Prevalence of adeno-associated virus type 3B neutralizing antibodies in cohorts of healthy donors and Wilson's disease adults.

IF 5.9 3区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Céline Bouquet, Blanche Tamarit, Gloria Gonzalez Aseguinolaza, Veronica Ferrer, Sonia Valero, Anne Douar, Annelise Brossel, Rainard Fuhr, Jean-Philippe Combal
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Abstract

Adeno-associated virus (AAV) is widely used for liver-directed gene therapy, with AAV serotype 3B (AAV3B) showing particularly high tropism for human hepatocytes. However, pre-existing neutralizing antibodies (NAbs) against AAV represent a major barrier to efficient gene transfer and patient eligibility. We have recently demonstrated that subjects with intermediate NAb levels (1:5-1:45), that would be excluded from clinical trials, can be converted in eligible patients by the administration of IgG-cleaving enzymes. It is thus crucial to assess not only the seroprevalence but also titer distribution. Here, we analyzed anti-AAV3B NAb titers, using a validated cell-based transduction inhibition assay, in healthy adults and patients with Wilson's disease, a hepatic metabolic disorder amenable to AAV3B-mediated gene therapy. Two independent cohorts of healthy adults (n = 200 and n = 580) were analyzed; 33-36% of individuals were NAb positive, and prevalence increased with age. Differences were observed across ethnicities. Importantly, a substantial proportion of seropositive individuals (19%) exhibited intermediate NAb titers. In contrast, only 17.4% of Wilson's disease patients (n = 23) were positive, all with high NAb titers. These findings provide insights into target population eligibility, and titer distribution data support the potential of NAb-reduction approaches to expand access to systemic AAV3B-based gene therapies.

腺相关病毒3B型中和抗体在健康供体和成年威尔逊氏病人群中的流行
腺相关病毒(AAV)广泛用于肝脏定向基因治疗,AAV血清型3B (AAV3B)对人肝细胞表现出特别高的嗜性。然而,针对AAV的预先存在的中和抗体(nab)是有效基因转移和患者资格的主要障碍。我们最近证明,被排除在临床试验之外的中等NAb水平(1:5-1:45)的受试者可以通过给药igg切割酶在符合条件的患者中转化。因此,不仅要评估血清阳性率,还要评估滴度分布,这一点至关重要。在这里,我们分析了抗aav3b NAb滴度,使用了一种有效的基于细胞的转导抑制试验,在健康成人和威尔森病(一种肝脏代谢紊乱,适合aav3b介导的基因治疗)患者中。对两个独立的健康成人队列(n = 200和n = 580)进行分析;33-36%的人NAb阳性,患病率随年龄增长而增加。不同种族之间存在差异。重要的是,相当大比例的血清阳性个体(19%)表现出中等NAb滴度。相比之下,只有17.4%的威尔逊氏病患者(n = 23)呈阳性,均为高NAb滴度。这些发现为目标人群的适格性提供了见解,滴度分布数据支持了nab减少方法扩大基于aav3b的系统性基因治疗的潜力。
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来源期刊
Gene Therapy
Gene Therapy 医学-生化与分子生物学
CiteScore
9.70
自引率
2.00%
发文量
67
审稿时长
4-8 weeks
期刊介绍: Gene Therapy covers both the research and clinical applications of novel therapeutic techniques based on a genetic component. Over the last few decades, significant advances in technologies ranging from identifying novel genetic targets that cause disease through to clinical studies, which show therapeutic benefit, have elevated this multidisciplinary field to the forefront of modern medicine.
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