Zhang Yuyang, Liu Tingting, Kou Haiming, Wang Huafang, Hu Yu, Tang Liang V
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Gene Ther. 2025 May 24. doi: 10.1038/s41434-025-00541-w.
Heparin cofactor II (HCII) is a critical anticoagulant protein that inactivates thrombin. In our previous mouse studies, we demonstrated that GalNAc-HCII, a small interfering RNA (siRNA) targeting HCII conjugated with N-acetylgalactosamine (GalNAc), exhibited promising therapeutic effects in hemophilia A mouse models. Further evaluation in large animal models, especially with FVIII inhibitors, is essential before GalNAc-HCII can proceed to clinical trials. In this study, we successfully established, for the first time, an acquired hemophilia A canine model by multiple intravenous injections of a rabbit-dog chimeric neutralizing anti-canine FVIII antibody. In the control group, the Beagle dogs exhibited spontaneous bleeding symptoms accompanied by prolonged activated partial thromboplastin time (APTT). After administration, GalNAc-HCII (0.8 and 1.6 mg/kg) demonstrated potent, dose-dependent, and durable HCII inhibitory effects. After 5 days, in normal dogs, GalNAc-HCII reduced HCII levels to 32.67% ± 3.07% and 10.62% ± 1.74% with 0.8 and 1.6 mg/kg GalNAc-HCII, respectively. In hemophilic dogs, GalNAc-HCII treatment significantly improved hemostatic function. Specifically, in the carotid artery thrombosis model, the thrombus formation time was shortened [29.7 ± 2.08 min (0.8 mg/kg) and 18.0 ± 1.0 min (1.6 mg/kg) vs. 40 min (control), P < 0.01]; in the knee joint puncture-induced bleeding model, joint bleeding and synovitis were alleviated; and in the saphenous vein bleeding model, the number of hemostatic events increased. Furthermore, repeated administration of GalNAc-HCII effectively reduced the prolonged APTT. This study demonstrates the efficacy of GalNAc-HCII in hemophilic dogs, suggesting it as a promising novel therapeutic option for patients with hemophilia, including those with FVIII inhibitors.
肝素辅因子II(HCII)是一种使凝血酶失活的关键抗凝蛋白。在我们之前的小鼠研究中,我们证明了GalNAc-HCII,一种与N-乙酰半乳糖胺(GalNAc)偶联的靶向HCII的小干扰RNA(siRNA),在A型血友病小鼠模型中显示出有前景的治疗效果。在GalNAc-HCII能够进入临床试验之前,在大型动物模型中进行进一步评估至关重要,尤其是对于存在FVIII抑制剂的情况。在本研究中,我们首次通过多次静脉注射兔-犬嵌合中和抗犬FVIII抗体成功建立了获得性A型血友病犬模型。在对照组中,比格犬表现出自发性出血症状,同时活化部分凝血活酶时间(APTT)延长。给药后,GalNAc-HCII(0.8和1.6mg/kg)表现出强效、剂量依赖性和持久的HCII抑制作用。5天后,在正常犬中,GalNAc-HCII分别以0.8和1.6mg/kg的剂量将HCII水平降低至32.67%±3.07%和10.62%±1.74%。在血友病犬中,GalNAc-HCII治疗显著改善了止血功能。具体而言,在颈动脉血栓形成模型中,血栓形成时间缩短[29.7±2.08分钟(0.8mg/kg)和18.0±1.0分钟(1.6mg/kg)对比40分钟(对照组),P<0.01];在膝关节穿刺诱导的出血模型中,关节出血和滑膜炎得到缓解;在大隐静脉出血模型中,止血事件数量增加。此外,重复给药GalNAc-HCII有效缩短了延长的APTT。本研究证明了GalNAc-HCII在血友病犬中的疗效,表明它是血友病患者(包括那些存在FVIII抑制剂的患者)一种有前景的新型治疗选择。