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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Elevating the potential of CAR-T cell therapy in solid tumors: exploiting biomaterials-based delivery techniques.
Elevating the potential of CAR-T cell therapy in solid tumors: exploiting biomaterials-based delivery techniques.
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嵌合抗原受体(CAR)T细胞在解决血液系统恶性肿瘤方面展现出令人鼓舞的进展。然而,针对实体瘤的CAR-T 治疗仍然受限,目前尚无FDA批准的CAR-T 产品可供临床使用。主要原因包括浸润不足、积聚不足、肿瘤微环境免疫抑制以及相关副作用。单独使用CAR-T 无法有效克服这些不利障碍。实现更好CAR-T 治疗效果的一条可能有效途径是结合基于生物材料技术的优势。本文总结了在肿瘤部位突破CAR-T 细胞治疗这些障碍的综合生物材料策略,涵盖以下方面:1)生成原位CAR-T 细胞;2)促进CAR-T 细胞运输;3)刺激CAR-T 细胞扩增和浸润;4)改善CAR-T 细胞活性和持久性;5)重编程免疫抑制微环境。此外,还深入讨论了该领域发展的未来需求,特别强调促进创新和推动临床转化。
Chimeric antigen receptor (CAR) T cells exhibit promising progress in addressing hematologic malignancies.
However, CAR-T therapy for solid tumors remains limited, with no FDA-approved CAR-T products available for clinical use at present. Primary reasons include insufficient infiltration, accumulation, tumor immunosuppression of the microenvironment, and related side effects. Single utilization of CAR-T cannot effectively overcome these unfavorable obstacles. A probable effective pathway to achieve a better CAR-T therapy effect would be to combine the benefits of biomaterials-based technology.
In this article, comprehensive biomaterials strategies to break through these obstacles of CAR-T cell therapy at the tumor sites are summarized, encompassing the following aspects: 1) generating orthotopic CAR-T cells; 2) facilitating CAR-T cell trafficking; 3) stimulating CAR-T cell expansion and infiltration; 4) improving CAR-T cell activity and persistence; 5) reprogramming the immunosuppressive microenvironments.
Additionally, future requirements for the development of this field, with a specific emphasis on promoting innovation and facilitating clinical translation, are thoroughly discussed.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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