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:Immunotherapy and immunoengineering for breast cancer; a comprehensive insight into CAR-T cell therapy advancements, challenges and prospects.
Immunotherapy and immunoengineering for breast cancer; a comprehensive insight into CAR-T cell therapy advancements, challenges and prospects.
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CAR-T 细胞疗法体现了针对 BC 的先进免疫疗法,但建议进一步开展临床前和临床评估,以实现最大化的疗效和安全性。
乳腺癌(BC)是一种高度流行的实体癌,免疫细胞浸润程度高,使其成为肿瘤特异性免疫治疗的重要候选对象。嵌合抗原受体(CAR)-T细胞正作为免疫治疗工具崭露头角,其通过基因工程改造的受体能够高效识别并攻击表达特定靶抗原的肿瘤细胞。CAR设计的技术进步已提供了五代CAR-T 细胞,适用于广泛的癌症患者,同时提升了CAR-T 细胞治疗的安全性。然而,由于特定抗原的丢失、肿瘤的免疫抑制性质以及CAR-T 细胞诱导的毒性,CAR-T 细胞治疗对乳腺癌效果不佳。下一代CAR-T 细胞能够主动穿越肿瘤血管屏障,长期持续存在并破坏肿瘤微环境(TME)以阻断免疫逃逸。
Breast cancer (BC) is a highly prevalent solid cancer with a high-rise infiltration of immune cells, turning it into a significant candidate for tumor-specific immunotherapies. Chimeric antigen receptor (CAR)-T cells are emerging as immunotherapeutic tools with genetically engineered receptors to efficiently recognize and attack tumor cells that express specific target antigens. Technological advancements in CAR design have provided five generations of CAR-T cells applicable to a wide range of cancer patients while boosting CAR-T cell therapy safety. However, CAR-T cell therapy is ineffective against breast cancer because of the loss of specified antigens, the immunosuppressive nature of the tumor and CAR-T cell-induced toxicities. Next-generation CAR-T cells actively pass through the tumor vascular barriers, persist for extended periods and disrupt the tumor microenvironment (TME) to block immune escape.
CAR-T cell therapy embodies advanced immunotherapy for BC, but further pre-clinical and clinical assessments are recommended to achieve maximized efficiency and safety.
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