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:Biomaterials for chimeric antigen receptor T cell engineering.
Biomaterials for chimeric antigen receptor T cell engineering.
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CAR-T(CAR-T)细胞在血液系统恶性肿瘤中取得了突破性疗效,但在实体瘤中疗效不佳,限制了其应用。其高昂的价格进一步限制了更广泛人群的可及性。迫切需要新的策略来应对这些挑战,而工程化生物材料可能是一种有前景的方法。已建立的CAR-T 细胞生产流程涉及多个步骤,生物材料可以帮助简化或改进其中若干步骤。在本综述中,我们涵盖用于生产或刺激CAR-T 细胞的工程化生物材料的最新进展。
我们重点关注用于在体外/离体或体内将CAR转导至T细胞的非病毒基因递送纳米颗粒的工程化。我们还深入探讨用于局部递送或刺激CAR-T 细胞的纳米/微粒或可植入支架的工程化。这些基于生物材料的策略可能改变CAR-T 细胞的生产方式,显著降低其成本。用生物材料调控肿瘤微环境也可以显著增强CAR-T 细胞在实体瘤中的疗效。
我们特别关注过去五年取得的进展,并讨论未来挑战和机遇的前景。意义声明:CAR-T(CAR-T)细胞疗法通过基因工程改造的肿瘤识别彻底改变了癌症免疫治疗领域。它们在治疗许多其他疾病方面也很有前景。
然而,CAR-T 细胞疗法的广泛应用受到高生产成本的阻碍。CAR-T 细胞对实体组织渗透性差进一步限制了其使用。尽管已经探索了生物学策略来改进CAR-T 细胞疗法,例如识别新的癌症靶点或整合智能CAR,但生物材料工程为获得更好的CAR-T 细胞提供了替代策略。在这篇综述中,我们总结了用于CAR-T 细胞改进的生物材料工程的最新进展。从纳米、微米到宏观尺度的生物材料已被开发出来,以辅助CAR-T 细胞的生产和制剂。
Chimeric antigen receptor T (CAR-T) cells have achieved breakthrough efficacies against hematological malignancies, but their unsatisfactory efficacies in solid tumors limit their applications. The prohibitively high prices further restrict their access to broader populations.
Novel strategies are urgently needed to address these challenges, and engineering biomaterials can be one promising approach. The established process for manufacturing CAR-T cells involves multiple steps, and biomaterials can help simplify or improve several of them. In this review, we cover recent progress in engineering biomaterials for producing or stimulating CAR-T cells.
We focus on the engineering of non-viral gene delivery nanoparticles for transducing CAR into T cells ex vivo/in vitro or in vivo.
We also dive into the engineering of nano-/microparticles or implantable scaffolds for local delivery or stimulation of CAR-T cells. These biomaterial-based strategies can potentially change the way CAR-T cells are manufactured, significantly reducing their cost. Modulating the tumor microenvironment with the biomaterials can also considerably enhance the efficacy of CAR-T cells in solid tumors.
We pay special attention to progress made in the past five years, and perspectives on future challenges and opportunities are also discussed. STATEMENT OF SIGNIFICANCE: Chimeric antigen receptor T (CAR-T) cell therapies have revolutionized the field of cancer immunotherapy with genetically engineered tumor recognition. They are also promising for treating many other diseases.
However, the widespread application of CAR-T cell therapy has been hampered by the high manufacturing cost. Poor penetration of CAR-T cells into solid tissues further restricted their use. While biological strategies have been explored to improve CAR-T cell therapies, such as identifying new cancer targets or integrating smart CARs, biomaterial engineering provides alternative strategies toward better CAR-T cells.
In this review, we summarize recent advances in engineering biomaterials for CAR-T cell improvement. Biomaterials ranging from nano-, micro-, and macro-scales have been developed to assist CAR-T cell manufacturing and formulation.
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