Department of Biological Systems Engineering, Virginia Tech, Blacksburg, VA 24061, USA; State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, Jiangsu 211816, China.
Department of Biological Systems Engineering, Virginia Tech, Blacksburg, VA 24061, USA.
Acta Biomater. 2023 Aug;166:1-13. doi: 10.1016/j.actbio.2023.04.043. Epub 2023 May 2.
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.
嵌合抗原受体 T (CAR-T) 细胞在治疗血液恶性肿瘤方面取得了突破性疗效,但在实体瘤中的疗效不尽人意,限制了其应用。高昂的价格进一步限制了它们被更广泛人群所获得。因此,迫切需要新的策略来应对这些挑战,而工程生物材料可能是一种很有前途的方法。CAR-T 细胞的制造过程涉及多个步骤,生物材料可以帮助简化或改进其中的几个步骤。在这篇综述中,我们介绍了用于制造或刺激 CAR-T 细胞的工程生物材料的最新进展。我们重点介绍了用于体外或体内转导 CAR 进入 T 细胞的非病毒基因传递纳米颗粒的工程设计。我们还深入探讨了用于局部递送或刺激 CAR-T 细胞的纳米/微米颗粒或可植入支架的工程设计。这些基于生物材料的策略可能会改变 CAR-T 细胞的制造方式,显著降低其成本。利用生物材料调节肿瘤微环境也可以显著提高 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,并讨论了未来的挑战和机遇。
嵌合抗原受体 T (CAR-T) 细胞疗法通过基因工程肿瘤识别技术彻底改变了癌症免疫疗法领域。它们在治疗许多其他疾病方面也很有前途。然而,由于制造成本高,CAR-T 细胞疗法的广泛应用受到了阻碍。CAR-T 细胞很难穿透固体组织,这进一步限制了它们的应用。虽然已经探索了生物策略来改善 CAR-T 细胞疗法,例如确定新的癌症靶点或整合智能 CAR,但生物材料工程为更好的 CAR-T 细胞提供了替代策略。在这篇综述中,我们总结了用于改善 CAR-T 细胞的工程生物材料的最新进展。已经开发了从纳米、微米和宏观尺度的生物材料,以协助 CAR-T 细胞的制造和配方。