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Anti-PEG IgM production and accelerated blood clearance phenomenon after the administration of PEGylated exosomes in mice

微泡 聚乙二醇化 外体 PEG比率 化学 体内 药理学 胞外囊泡 聚乙二醇 脂质体 药代动力学 医学 药物输送 生物 生物化学 小RNA 生物技术 经济 基因 财务
作者
Sherif E. Emam,Nehal E. Elsadek,Amr S. Abu Lila,Haruka Takata,Yoshino Kawaguchi,Toshifumi Shimizu,Hidenori Ando,Yu Ishima,Tatsuhiro Ishida
出处
期刊:Journal of Controlled Release [Elsevier]
卷期号:334: 327-334 被引量:16
标识
DOI:10.1016/j.jconrel.2021.05.001
摘要

Recently, there is an increasing interest in exosomes or extracellular vesicles as potential candidates for delivering RNAs, proteins, genes, and anticancer agents. Engineering of exosome properties is rapidly evolving as a means of expanding exosome applications. PEGylation of exosomes is a technique used to improve their in vivo stability, circulation half-lives, and sometimes to allow the binding targeting ligands to the exosome exterior. According to FDA guidelines for the development of PEGylated proteins, immunological responses to PEGylated molecules and particles should be examined. In this study, we prepared PEGylated exosomes and investigated the production of anti-PEG IgM antibodies after single i.v. injections in mice. In addition, we monitored blood concentrations and tumor accumulation of a second dose of PEGylated exosomes administered after the initial dose. Single injections of PEGylated exosomes in mice induced anti-PEG IgM production in a T cell-dependent manner. The anti-PEG IgM production decreased when the injection dose of PEGylated exosomes was further increased. Anti-PEG IgM induced by injection of PEGylated exosomes decreased blood concentrations of a second dose of PEGylated exosomes and suppressed their tumor accumulation in a C26 murine colorectal cancer model. Initial injection doses of either PEGylated liposomes or PEGylated ovalbumin (PEG-OVA), both of them induced anti-PEG IgM production, also decreased the blood concentration of PEGylated exosomes. Interestingly, anti-PEG IgM induced by injection of PEGylated exosomes did not affect the blood concentration of PEG-OVA. These results imply the importance of monitoring anti-PEG IgM when repeat PEGylated exosome doses are required and/or when PEGylated exosomes are used together with other PEGylated therapeutics. • PEGylated exosomes induce anti-PEG IgM in a T-cell dependent manner. • Accelerated blood clearance (ABC) phenomenon is observed in PEGylated exosomes. • The ABC phenomenon reduces tumor accumulation of second dose of PEGylated exosomes.
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