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:Cell-based cancer immunotherapy: milestones, mechanistic insights, and emerging therapeutic directions.
Cell-based cancer immunotherapy: milestones, mechanistic insights, and emerging therapeutic directions.
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。
细胞免疫疗法已成为现代癌症治疗中的变革性方式,可补充手术、化疗、放疗和分子靶向治疗等传统手段。本综述整合并更新快速演进的细胞免疫治疗领域,涵盖嵌合抗原受体(CAR)T 细胞、T 细胞受体(TCR)工程化 T 细胞、TIL(肿瘤浸润淋巴细胞)、树突状细胞(DC)疫苗、自然杀伤(NK)细胞疗法和巨噬细胞靶向策略。文章阐明各治疗形式的作用机制,概述其在血液系统恶性肿瘤和实体瘤中的临床结局,并结合治疗相关毒性、耐药机制及持久应答障碍,批判性评估治疗表现。此外,综述重点介绍旨在减少抗原逃逸、克服免疫抑制性肿瘤微环境,以及解决生产、规模化和可及性问题的新一代策略。总体而言,这些进展确立了细胞免疫疗法作为精准肿瘤学核心组成部分的地位,并使其有望在多种癌症类型中带来持久且更广泛可及的临床获益。
Cell-based immunotherapies have emerged as a transformative modality in modern cancer treatment, complementing conventional approaches such as surgery, chemotherapy, radiotherapy, and molecularly targeted therapies.
This review provides an integrated and up-to-date synthesis of the rapidly evolving landscape of cellular immunotherapy, encompassing chimeric antigen receptor (CAR) T cells, T cell receptor (TCR)-engineered T cells, tumor-infiltrating lymphocytes (TILs), dendritic cell (DC) vaccines, natural killer (NK) cell-based therapies, and macrophage-directed strategies.
We delineate the mechanistic foundations underlying each modality, summarize clinical outcomes across both hematologic malignancies and solid tumors, and critically evaluate therapeutic performance in the context of treatment-associated toxicities, resistance mechanisms, and barriers to durable response.
Furthermore, we highlight emerging next-generation strategies designed to mitigate antigen escape, overcome immunosuppressive tumor microenvironments, and address challenges related to manufacturing, scalability, and accessibility. Collectively, these advances establish cell-based immunotherapies as a central component of precision oncology, with expanding potential to deliver durable and broadly accessible clinical benefit across diverse cancer types.
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