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可注射的活性氧响应型 SN38 前药支架与检查点抑制剂联合用于化学免疫治疗。

Injectable Reactive Oxygen Species-Responsive SN38 Prodrug Scaffold with Checkpoint Inhibitors for Combined Chemoimmunotherapy.

机构信息

Natural Products Research Center, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, Sichuan, P. R. China.

University of Chinese Academy of Sciences, Beijing 100049, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2020 Nov 11;12(45):50248-50259. doi: 10.1021/acsami.0c13943. Epub 2020 Nov 2.

Abstract

Chemotherapeutic agents have been widely used for cancer treatment in clinics. Aside from their direct cytotoxicity to cancer cells, some of them could activate the immune system of the host, contributing to the enhanced antitumor activity. Here, the reactive oxygen species (ROS)-responsive hydrogel, covalently cross-linked by phenylboronic acid-modified 7-ethyl-10-hydroxycamptothecin (SN38-SA-BA) with poly(vinyl alcohol) (PVA), is fabricated for topical delivery of anti-programmed cell death protein ligand 1 antibodies (aPDL1). In the presence of endogenous ROS, SN38-SA-BA will be oxidized and hydrolyzed, leading to the degradation of hydrogel and the release of initial free SN38 and encapsulated aPDL1. It is demonstrated that SN38 could elicit specific immune responses by triggering immunogenic cell death (ICD) of cancer cells, a distinct cell death pathway featured with the release of immunostimulatory damage-associated molecular patterns (DAMPs). Meanwhile, the released aPDL1 could bind to programmed cell death protein ligand 1 (PDL1) expressed on cancer cells to augment antitumor T cell responses. Thus, the ROS-responsive prodrug hydrogel loaded with aPDL1 could induce effective innate and adaptive antitumor immune responses after local injection, significantly inhibiting or even eliminating those tumors.

摘要

化疗药物在临床上被广泛用于癌症治疗。除了直接杀伤癌细胞外,其中一些还可以激活宿主的免疫系统,增强抗肿瘤活性。在这里,通过苯硼酸修饰的 7-乙基-10-羟基喜树碱(SN38-SA-BA)与聚乙烯醇(PVA)共价交联制备了用于局部递送抗程序性死亡配体 1 抗体(aPDL1)的活性氧(ROS)响应水凝胶。在内源性 ROS 的存在下,SN38-SA-BA 将被氧化和水解,导致水凝胶的降解和初始游离 SN38 和包封的 aPDL1 的释放。结果表明,SN38 可以通过触发癌细胞的免疫原性细胞死亡(ICD)引发特异性免疫反应,这是一种具有释放免疫刺激损伤相关分子模式(DAMPs)特征的独特细胞死亡途径。同时,释放的 aPDL1 可以与癌细胞表面表达的程序性死亡配体 1(PDL1)结合,增强抗肿瘤 T 细胞反应。因此,局部注射负载 aPDL1 的 ROS 响应前药水凝胶后,可诱导有效的先天和适应性抗肿瘤免疫反应,显著抑制甚至消除这些肿瘤。

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