Institute for Bioprocessing and Analytical Measurement Techniques, 37308 Heiligenstadt, Germany.
Department of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745 Jena, Germany.
Bioconjug Chem. 2022 Aug 17;33(8):1574-1583. doi: 10.1021/acs.bioconjchem.2c00316. Epub 2022 Jul 25.
The pentasaccharide Fondaparinux, a synthetic selective factor Xa inhibitor, is one of the safest anticoagulants in the heparin family that is recommended as an alternative drug for patients with hypersensitivity to other drugs such as heparin-induced thrombocytopenia (HIT). However, some observations of Fondaparinux-induced thrombocytopenia (FIT) have been reported while others claimed that FIT does not occur in patients with fondaparinux therapy, indicating that the mechanism of FIT remains controversial. Here, we utilized different methodologies including dynamic light scattering, immunosorbent and platelet aggregation assays, confocal laser scanning microscopy, and flow cytometry to gain insights into FIT. We found that at a certain concentration, Fondaparinux formed sufficient large and stable complexes with PF4 that facilitated binding of the HIT-like monoclonal KKO antibody and enhanced platelet aggregation and activation. We proposed a model to describe the role of Fondaparinux concentration in the formation of complexes with platelet factor 4 and how it promotes the binding of KKO. Our results clarify controversial observations of FIT in patients as each contains a dissimilar PF4:Fondaparinux concentration ratio.
戊聚糖磺达肝素钠是一种合成的、选择性的 Xa 因子抑制剂,是肝素类药物中最安全的抗凝剂之一,被推荐作为对其他药物(如肝素诱导的血小板减少症 [HIT])过敏的患者的替代药物。然而,一些观察结果表明存在磺达肝素钠诱导的血小板减少症(FIT),而另一些则声称在接受磺达肝素钠治疗的患者中不会发生 FIT,表明 FIT 的机制仍存在争议。在这里,我们使用了包括动态光散射、免疫吸附和血小板聚集测定、共聚焦激光扫描显微镜和流式细胞术在内的不同方法学来深入了解 FIT。我们发现,在一定浓度下,磺达肝素钠与 PF4 形成了足够大且稳定的复合物,促进了 HIT 样单克隆抗体 KKO 的结合,并增强了血小板聚集和激活。我们提出了一个模型来描述磺达肝素钠浓度在与血小板因子 4 形成复合物中的作用,以及它如何促进 KKO 的结合。我们的结果澄清了 FIT 在患者中的有争议的观察结果,因为每个结果都包含不同的 PF4:磺达肝素钠浓度比。