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:Recent advancements and persisting challenges in the evolution of next generation car t cell therapy for solid malignancies: a comprehensive review.
Recent advancements and persisting challenges in the evolution of next generation car t cell therapy for solid malignancies: a comprehensive review.
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嵌合抗原受体(CAR)T细胞疗法是治疗癌症最有前景的免疫疗法之一。与仅在主要组织相容性复合体(MHC)呈递抗原时才识别抗原的传统T细胞不同,CAR利用源自抗体的结合结构域直接识别天然的肿瘤相关表面抗原,从而实现不依赖MHC的靶点识别。CAR-T 细胞使用的两种主要细胞毒性机制是:快速释放含有颗粒酶和穿孔素的裂解性颗粒,导致靶细胞凋亡;以及激活死亡受体通路(FasL/Fas或TRAIL),导致半胱天冬酶依赖性细胞死亡。为提高治疗效果,已设计出四代CAR,更先进的第五代正在开发中。
Chimeric antigen receptor (CAR) T-cell therapy is one of the most promising types of immunotherapies for the treatment of cancer. Unlike conventional T cells, which recognize antigens only when presented by the major histocompatibility complex (MHC), CARs use an antibody-derived binding domain to recognize native tumor-associated surface antigens directly, enabling MHC-independent target recognition. The two main cytotoxic mechanisms used by CAR T cells are the quick release of lytic granules containing granzymes and perforin to cause target cell apoptosis and the activation of death-receptor pathways (FasL/Fas or TRAIL) to cause caspase-dependent cell death. Four generations of CAR designs have been created to improve therapeutic efficacy and an advanced fifth generation is under development. Although CAR-T therapies have been very successful in treating hematological malignancies, their efficacy in solid tumors is limited because of immunosuppressive tumor microenvironments, tissue architecture, and antigen expression patterns that prevent CAR-T cell infiltration, activation, and persistence.
With encouraging but early results, CAR T-cell therapy is moving forward into many clinical studies aimed at different solid tumors. Antigens including epidermal growth factor receptor (EGFR), mesothelin (MSLN), Disialoganglioside 2 (GD2), and B7-H3 were the subject of important clinical research conducted between 2021 and 2025. Emerging cellular treatments such as Chimeric Antigen Receptor Natural Killer cells (CAR-NK), CAR-macrophages and T-cell receptor (TCR)-engineered T cells offer alternate options to circumvent the limitations of CAR T-cells in solid tumors.
This review aims to examine the evolution of next-generation CAR-T cell therapy for solid tumors by highlighting recent innovations, key clinical advancements, and persisting therapeutic challenges. It further seeks to analyze the biological and translational barriers limiting efficacy in solid malignancies and to explore emerging strategies and future directions that may enhance clinical outcomes.
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