Mo Xuan, Shen Anping, Han Yicun, Xu Li, Miao Jiaqian, Xu Danni, Ji Qing, Cao Yuelong, Ge Guangbo, Zhu Xinyuan, Deng Hongping
Shanghai Frontiers Science Center of TCM Chemical Biology, Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Shi's Center of Orthopedics and Traumatology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
ACS Nano. 2025 Apr 8;19(13):12920-12936. doi: 10.1021/acsnano.4c16671. Epub 2025 Mar 28.
Macrophage plays critical roles in immune-related diseases, acting as a crucial therapeutic target for immunotherapy. Rational design and development of effective therapeutics for macrophage reprogramming are still challenging. Here, we rationally engineered polysaccharide nanoadjuvants to reprogram macrophage functions for enhanced immunotherapy in multiple diseases through a macrophage phenotype-specific nanoprobe (MPSNPr)-assisted high-throughput phenotypic screen. This MPSNPr exhibited high macrophage M1 phenotype specificity because of the formation of H-aggregates on the outer surface and the binding to glucose transporter 1 receptors by the polysaccharide nanocarrier. Based on this MPSNPr, a high-throughput platform was constructed and employed to screen a variety of pharmaceuticals for macrophage reprogramming, being able to identify both pro-inflammatory and anti-inflammatory drug candidates. Polysaccharide nanoadjuvants, Dex-BA and Dex-SAL, were rationally engineered with two potent candidates to amplify macrophage reprogramming efficacy both in vitro and in vivo. Dex-BA significantly inhibited tumor growth by inducing macrophage M1 polarization, dendritic cell maturation, and cytotoxic T cell activation in a mice melanoma model. Dex-SAL alleviated rheumatoid arthritis symptoms with reduced inflammation by reprogramming activated macrophages toward anti-inflammatory phenotype. Our work provides a robust strategy for the rational design and development of effective therapeutics for enhanced macrophage-mediated immunotherapy in diverse diseases.
巨噬细胞在免疫相关疾病中发挥着关键作用,是免疫治疗的重要靶点。合理设计和开发用于巨噬细胞重编程的有效疗法仍然具有挑战性。在此,我们通过巨噬细胞表型特异性纳米探针(MPSNPr)辅助的高通量表型筛选,合理设计工程化多糖纳米佐剂,以重编程巨噬细胞功能,增强多种疾病的免疫治疗效果。由于多糖纳米载体在外表面形成H-聚集体并与葡萄糖转运蛋白1受体结合,该MPSNPr表现出对巨噬细胞M1表型的高度特异性。基于此MPSNPr,构建了一个高通量平台,用于筛选多种用于巨噬细胞重编程的药物,能够识别促炎和抗炎药物候选物。用两种有效候选物合理设计工程化多糖纳米佐剂Dex-BA和Dex-SAL,以在体外和体内放大巨噬细胞重编程效果。在小鼠黑色素瘤模型中,Dex-BA通过诱导巨噬细胞M1极化、树突状细胞成熟和细胞毒性T细胞活化,显著抑制肿瘤生长。Dex-SAL通过将活化的巨噬细胞重编程为抗炎表型,减轻类风湿性关节炎症状并减轻炎症。我们的工作为合理设计和开发有效的疗法提供了强有力的策略,以增强巨噬细胞介导的针对多种疾病的免疫治疗。