Cationic Spherical Polypeptides with Immunogenic Cell Death Inducing Activity for Oncolytic Immunotherapy

IF 9.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Zhihui Guo, Tianze Huang, Renyong Yin, Yongchang Tian, Pengqi Wan, Xuan Yi, Gao Li, Peng Zhang, Chunsheng Xiao, Xuesi Chen
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引用次数: 0

Abstract

Immunogenic cell death (ICD) has gained increasing attention due to its capacity to trigger anticancer immunity. Herein, we report a series of fabricated cationic spherical polypeptides (CSPs) designated CSP-0 to CSP-57, with oncolytic activity and ICD-inducing ability. CSP-57 exerted the optimal broad-spectrum and tumor-cell-selective cytotoxicity by disrupting cell membranes and inducing cell necrosis. Moreover, CSP-57 damaged mitochondrial membranes, thereby elevating intracellular levels of reactive oxygen species, leading to robust ICD of tumor cells featured by multiple damage-associated molecular patterns, including calreticulin, high-mobility group box 1, and adenosine triphosphate. In vivo anticancer activity determination results suggested that CSP-57 significantly delayed B16F10 tumor growth in mice by direct oncolysis and subsequent induction of ICD. The immunotherapeutic efficacy of CSP-57 was characterized by elevated ratios of cytotoxic T cells in tumors and spleens. Briefly, this work indicates that CSPs represent a promising strategy for oncolytic immunotherapy.

用于肿瘤溶解免疫疗法的具有免疫原性细胞死亡诱导活性的阳离子球形多肽
免疫性细胞死亡(ICD)因其触发抗癌免疫的能力而日益受到关注。在此,我们报告了一系列具有溶瘤活性和ICD诱导能力的阳离子球形多肽(CSP),命名为CSP-0至CSP-57。CSP-57 通过破坏细胞膜和诱导细胞坏死,具有最佳的广谱性和肿瘤细胞选择性细胞毒性。此外,CSP-57还能破坏线粒体膜,从而提高细胞内活性氧的水平,导致肿瘤细胞的强ICD,其特征是多种损伤相关分子模式,包括钙网蛋白、高迁移率基团框1和三磷酸腺苷。体内抗癌活性测定结果表明,CSP-57通过直接溶瘤和随后的诱导ICD,显著延缓了小鼠体内B16F10肿瘤的生长。CSP-57的免疫治疗效果表现为肿瘤和脾脏中细胞毒性T细胞比例的升高。简而言之,这项研究表明,CSP 是一种很有前景的溶瘤免疫疗法策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CCS Chemistry
CCS Chemistry Chemistry-General Chemistry
CiteScore
13.60
自引率
13.40%
发文量
475
审稿时长
10 weeks
期刊介绍: CCS Chemistry, the flagship publication of the Chinese Chemical Society, stands as a leading international chemistry journal based in China. With a commitment to global outreach in both contributions and readership, the journal operates on a fully Open Access model, eliminating subscription fees for contributing authors. Issued monthly, all articles are published online promptly upon reaching final publishable form. Additionally, authors have the option to expedite the posting process through Immediate Online Accepted Article posting, making a PDF of their accepted article available online upon journal acceptance.
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