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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Development of chimeric antigen receptor T cells targeting cancer-expressing podocalyxin.
Development of chimeric antigen receptor T cells targeting cancer-expressing podocalyxin.
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。
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。
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.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。