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:Exploring CAR-macrophages in non-tumor diseases: Therapeutic potential beyond cancer.
Exploring CAR-macrophages in non-tumor diseases: Therapeutic potential beyond cancer.
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背景:肿瘤治疗取得重大进展后,基于嵌合抗原受体(CAR)的个体化细胞疗法有望改变多种疾病的管理方式。首个获批CAR细胞疗法产品CAR-T 已显示治疗感染性疾病、自身免疫病和纤维化的潜力。CAR巨噬细胞(CAR-M)正成为CAR免疫细胞疗法中有前景的方法,特别是在实体瘤治疗方面,凸显利用巨噬细胞清除病原体和异常细胞的可行性。 综述目的:本文总结CAR-M治疗非肿瘤性疾病的进展,讨论多种CAR胞内激活结构域设计,以及通过调节组织微环境细胞组分与CAR-M之间的相互作用来优化疗效的潜力。此外,本文比较CAR-M疗法与传统药物及CAR-T/NK疗法的特点和优势,并讨论CAR-M临床转化的挑战与前景。 综述的关键科学概念:本文全面阐述CAR-M治疗非肿瘤性疾病,分析其疗法优势和特点,并强调CAR胞内结构域设计对治疗效果的重要影响。此外,文章还讨论开发CAR-M作为新型细胞疗法所面临的挑战及临床转化前景。
BACKGROUND: After significant advancements in tumor treatment, personalized cell therapy based on chimeric antigen receptors (CAR) holds promise for transforming the management of various diseases. CAR-T therapy, the first approved CAR cell therapy product, has demonstrated therapeutic potential in treating infectious diseases, autoimmune disorders, and fibrosis. CAR-macrophages (CAR-Ms) are emerging as a promising approach in CAR immune cell therapy, particularly for solid tumor treatment, highlighting the feasibility of using macrophages to eliminate pathogens and abnormal cells. AIM OF REVIEW: This review summarizes the progress of CAR-M therapy in non-tumor diseases and discusses various CAR intracellular activation domain designs and their potential to optimize therapeutic effects by modulating interactions between cellular components in the tissue microenvironment and CAR-M. Additionally, we discuss the characteristics and advantages of CAR-M therapy compared to traditional medicine and CAR-T/NK therapy, as well as the challenges and prospects for the clinical translation of CAR-M. KEY SCIENTIFIC CONCEPTS OF REVIEW: This review provides a comprehensive understanding of CAR-M for the treatment of non-tumor diseases, analyzes the advantages and characteristics of CAR-M therapy, and highlights the important impact of CAR intracellular domain design on therapeutic efficacy. In addition, the challenges and clinical translation prospects of developing CAR-M as a new cell therapy are discussed.
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