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
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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