Ariail Emily, Garcia Espinoza Nikol, Stephenson A Carson, Spangler Jamie B
Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, USA.
Cell Syst. 2024 Dec 18;15(12):1198-1208. doi: 10.1016/j.cels.2024.11.007.
T cells are key mediators of the adaptive immune response, playing both direct and supporting roles in the destruction of foreign pathogenic threats as well as pathologically transformed host cells. The natural process through which T cells are activated requires coordinated molecular interactions between antigen-presenting cells and T cells. Promising advances in biomaterial design have catalyzed the development of artificial platforms that mimic the natural process of T cell stimulation, both to bolster the performance of cell therapies by activating T cells ex vivo prior to adoptive cell transfer and to directly activate T cells in vivo as off-the-shelf treatments. This review focuses on innovative strategies in T cell-stimulating platform design for applications in cancer therapy. We specifically highlight progress in bead-based artificial antigen-presenting cell engineering, hydrogel-based scaffolds, DNA-based systems, alternative polymeric strategies, and soluble activation approaches. Collectively, these advances are expanding the repertoire of tools for targeted immune activation.
T细胞是适应性免疫反应的关键介质,在破坏外来致病威胁以及病理转化的宿主细胞方面发挥着直接和支持作用。T细胞被激活的自然过程需要抗原呈递细胞和T细胞之间协调的分子相互作用。生物材料设计方面的有前景的进展推动了人工平台的发展,这些平台模仿T细胞刺激的自然过程,既可以通过在过继性细胞转移前体外激活T细胞来增强细胞疗法的性能,也可以作为现成的治疗方法在体内直接激活T细胞。本综述重点关注用于癌症治疗的T细胞刺激平台设计的创新策略。我们特别强调基于珠子的人工抗原呈递细胞工程、基于水凝胶的支架、基于DNA的系统、替代聚合物策略和可溶性激活方法方面的进展。总的来说,这些进展正在扩大靶向免疫激活工具的范围。