抗原提呈细胞
过继性细胞移植
材料科学
免疫疗法
树突状细胞
细胞生物学
T细胞
抗原
纳米技术
化学
免疫学
生物
免疫系统
作者
Ya‐Ling He,Lele Sun,Rui Chen,Zijian Xiong,Wenzhuo Yu,Zhuang Liu,Hong Chen
出处
期刊:Biomaterials
[Elsevier]
日期:2023-05-01
卷期号:296: 122048-122048
被引量:1
标识
DOI:10.1016/j.biomaterials.2023.122048
摘要
A variety of bioactive materials are currently developed to expand T cells ex vivo for adoptive T cell immunotherapy, also known as called artificial antigen-presenting cells (aAPCs). However, almost all the reported designs exhibit relatively smooth surface modified with T cell activating biomolecules, and therefore cannot well mimic the dendritic morphological characteristics of dendritic cells (DCs), the most important type of natural antigen-presenting cells (APCs) with high specific surface areas. Here, we propose a hydrophilic monomer-mediated surface morphology control strategy to synthesize biocompatible dendritic poly(N-isopropylacrylamide) (PNIPAM) microspheres for constructing aAPCs with surface morphology mimicking natural APCs (e.g., DCs). Interestingly, when maintaining the same ligands density, dendritic polymeric microspheres-based aAPCs (DPM beads) can more efficiently expand CD8+ T cells than that with smooth surfaces. Moreover, adoptive transfer of antigen-specific CD8+ T cells expanded by the DPM beads show significant antitumor effect of B16-OVA tumor bearing mice. Therefore, we provide a new concept for constructing biomimetic aAPCs with enhanced T cell expansion ability.
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