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:Revolutionizing Cancer Treatments through Stem Cell-Derived CAR T Cells for Immunotherapy: Opening New Horizons for the Future of Oncology.
Revolutionizing Cancer Treatments through Stem Cell-Derived CAR T Cells for Immunotherapy: Opening New Horizons for the Future of Oncology.
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近年来,细胞疗法的进展为多种癌症和自身免疫性疾病的创新治疗铺平了道路。诱导多能干细胞(iPSCs)代表了一项显著的突破,为生成患者特异性细胞类型以用于个性化及异体治疗提供了可能。本综述探讨了iPSC来源的嵌合抗原受体(CAR)T细胞的应用,这是异体癌症免疫治疗中的一种前沿方法。CAR-T 细胞是经过基因工程改造的免疫细胞,旨在靶向特定的肿瘤抗原,其与iPSC技术的整合为增强细胞疗法的疗效、安全性和可扩展性带来了巨大希望。本综述首先阐明了iPSC生成及分化为T细胞的原理,强调了iPSC在提供均一、永不枯竭的CAR-T 细胞来源方面的优势。
此外,我们讨论了通过对iPSC来源的T细胞进行基因修饰以表达各种CAR,强调了这在为多种恶性肿瘤设计定制疗法方面所提供的精确性和灵活性。
值得注意的是,与常规来源的对应细胞相比,iPSC来源的CAR-T 细胞表现出更优越的增殖能力、持久性和抗肿瘤活性,为常规CAR-T 细胞疗法相关的挑战提供了潜在的解决方案。
总之,iPSC来源的CAR-T 细胞代表了细胞疗法的一项突破性进展,在革新免疫治疗格局方面展现出无与伦比的潜力。随着这项技术的不断发展,它有望为与癌症和其他免疫相关疾病作斗争的患者提供更安全、更有效且更广泛可及的治疗选择。本综述旨在阐明iPSC来源CAR-T 细胞的变革潜力,并激发这一动态领域的进一步研究与开发。
Recent advances in cellular therapies have paved the way for innovative treatments of various cancers and autoimmune disorders. Induced pluripotent stem cells (iPSCs) represent a remarkable breakthrough, offering the potential to generate patient-specific cell types for personalized as well as allogeneic therapies. This review explores the application of iPSC-derived chimeric antigen receptor (CAR) T cells, a cutting-edge approach in allogeneic cancer immunotherapies.
CAR T cells are genetically engineered immune cells designed to target specific tumor antigens, and their integration with iPSC technology holds immense promise for enhancing the efficacy, safety, and scalability of cellular therapies. This review begins by elucidating the principles behind iPSC generation and differentiation into T cells, highlighting the advantage of iPSCs in providing a uniform, inexhaustible source of CAR T cells.
Additionally, we discuss the genetic modification of iPSC-derived T cells to express various CARs, emphasizing the precision and flexibility this affords in designing customized therapies for a diverse range of malignancies.
Notably, iPSC-derived CAR T cells demonstrate a superior proliferative capacity, persistence, and anti-tumor activity compared to their conventionally derived counterparts, offering a potential solution to challenges associated with conventional CAR T cell therapies.
In conclusion, iPSC-derived CAR T cells represent a groundbreaking advancement in cellular therapies, demonstrating unparalleled potential in revolutionizing the landscape of immunotherapies. As this technology continues to evolve, it holds the promise of providing safer, more effective, and widely accessible treatment options for patients battling cancer and other immune-related disorders. This review aims to shed light on the transformative potential of iPSC-derived CAR T cells and inspire further research and development in this dynamic field.
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