Adeno-associated virus serotype 9 antibodies in neonates and young children: Seroprevalence and kinetics.

IF 4.6 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Therapy-Methods & Clinical Development Pub Date : 2024-09-21 eCollection Date: 2024-12-12 DOI:10.1016/j.omtm.2024.101344
Rudolf W van Olden, Christophe Lo Bianco, Keith W Dilly, Marina Savelieva, Siyan Xu, Aloys Tijsma, Carel van Baalen, Harsh Sharma, Nayla Mumneh
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引用次数: 0

Abstract

Gene therapies such as onasemnogene abeparvovec for spinal muscular atrophy (SMA) utilize adeno-associated virus 9 (AAV9) for targeted gene delivery, which requires an AAV9 antibody (AAV9-Ab) immunoglobulin G (IgG) ≤1:50 titer threshold. This retrospective cohort study evaluated age-related AAV9-Ab IgG seroprevalence for patients with SMA (part 1) and AAV9-Ab IgG kinetics and time to 1:50 titer threshold in newborns with elevated AAV9-Ab IgG titers (≥1:100) (part 2). A semi-quantitative ELISA assay was used in part 1 (N = 1,323 patients). For patients aged <12 months, 3.9% (n/N = 31/795) had elevated AAV9-Ab IgG titers (≥1:100); prevalence declined with age. In part 2, a new quantitative ELISA (linear mixed effects model) described continuous AAV9-Ab IgG concentrations for patients with initial titers ≥1:100. AAV9-Ab IgG concentrations waned according to first-order kinetics (58 samples; N = 18 patients). The model-based estimation of the AAV9-Ab IgG average half-life was 41 (95% CI, 38-44) days. Based on visualization, 200 ELISA units/mL was a reasonable approximate for the 1:50 titer threshold. In conclusion, initially elevated titers ≥1:100 in newborn patients declined with age. The new quantitative ELISA may allow for quantification of time to threshold for AAV9-Ab IgG retesting for onasemnogene abeparvovec treatment, leading to treatment as early as possible for patients with SMA.

腺相关病毒血清型9抗体在新生儿和幼儿:血清阳性率和动力学。
脊髓性肌萎缩症(SMA)的onasemnogene abparvovec等基因疗法利用腺相关病毒9 (AAV9)进行靶向基因递送,这需要AAV9抗体(AAV9- ab)免疫球蛋白G (IgG)≤1:50滴度阈值。本回顾性队列研究评估了SMA患者与年龄相关的AAV9-Ab IgG血清阳性率(第一部分),以及AAV9-Ab IgG滴度升高的新生儿(≥1:100)的AAV9-Ab IgG动力学和达到1:50滴度阈值的时间(第二部分)。第一部分采用半定量ELISA法(N = 1,323例患者)。年龄(n/ n = 31/795)的患者AAV9-Ab IgG滴度升高(≥1:100);患病率随着年龄的增长而下降。在第2部分中,一种新的定量ELISA(线性混合效应模型)描述了初始滴度≥1:100的患者的连续AAV9-Ab IgG浓度。根据一级动力学,AAV9-Ab - IgG浓度下降(58个样本;N = 18例)。基于模型估计的AAV9-Ab - IgG平均半衰期为41天(95% CI, 38-44)。根据可视化结果,200个ELISA单位/mL是1:50滴度阈值的合理近似。总之,在新生儿患者中,初始升高的滴度≥1:100随着年龄的增长而下降。新的定量ELISA可以量化AAV9-Ab - IgG重新检测阿伯帕韦治疗的阈值时间,从而使SMA患者尽早治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Therapy-Methods & Clinical Development
Molecular Therapy-Methods & Clinical Development Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.90
自引率
4.30%
发文量
163
审稿时长
12 weeks
期刊介绍: The aim of Molecular Therapy—Methods & Clinical Development is to build upon the success of Molecular Therapy in publishing important peer-reviewed methods and procedures, as well as translational advances in the broad array of fields under the molecular therapy umbrella. Topics of particular interest within the journal''s scope include: Gene vector engineering and production, Methods for targeted genome editing and engineering, Methods and technology development for cell reprogramming and directed differentiation of pluripotent cells, Methods for gene and cell vector delivery, Development of biomaterials and nanoparticles for applications in gene and cell therapy and regenerative medicine, Analysis of gene and cell vector biodistribution and tracking, Pharmacology/toxicology studies of new and next-generation vectors, Methods for cell isolation, engineering, culture, expansion, and transplantation, Cell processing, storage, and banking for therapeutic application, Preclinical and QC/QA assay development, Translational and clinical scale-up and Good Manufacturing procedures and process development, Clinical protocol development, Computational and bioinformatic methods for analysis, modeling, or visualization of biological data, Negotiating the regulatory approval process and obtaining such approval for clinical trials.
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