Department of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Blood. 2010 Dec 23;116(26):5842-8. doi: 10.1182/blood-2010-06-288001. Epub 2010 Sep 28.
Inhibitory antibodies to factor VIII (FVIII) are a major complication in the treatment of hemophilia A, affecting approximately 20% to 30% of patients. Current treatment for inhibitors is based on long-term, daily injections of large amounts of FVIII protein. Liver-directed gene therapy has been used to induce antigen-specific tolerance, but there are no data in hemophilic animals with pre-existing inhibitors. To determine whether sustained endogenous expression of FVIII could eradicate inhibitors, we injected adeno-associated viral vectors encoding canine FVIII (cFVIII) in 2 strains of inhibitor hemophilia A dogs. In 3 dogs, a transient increase in inhibitor titers (up to 7 Bethesda Units [BU]) at 2 weeks was followed by continuous decline to complete disappearance within 4-5 weeks. Subsequently, an increase in cFVIII levels (1.5%-8%), a shortening of clotting times, and a reduction (> 90%) of bleeding episodes were observed. Immune tolerance was confirmed by lack of antibody formation after repeated challenges with cFVIII protein and normal protein half-life. A fourth dog exhibited a strong early anamnestic response (216 BU), with slow decline to 0.8 BU and cFVIII antigen detection by 18 months after vector delivery. These data suggest that liver gene therapy has the potential to eradicate inhibitors and could improve the outcomes of hemophilia A patients.
抑制性抗体针对因子 VIII(FVIII)是治疗甲型血友病的主要并发症,约影响 20%至 30%的患者。目前针对抑制剂的治疗基于长期、每日大剂量 FVIII 蛋白注射。肝靶向基因治疗已被用于诱导抗原特异性耐受,但在有预先存在抑制剂的血友病动物中尚无数据。为了确定持续内源性表达 FVIII 是否可以消除抑制剂,我们在 2 种抑制剂甲型血友病犬中注射了编码犬 FVIII(cFVIII)的腺相关病毒载体。在 3 只狗中,在 2 周时抑制剂滴度(高达 7 个 Bethesda 单位[BU])短暂增加,随后持续下降,4-5 周内完全消失。随后,cFVIII 水平增加(1.5%-8%),凝血时间缩短,出血事件减少(>90%)。通过反复接受 cFVIII 蛋白和正常蛋白半衰期的挑战,确认免疫耐受,无抗体形成。第四只狗表现出强烈的早期回忆反应(216 BU),在载体输送后 18 个月下降至 0.8 BU 和 cFVIII 抗原检测。这些数据表明,肝基因治疗有可能消除抑制剂,并可能改善甲型血友病患者的结局。