Nanomedicine Research and Education Center, Institute of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.
SeroScience LCC., Cambridge, MA 02138, USA and 1089 Budapest, Hungary.
Molecules. 2019 Sep 9;24(18):3283. doi: 10.3390/molecules24183283.
Complement (C) activation can underlie the infusion reactions to liposomes and other nanoparticle-based medicines, a hypersensitivity syndrome that can be partially reproduced in animal models. However, the sensitivities and manifestations substantially differ in different species, and C activation may not be the only cause of pathophysiological changes. In order to map the species variation of C-dependent and -independent pseudoallergy (CARPA/CIPA), here we used known C activators and C activator liposomes to compare their acute hemodynamic, hematological, and biochemical effects in rats. These C activators were cobra venom factor (CVF), zymosan, AmBisome (at 2 doses), its amphotericin B-free vehicle (AmBisombo), and a PEGylated cholesterol-containing liposome (PEG-2000-chol), all having different powers to activate C in rat blood. The pathophysiological endpoints measured were blood pressure, leukocyte and platelet counts, and plasma thromboxane B2, while C activation was assessed by C3 consumption using the Pan-Specific C3 assay. The results showed strong linear correlation between C activation and systemic hypotension, pointing to a causal role of C activation in the hemodynamic changes. The observed thrombocytopenia and leukopenia followed by leukocytosis also correlated with C3 conversion in case of C activators, but not necessarily with C activation by liposomes. These findings are consistent with the double hit hypothesis of hypersensitivity reactions (HSRs), inasmuch as strong C activation can fully account for all symptoms of HSRs, but in case of no-, or weak C activators, the pathophysiological response, if any, is likely to involve other activation pathways.
补体 (C) 激活可能是脂质体和其他基于纳米颗粒的药物输注反应的基础,这是一种超敏反应综合征,在动物模型中可以部分重现。然而,不同物种的敏感性和表现有很大差异,C 激活可能不是病理生理变化的唯一原因。为了绘制 C 依赖性和非依赖性假性过敏(CARPA/CIPA)的物种变异图谱,我们在这里使用已知的 C 激活剂和 C 激活脂质体来比较它们在大鼠中的急性血液动力学、血液学和生化效应。这些 C 激活剂是眼镜蛇毒液因子 (CVF)、酵母聚糖、AmBisome(两种剂量)、其不含两性霉素 B 的载体 (AmBisombo) 和含有聚乙二醇化胆固醇的脂质体 (PEG-2000-chol),它们在大鼠血液中激活 C 的能力不同。测量的病理生理终点是血压、白细胞和血小板计数以及血浆血栓素 B2,而 C 激活则使用 Pan-Specific C3 测定通过 C3 消耗来评估。结果表明,C 激活与全身低血压之间存在强烈的线性相关性,这表明 C 激活在血液动力学变化中起因果作用。观察到的血小板减少症和白细胞减少症随后出现白细胞增多症也与 C 激活剂的 C3 转化相关,但与脂质体的 C 激活不一定相关。这些发现与超敏反应 (HSR) 的双打击假说一致,因为强烈的 C 激活可以完全解释 HSR 的所有症状,但在没有或弱 C 激活剂的情况下,如果存在病理生理反应,则可能涉及其他激活途径。