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:Innovative strategies for improving CAR-T cell therapy: A nanomedicine perspective.
Innovative strategies for improving CAR-T cell therapy: A nanomedicine perspective.
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CAR-T(CAR-T)细胞重塑了血液系统恶性肿瘤的治疗格局,为患者提供了一种潜在治愈性选择。尽管免疫肿瘤学领域取得了这些重大里程碑,但CAR-T 细胞日益积累的经验也凸显了该策略的若干局限性。CAR-T 细胞的生产过程复杂、耗时且昂贵,导致药物可及性差。病毒转染系统的潜在致癌风险仍存在争议。治疗相关副作用,如细胞因子释放综合征,可能危及生命。而最大的挑战是与CAR-T 细胞在肿瘤组织中浸润和滞留不良以及免疫抑制性肿瘤微环境(TME)导致的T细胞活化受损相关的疗效不足。迫切需要创新策略来解决这些问题,而纳米医学为这些挑战提供了良好的解决方案。在本综述中,我们全面总结了纳米材料应用于增强CAR-T 细胞治疗的最新进展。
我们审视了创新性基于纳米颗粒的递送系统在CAR-T 细胞生产中的作用,特别关注聚合物递送系统和脂质纳米颗粒(LNPs)。
此外,我们探讨了递送免疫刺激物的各种策略,这些策略通过调节T细胞活力和功能或通过重编程免疫抑制性TME来显著增强CAR-T 细胞的疗效。
另外,我们讨论了若干旨在减轻CAR-T 治疗相关不良反应的新型治疗方法。最后,我们对CAR-T 治疗面临的未来挑战和机遇提供了综合视角。
Chimeric antigen receptor T (CAR-T) cells have reshaped the treatment landscape of hematological malignancies, offering a potentially curative option for patients. Despite these major milestones in the field of immuno-oncology, growing experience with CAR-T cells has also highlighted several limitations of this strategy. The production process of CAR-T cells is complex, time-consuming, and costly, thus leading to poor drug accessibility. The potential carcinogenic risk of viral transfection systems remains a matter of controversy.
Treatment-related side effects, such as cytokine release syndrome, can be life-threatening. And the biggest challenge is the inadequate efficacy related to poor infiltration and retention of CAR-T cells in tumor tissues and impaired T cell activation caused by the immunosuppressive tumor microenvironment (TME).
Innovative strategies are urgently needed to address these problems, and nanomedicine offers good solutions to these challenges. In this review, we provide a comprehensive summary of recent advancements in the application of nanomaterials to enhance CAR-T cell therapy.
We examine the role of innovative nanoparticle-based delivery systems in the production of CAR-T cells, with a particular focus on polymeric delivery systems and lipid nanoparticles (LNPs).
Furthermore, we explore various strategies for delivering immune stimulators, which significantly enhance the efficacy of CAR-T cells by modulating T cell viability and functionality or by reprogramming the immunosuppressive TME.
In addition, we discuss several novel therapeutic approaches aimed at mitigating the adverse effects associated with CAR-T therapies.
Finally, we offer an integrated perspective on the future challenges and opportunities facing CAR-T therapies.
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