乙二醇
补体系统
脂质体
PEG比率
体内
药品
药理学
免疫系统
材料科学
化学
纳米技术
医学
免疫学
生物
有机化学
生物技术
经济
财务
作者
Alberto Gabizón,János Szebeni
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-07-09
卷期号:14 (7): 7682-7688
被引量:72
标识
DOI:10.1021/acsnano.0c03648
摘要
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.
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