Xu Xiaoman, Song Yunmei, Li Mingli, Liu Fengxi, Zhang Huiwen, Xu Jingxia, Gao Juwei, Lv Yanna, Zhang Bo, Garg Sanjay
School of Pharmacy, Shandong Second Medical University, Weifang, 261053, Shandong Province, PR China.
School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, South Australia, 5000, Australia.
Mater Today Bio. 2025 Jun 25;33:102012. doi: 10.1016/j.mtbio.2025.102012. eCollection 2025 Aug.
Triple-negative breast cancer (TNBC) remains a clinical challenge due to its aggressive nature. Conventional chemo-immunotherapy suffers from poor tumor targeting and systemic toxicity, necessitating advanced delivery systems for synergistic drug combinations. This study constructed a biomimetic nanodrug delivery system by coating nanomicelles with 4T1 tumor cell membranes. This strategy leverages the homologous targeting ability of tumor cell membranes to improve the accumulation of nanomicelles within TNBC tissues. The cytotoxic agent bortezomib (BTZ) and the immune modulator resiquimod (R848) were encapsulated individually and co-administered to investigate the synergistic chemo-immunotherapeutic efficacy in TNBC treatment. The biomimetic nanomicelles exhibited excellent biocompatibility and homologous targeting capacity, significantly enhancing drug delivery efficiency at the tumor site. studies demonstrated that biomimetic nanomicelles effectively induced tumor cell apoptosis, repolarized tumor-associated macrophages toward the M1 phenotype and promoted dendritic cell maturation. experiments further confirmed that the biomimetic nanomicelles markedly inhibited tumor growth and metastasis, enhanced antitumor immune responses, and exhibited strong synergy with BTZ to improve overall therapeutic outcomes in TNBC. This dual-action biomimetic nanomicelles delivery platform achieved efficient chemo-immunotherapeutic synergy and represents a promising strategy for targeted treatment of TNBC, with strong potential for clinical translation.
三阴性乳腺癌(TNBC)因其侵袭性本质仍然是一项临床挑战。传统的化学免疫疗法存在肿瘤靶向性差和全身毒性的问题,因此需要先进的递送系统来实现协同药物组合。本研究通过用4T1肿瘤细胞膜包覆纳米胶束构建了一种仿生纳米药物递送系统。该策略利用肿瘤细胞膜的同源靶向能力来提高纳米胶束在TNBC组织内的蓄积。将细胞毒性药物硼替佐米(BTZ)和免疫调节剂瑞喹莫德(R848)分别包封并共同给药,以研究其在TNBC治疗中的协同化学免疫治疗效果。仿生纳米胶束表现出优异的生物相容性和同源靶向能力,显著提高了肿瘤部位的药物递送效率。研究表明,仿生纳米胶束有效诱导肿瘤细胞凋亡,使肿瘤相关巨噬细胞重新极化至M1表型并促进树突状细胞成熟。实验进一步证实,仿生纳米胶束显著抑制肿瘤生长和转移,增强抗肿瘤免疫反应,并与BTZ表现出强大的协同作用,以改善TNBC的整体治疗效果。这种双作用仿生纳米胶束递送平台实现了高效的化学免疫治疗协同作用,代表了一种有前景的TNBC靶向治疗策略,具有很强的临床转化潜力。