Department of Animal Science, ARO, The Volcani Center, Rishon LeZion, Israel.
Koret School of Veterinary Medicine, Hebrew University of Jerusalem, Rehovot, Israel.
Gene Ther. 2024 Nov;31(11-12):580-586. doi: 10.1038/s41434-024-00495-5. Epub 2024 Oct 29.
Gene augmentation therapy is a promising treatment for incurable, blinding inherited retinal diseases, and intravitreal delivery is being studied as a safe alternative to subretinal injections. Adeno-Associated Viruses (AAV) are commonly-used vectors for ocular gene augmentation therapy. Naturally occurring pre-operative exposure and infection with AAV could result in presence of neutralizing antibodies (NAB's) in patients' serum, and may affect the safety and efficacy of treatment. Our aim was to characterize the humoral response against AAV pre- and post-intravitreal delivery of AAV2.7m8 vectors in a naturally-occurring sheep model of CNGA3 achromatopsia. Serial serum neutralization assays were performed to screen sheep for pre-exiting anti-AAV2 NAB's, and to assess the effect of intravitreal AAV2.7m8 injection on post-operative NAB titers and intraocular inflammation in sheep. The effect of viral dose and transgene type were also assessed. Serological screening revealed pre-operative seropositivity in 21.4% of animals, with age being a risk factor for the presence of anti-AAV2 NAB's. NAB titers increased following intravitreal AAV administration in the majority of sheep. There was no significant difference in the degree of post-operative serum neutralization between pre-operatively seronegative sheep and those with pre-existing antibodies. However, only sheep with pre-existing antibodies presented with signs of post-operative inflammation. We conclude that pre-existing anti-AAV2 NAB's do not affect the level of post-operative NAB titers; however, they increase the risk of post-operative ocular inflammation. Our results could have implications for the management of AAV-mediated ocular gene therapies, a technology being increasingly studied and used in patients.
基因增强疗法是治疗无法治愈的致盲遗传性视网膜疾病的一种有前途的方法,玻璃体内给药作为视网膜下注射的安全替代方法正在研究中。腺相关病毒 (AAV) 是眼科基因增强疗法中常用的载体。在手术前,AAV 的自然暴露和感染可能导致患者血清中存在中和抗体 (NAB),并可能影响治疗的安全性和疗效。我们的目的是在先天性 CNGA3 色盲羊模型中,描述 AAV2.7m8 载体玻璃体内给药前后针对 AAV 的体液反应。进行了一系列血清中和测定,以筛选预先存在抗 AAV2 NAB 的绵羊,并评估玻璃体内 AAV2.7m8 注射对术后 NAB 滴度和绵羊眼内炎症的影响。还评估了病毒剂量和转基因类型的影响。血清学筛查显示,21.4%的动物在手术前呈血清阳性,年龄是存在抗 AAV2 NAB 的危险因素。在大多数绵羊中,玻璃体内给予 AAV 后 NAB 滴度增加。在术前血清阴性的绵羊和预先存在抗体的绵羊之间,术后血清中和的程度没有显著差异。然而,只有预先存在抗体的绵羊出现术后炎症迹象。我们得出结论,预先存在的抗 AAV2 NAB 不会影响术后 NAB 滴度水平;但是,它们会增加术后眼部炎症的风险。我们的研究结果可能对 AAV 介导的眼部基因治疗的管理产生影响,该技术在患者中越来越受到研究和应用。