Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Department of Biomedical Engineering, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina 27599, United States.
ACS Nano. 2024 Mar 26;18(12):8733-8744. doi: 10.1021/acsnano.3c11165. Epub 2024 Mar 12.
Covalent conjugation of poly(ethylene glycol) (PEG) is frequently employed to enhance the pharmacokinetics and biodistribution of various protein and nanoparticle therapeutics. Unfortunately, some PEGylated drugs can induce elevated levels of antibodies that can bind PEG, i.e., anti-PEG antibodies (APA), in some patients. APA in turn can reduce the efficacy and increase the risks of allergic reactions, including anaphylaxis. There is currently no intervention available in the clinic that specifically mitigates allergic reactions to PEGylated drugs without the use of broad immunosuppression. We previously showed that infusion of high molecular weight free PEG could safely and effectively suppress the induction of APA in mice and restore prolonged circulation of various PEGylated therapeutics. Here, we explored the effectiveness of free PEG as a prophylaxis against anaphylaxis induced by PEG-specific allergic reactions in swine. Injection of PEG-liposomes (PL) resulted in anaphylactoid shock (pseudoanaphylaxis) within 1-3 min in both naïve and PL-sensitized swine. In contrast, repeated injection of free PEG alone did not result in allergic reactions, and injection of free PEG effectively suppressed allergic reactions to PL, including in previously PL-sensitized swine. These results strongly support the further investigation of free PEG for reducing APA and allergic responses to PEGylated therapeutics.
聚乙二醇(PEG)的共价结合常用于增强各种蛋白质和纳米颗粒治疗药物的药代动力学和生物分布。不幸的是,一些 PEG 化药物会在一些患者中诱导产生能结合 PEG 的抗体,即抗-PEG 抗体(APA)。APA 反过来又会降低疗效,并增加过敏反应的风险,包括过敏反应。目前临床上尚无专门用于减轻对 PEG 化药物过敏反应的干预措施,而无需广泛使用免疫抑制药物。我们之前的研究表明,输注高分子量游离 PEG 可安全有效地抑制小鼠中 APA 的诱导,并恢复各种 PEG 化治疗药物的延长循环。在这里,我们探索了游离 PEG 作为预防猪对 PEG 特异性过敏反应引起的过敏反应的有效性。PEG 脂质体(PL)的注射在 1-3 分钟内在未致敏和 PL 致敏的猪中导致过敏样休克(假性过敏反应)。相比之下,单独重复注射游离 PEG 不会引起过敏反应,并且游离 PEG 有效抑制了对 PL 的过敏反应,包括在先前 PL 致敏的猪中。这些结果强烈支持进一步研究游离 PEG 以减少 APA 和对 PEG 化治疗药物的过敏反应。