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补体激活:聚乙二醇包被纳米药物安全性的潜在威胁

Complement Activation: A Potential Threat on the Safety of Poly(ethylene glycol)-Coated Nanomedicines.

作者信息

Gabizon Alberto, Szebeni Janos

机构信息

Nano-oncology Research Center, Shaare Zedek Medical Center and The Hebrew University-Faculty of Medicine, Jerusalem 9103102, Israel.

Lipomedix Pharmaceuticals Ltd., Jerusalem 9139102, Israel.

出版信息

ACS Nano. 2020 Jul 28;14(7):7682-7688. doi: 10.1021/acsnano.0c03648. Epub 2020 Jul 9.

Abstract

In this issue of , Chen provide and evidence for monoclonal anti-poly(ethylene glycol) (anti-PEG) antibody-triggered, complement terminal complex-mediated damage to PEGylated liposomal doxorubicin, entailing the release of the encapsulated drug from the vesicles. These results reveal a new dimension of the potential damage of anti-PEG antibody-mediated complement activation on PEGylated nanomedicines in addition to previous observations on infusion hypersensitivity reactions and the accelerated blood clearance effect. The possibility of a destructive attack of the complement system on the liposome drug carrier may have safety implications in patients displaying high levels of preformed anti-PEG antibodies. In this Perspective, we summarize the experimental and clinical data highlighting the relationships among the above adverse immune phenomena and the options available for reducing the risk of immune damage caused by PEGylated nanomedicines.

摘要

在本期杂志中,陈等人提供了单克隆抗聚乙二醇(抗PEG)抗体引发、补体末端复合物介导的对聚乙二醇化脂质体阿霉素损伤的证据,这会导致包封药物从囊泡中释放。这些结果揭示了抗PEG抗体介导的补体激活对聚乙二醇化纳米药物潜在损伤的一个新层面,这是除了之前关于输注超敏反应和加速血液清除效应的观察之外的。补体系统对脂质体药物载体进行破坏性攻击的可能性,对于显示高水平预先形成的抗PEG抗体的患者可能具有安全意义。在这篇观点文章中,我们总结了突出上述不良免疫现象之间关系的实验和临床数据,以及降低聚乙二醇化纳米药物引起免疫损伤风险的可用选项。

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