Department of Pharmaceutical Engineering, School of Engineering, China Pharmaceutical University, Nanjing 210009, PR China.
Biomater Sci. 2019 Jun 25;7(7):2749-2758. doi: 10.1039/c9bm00324j.
Combining chemotherapy and immunotherapy has been considered as an attractive approach to improve cancer therapy. Here we prepared folated PVA-based nanogels for the simultaneous delivery of docetaxel (DTX) and the indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor NLG919 (N9) for enhancing cancer chemo-immunotherapy. FDA-approved poly(vinyl alcohol) (PVA) with good biocompatibility was modified with vinyl ether acrylate (VEA) groups for UV-crosslinking and acidic degradation. Carboxyl groups were introduced via modification with succinic anhydride for improved drug loading and folic acid (FA) ligands were incorporated for tumor targeting. UV-crosslinked folated PVA nanogels were efficiently taken up by tumor cells followed by endo/lysosomal pH-triggered intracellular drug release, which induced significant cytotoxicity towards 4T1 breast cancer cells in vitro. DTX and N9 co-loaded PVA nanogels exhibited a much higher antitumor efficiency in 4T1 mouse breast cancer models in vivo as compared to the free drug controls. The drug-laden nanogels not only directly killed the tumor cells by DTX, but also induced immunogenic cell death (ICD) promoting intratumoral accumulation of cytotoxic T lymphocytes, and further combining with N9 elevated the intratumoral infiltration of CD8+ T cells and NK cells and inhibited the infiltration of MDSCs, downregulating IDO1-mediated immunosuppression.
联合化疗和免疫疗法被认为是提高癌症治疗效果的一种有吸引力的方法。在这里,我们制备了叶酸化聚乙烯醇(PVA)纳米凝胶,用于同时递送多西紫杉醇(DTX)和吲哚胺 2,3-双加氧酶 1(IDO1)抑制剂 NLG919(N9),以增强癌症化疗免疫治疗。经过改良的聚(乙烯醇)(PVA)具有良好的生物相容性,用乙烯醚丙烯酸酯(VEA)基团进行 UV 交联和酸性降解。通过与琥珀酸酐反应引入羧基基团以提高药物载量,并掺入叶酸(FA)配体以实现肿瘤靶向。经 UV 交联的叶酸化 PVA 纳米凝胶被肿瘤细胞有效摄取,随后在内涵体/溶酶体 pH 触发下发生细胞内药物释放,这导致体外 4T1 乳腺癌细胞产生显著的细胞毒性。与游离药物对照相比,载有 DTX 和 N9 的 PVA 纳米凝胶在 4T1 小鼠乳腺癌模型中的体内抗肿瘤效率要高得多。载药纳米凝胶不仅通过 DTX 直接杀死肿瘤细胞,还诱导免疫原性细胞死亡(ICD),促进细胞毒性 T 淋巴细胞在肿瘤内积聚,进一步与 N9 结合可提高肿瘤内 CD8+T 细胞和 NK 细胞的浸润,并抑制 MDSC 的浸润,下调 IDO1 介导的免疫抑制。