalyxin.

PubMed 2025/01/04(内容时间) Regen Ther Q2 · IF 4(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)-T细胞疗法已经彻底改变了CD19阳性B细胞恶性肿瘤的治疗。然而,该领域正在迅速发展以靶向其他抗原,例如podocalyxin(PODXL),这是一种跨膜蛋白,与多种癌症的肿瘤进展和不良预后相关。

本研究探讨了靶向PODXL的CAR-T 细胞的潜力,利用癌症特异性单克隆抗体(CasMab)技术来增强CAR-T 细胞疗法的特异性和安全性。

我们基于源自癌症特异性单克隆抗体PcMab-6的单链可变片段(scFv)开发了CAR-T 细胞,该抗体选择性靶向表达PODXL的癌细胞上的糖基化修饰。作为对照,还从PcMab-47(一种针对PODXL的非癌症特异性抗体)生成了CAR-T 细胞。体外实验表明,与PcMab-47衍生的CAR-T 细胞相比,基于PcMab-6的CAR-T 细胞表现出显著的抗肿瘤活性,同时对正常细胞的脱靶效应降低。

此外,为了增强这些CAR-T 细胞的持久性和治疗效果,我们开发了PcMab-6 scFv的人源化版本。人源化CAR-T 细胞在体内显示出延长的抗肿瘤效果,证明了延长治疗活性的潜力。这些发现强调了CasMab技术在生成用于实体瘤的高度特异性和更安全的CAR-T 细胞疗法中的实用性,突出了人源化CAR-T 细胞在临床应用中的前景。

展开英文摘要原文

Chimeric Antigen Receptor (CAR)-T cell therapy has revolutionized the treatment of CD19-positive B-cell malignancies.

However, the field is rapidly evolving to target other antigens, such as podocalyxin (PODXL), a transmembrane protein implicated in tumor progression and poor prognosis in various cancers.

This study explores the potential of PODXL-targeted CAR-T cells, utilizing a cancer-specific monoclonal antibody (CasMab) technique to enhance the specificity and safety of CAR-T cell therapy.

We developed CAR-T cells based on the single-chain variable fragment (scFv) derived from the cancer-specific monoclonal antibody PcMab-6, which selectively targets glycosylation modifications on PODXL-expressing cancer cells. As a control, CAR-T cells were also generated from PcMab-47, a non-cancer-specific antibody for PODXL. In vitro experiments demonstrated that CAR-T cells based on PcMab-6 exhibited significant antitumor activity with reduced off-target effects on normal cells compared to PcMab-47-derived CAR-T cells.

Additionally, to enhance the persistence and therapeutic efficacy of these CAR-T cells, we developed a humanized version of PcMab-6 scFv. The humanized CAR-T cells showed extended antitumor effects in vivo , demonstrating the potential for prolonged therapeutic activity.

These findings underscore the utility of CasMab technology in generating highly specific and safer CAR-T cell therapies for solid tumors, highlighting the promise of humanized CAR-T cells for clinical application.

论文信息

作者
Mishima Y、Okada S、Ishikawa A、Wang B、Waseda M、Kaneko MK、Kato Y、Kaneko S
单位
Department of Cancer Immunotherapy and Immunology, Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.Japan
期刊
Regenerative therapy2025 Mar
原文标识
PubMed 39867135 · DOI 10.1016/j.reth.2024.12.010