Department of Pharmaceutics, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, 44 Wenhua Xi Road, Jinan, Shandong 250012, China.
ACS Appl Mater Interfaces. 2021 May 19;13(19):22213-22224. doi: 10.1021/acsami.1c03709. Epub 2021 May 6.
Lymph nodes are the main sites for immune activation and surveillance. Effective delivery of immunomodulators into lymph nodes to trigger antitumor immunity is essential for cancer treatment. Here, we propose a lymph node delivery strategy to modulate the immune response by activating cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells simultaneously. Novel pH/redox dual-sensitive micelles were prepared using poly(l-histidine)-poly(ethylene glycol) (PLH-PEG) as a skeleton, which can effectively deliver immunomodulators to the lymph nodes due to their suitable particle size. At 48 h after subcutaneous injection, the accumulation efficiency in lymph nodes increased 8.12-fold compared with the control group. Subsequently, Trp2/CpG-coloaded pH/redox dual-sensitive micelles (Trp2/CpG-NPs) acted on antigen-presenting cells, fully promoting CTL activation through dendritic cell antigen cross-presentation and macrophage repolarization. IL-15-loaded pH/redox dual-sensitive micelles (IL-15-NPs) were developed to activate the killing effect of NK cells by interacting with IL-15 receptors. In the tumor-bearing mice model, this lymph node delivery strategy showed significant antitumor efficiency and the tumor inhibition rate reached 93.76%. Meanwhile, the infiltration of CTLs and NK cells in tumor tissues increased, and the immunosuppressive microenvironment was relieved by the repolarization of macrophages from M2-type to M1-type. Overall, this study highlighted the potential of the lymph node delivery strategy for cancer immunotherapy.
淋巴结是免疫激活和监测的主要部位。将免疫调节剂有效递送至淋巴结以触发抗肿瘤免疫对于癌症治疗至关重要。在这里,我们提出了一种淋巴结递药策略,通过同时激活细胞毒性 T 淋巴细胞(CTL)和自然杀伤(NK)细胞来调节免疫反应。使用聚(组氨酸)-聚乙二醇(PLH-PEG)作为骨架制备了新型的 pH/氧化还原双重敏感胶束,由于其合适的粒径,能够将免疫调节剂有效递送至淋巴结。在皮下注射后 48 小时,与对照组相比,淋巴结中的积累效率增加了 8.12 倍。随后,色氨酸/CpG 共载 pH/氧化还原双重敏感胶束(Trp2/CpG-NPs)作用于抗原呈递细胞,通过树突状细胞抗原交叉呈递和巨噬细胞重极化充分促进 CTL 的激活。开发了负载白细胞介素 15(IL-15)的 pH/氧化还原双重敏感胶束(IL-15-NPs),通过与白细胞介素 15 受体相互作用来激活 NK 细胞的杀伤效应。在荷瘤小鼠模型中,这种淋巴结递药策略表现出显著的抗肿瘤效率,肿瘤抑制率达到 93.76%。同时,CTL 和 NK 细胞在肿瘤组织中的浸润增加,并且巨噬细胞从 M2 型向 M1 型的重极化缓解了免疫抑制微环境。总的来说,这项研究强调了淋巴结递药策略在癌症免疫治疗中的潜力。