Hsieh Ming-Shou, Liu Heng-Wei, Guo Fu-You, Song Deng-Pan, Li Meng-Yuan, Chao Tsu-Yi, Fong Iat-Hang, Chang Yu-Sheng, Yeh Chi-Tai
Department of Medical Research & Education, Taipei Medical University- Shuang Ho Hospital, New Taipei 23561, Taiwan.
Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan; Division of Neurosurgery, Department of Surgery, Taipei Medical University-Shuang Ho Hospital, New Taipei 23561, Taiwan; Taipei Neuroscience Institute, Taipei Medical University, Taipei 11031, Taiwan.
Biomed Pharmacother. 2025 May;186:117968. doi: 10.1016/j.biopha.2025.117968. Epub 2025 Mar 22.
Clinically used in systemic lupus erythematosus (SLE), Hydroxychloroquine (HCQ) exerts antithrombotic effects by inhibiting anti-β2-glycoprotein I (anti-β2GPI) antibody binding to phospholipid bilayers. However, HCQ is a racemic mixture, with only one enantiomer offering therapeutic benefits, while the other may contribute to toxicity. The current study evaluated the thromboprophylactic efficacy of R-enantiomer Hydroxychloroquine (R-HCQ), S-enantiomer Hydroxychloroquine (S-HCQ), and racemic HCQ (Rac-HCQ), with a focus on their impact on APS-associated markers. Both in vitro and in vivo models were employed, with human umbilical vein endothelial cells (HUVECs) and mice immunized with human β2-glycoprotein I antibodies used to evaluate the formation of antiphospholipid thrombotic complexes and their modulation by HCQ enantiomers. S-HCQ significantly reduced β2GPI complex binding and restored the AnxA5 anticoagulant shield in vitro, demonstrating superior efficacy over R-HCQ in disrupting β2GPI/anti-β2GPI interactions and preventing endothelial dysfunction in APS models. Pretreatment of HUVECs with S-HCQ significantly attenuated the expression of proinflammatory cytokines (tumor necrosis factor-alpha, interleukin-6, interleukin-1 beta, and C-C motif ligand 2) and endothelial activation markers (intercellular adhesion molecule 1, vascular cell adhesion molecule 1, and E-selectin). S-HCQ alleviates endothelial dysfunction by reducing proinflammatory cytokines, endothelial activation markers, and NO production while downregulating iNOS expression, highlighting its potential to mitigate oxidative stress and thrombogenic activity in APS-related endothelial damage. In vivo, S-HCQ effectively reduced clot formation in the femoral veins of APS mouse models. Among the HCQ enantiomers tested, S-HCQ demonstrated superior efficacy in modulating inflammatory and angiogenic pathways, influencing the formation of antiphospholipid thrombotic complexes and mitigating thrombosis. These findings underscore the potential of S-HCQ as a therapeutic alternative for APS management.
羟氯喹啉(HCQ)临床用于治疗系统性红斑狼疮(SLE),它通过抑制抗β2糖蛋白I(抗β2GPI)抗体与磷脂双层的结合发挥抗血栓作用。然而,HCQ是一种外消旋混合物,只有一种对映体具有治疗益处,而另一种可能会导致毒性。本研究评估了R-对映体羟氯喹啉(R-HCQ)、S-对映体羟氯喹啉(S-HCQ)和外消旋HCQ(Rac-HCQ)的血栓预防效果,重点关注它们对抗磷脂综合征(APS)相关标志物的影响。研究采用了体外和体内模型,用人脐静脉内皮细胞(HUVECs)和用人β2糖蛋白I抗体免疫的小鼠来评估抗磷脂血栓复合物的形成以及HCQ对映体对其的调节作用。S-HCQ在体外显著降低了β2GPI复合物的结合,并恢复了膜联蛋白A5抗凝屏障,在破坏β2GPI/抗β2GPI相互作用和预防APS模型中的内皮功能障碍方面显示出优于R-HCQ的疗效。用S-HCQ预处理HUVECs可显著减弱促炎细胞因子(肿瘤坏死因子-α、白细胞介素-6、白细胞介素-1β和C-C基序配体2)和内皮激活标志物(细胞间黏附分子1、血管细胞黏附分子1和E-选择素)的表达。S-HCQ通过减少促炎细胞因子、内皮激活标志物和一氧化氮的产生,同时下调诱导型一氧化氮合酶的表达来减轻内皮功能障碍,突出了其减轻APS相关内皮损伤中氧化应激和血栓形成活性的潜力。在体内,S-HCQ有效减少了APS小鼠模型股静脉中的血栓形成。在所测试的HCQ对映体中,S-HCQ在调节炎症和血管生成途径、影响抗磷脂血栓复合物的形成以及减轻血栓形成方面显示出卓越的疗效。这些发现强调了S-HCQ作为APS治疗替代方案的潜力。