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:Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy.
Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy.
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嵌合抗原受体(CAR)-T细胞疗法是一种前景广阔的免疫疗法,在过去几十年中取得了显著进展。它涉及对T细胞进行基因修饰,使其靶向表达特定抗原的癌细胞,为治疗多种类型的癌症提供了新方法。
然而,第一代CAR-T 细胞的初期成功因增殖不足和不良结局而受到限制。尽管如此,CAR-T 细胞工程已取得重大进展,推动了最新第五代CAR-T 细胞的发展,其能够靶向多种抗原并克服各自的局限性。尽管有这些进展,一些不足仍阻碍了CAR-T 疗法的广泛应用,包括危及生命的毒性、T细胞耗竭以及实体瘤浸润不足。研究人员已作出大量努力,通过开发改善CAR-T 细胞功能和降低毒性的新策略来解决这些问题。本综述概述了CAR-T 细胞的发展历程,并重点介绍了其结构和制造工艺方面的一些突出进展,包括改善抗原识别、增强T细胞活化和持久性以及克服免疫逃逸的策略。
最后,本综述简要涉及用于癌症治疗的其他免疫细胞,并以讨论CAR-T 在治疗多种疾病(而不仅仅是血液系统肿瘤)中的广阔前景以及CAR-T 细胞疗法广泛临床应用所需解决的挑战作为结尾。
Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of cancer.
However, the initial success of first-generation CAR-T cells was limited due to inadequate proliferation and undesirable outcomes. Nonetheless, significant progress has been made in CAR-T cell engineering, leading to the development of the latest fifth-generation CAR-T cells that can target multiple antigens and overcome individual limitations. Despite these advancements, some shortcomings prevent the widespread use of CAR-T therapy, including life-threatening toxicities, T-cell exhaustion, and inadequate infiltration for solid tumors.
Researchers have made considerable efforts to address these issues by developing new strategies for improving CAR-T cell function and reducing toxicities. This review provides an overview of the path of CAR-T cell development and highlights some of the prominent advances in its structure and manufacturing process, which include the strategies to improve antigen recognition, enhance T-cell activation and persistence, and overcome immune escape.
Finally, the review briefly covers other immune cells for cancer therapy and ends with the discussion on the broad prospects of CAR-T in the treatment of various diseases, not just hematological tumors, and the challenges that need to be addressed for the widespread clinical application of CAR-T cell therapies.
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