决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Advancements in targeting CD30 for lymphoma therapy: a historical perspective and future directions.
CD30已成为淋巴瘤诊断、预后和治疗策略的关键标志物。靶向CD30的抗体药物偶联物brentuximab vedotin(BV)(Adcetris)的引入,显著推进了多种淋巴瘤类型的治疗格局,在CD30+淋巴瘤患者中展现出增强的疗效和可控的安全性特征。然而,在少数患者中观察到耐药性。与此同时,针对CD30的创新治疗策略,如CAR-T 细胞疗法和双特异性抗体,正在开发中。这凸显了旨在改善CD30+淋巴瘤患者管理的持续而有力的研究努力。
CD30是肿瘤坏死因子受体超家族的跨膜蛋白。它表达于一小部分活化的T和B淋巴细胞,以及多种淋巴系统肿瘤,包括经典型霍奇金淋巴瘤和许多非霍奇金淋巴瘤,涵盖儿童和成人人群。涵盖领域:本综述深入探讨CD30作为多种淋巴瘤治疗靶点和预后指标的意义。它全面概述了迄今为止开发的抗CD30治疗干预措施,为淋巴瘤治疗研究的未来方向提供见解。文献检索于1987年1月至2024年12月期间使用PubMed、Scopus和Web of Science数据库进行,以识别相关研究。
INTRODUCTION: CD30 is a transmembrane protein of the tumor necrosis factor receptor superfamily. It is expressed on a small subset of activated T and B lymphocytes, and various lymphoid neoplasms, including classical Hodgkin lymphoma and many non-Hodgkin lymphomas in both pediatric and adult populations. AREAS COVERED: This review delves into the significance of CD30 as a therapeutic target and a prognostic indicator for various lymphomas. It provides a comprehensive overview of anti-CD30 therapeutic interventions developed to date, offering insights into the future direction of lymphoma treatment research. Literature search was conducted from January 1987 to December 2024 using PubMed, Scopus, and Web of Science databases to identify relevant studies. EXPERT OPINION: CD30 has emerged as a critical marker of diagnosis, prognosis, and therapeutic strategies of lymphomas. The introduction of brentuximab vedotin (BV) (Adcetris), an antibody-drug conjugate targeting CD30, has significantly advanced the treatment landscape for multiple lymphoma types, demonstrating enhanced efficacy and manageable safety profiles in CD30+ lymphomas patients. However, drug resistance is observed in few patients. Concurrently, innovative therapeutic strategies targeting CD30, such as chimeric antigen receptor T-cells therapies and bispecific antibodies, are in development. This underscores a strong and ongoing research effort aimed at improving the management of patients with CD30+ lymphomas.
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