在etranacogene dezaparvovec 3期研究开始期间,成人血友病B患者中预先存在的AAV5抗体的自然历史

IF 4.7 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Therapy-Methods & Clinical Development Pub Date : 2025-08-18 eCollection Date: 2025-09-11 DOI:10.1016/j.omtm.2025.101568
Robert Klamroth, Michael Recht, Nigel S Key, Wolfgang Miesbach, Steven W Pipe, Radoslaw Kaczmarek, Douglass Drelich, Blanca Salazar, Sandra Le Quellec, Paul E Monahan, Nicholas Galante, Paul van der Valk, Jacqueline Tarrant
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引用次数: 0

摘要

检测腺相关病毒(AAV)的结合抗体或中和抗体(nab)是考虑AAV基因治疗的血友病患者实验室评估的一部分。在输注地扎帕洛韦前的3期临床试验中,我们评估了年龄≥18岁的B型血友病成年男性(因子IX≤2%)抗AAV血清型5 (AAV5)的NAb滴度的自然历史,以表征NAb以及免疫球蛋白G (IgG)和免疫球蛋白M (IgM)抗AAV5结合抗体随时间的变化。筛查时,48%(32/67)的参与者可检测到NAb (NAb+),中位滴度为58(范围:9-3,440)。参与者特定的引入期不同,包括停药(中位持续时间:240天;范围:1-360)。NAb滴度随时间变化的参与者内变异系数中位数为25%(范围:2%-154%)。NAb血清阳性与年龄相关(p = 0.0065)。对于检测到抗aav5抗体和IgG的参与者,每次就诊时滴度有很高的相关性(中位数r = 0.96;范围:0.92-0.99)。IgM抗aav5抗体仅在9%的参与者中检测到,且血清转化不常见。总之,AAV5 NAb检测结果在6个月内是一致的,这为考虑对B型血友病进行基因治疗提供了NAb筛查的时机。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Natural history of preexisting AAV5 antibodies in adults with hemophilia B during the lead-in of the etranacogene dezaparvovec phase 3 study.

Natural history of preexisting AAV5 antibodies in adults with hemophilia B during the lead-in of the etranacogene dezaparvovec phase 3 study.

Natural history of preexisting AAV5 antibodies in adults with hemophilia B during the lead-in of the etranacogene dezaparvovec phase 3 study.

Natural history of preexisting AAV5 antibodies in adults with hemophilia B during the lead-in of the etranacogene dezaparvovec phase 3 study.

Testing for binding or neutralizing antibodies (NAbs) to adeno-associated virus (AAV) is part of the laboratory assessment of people with hemophilia considering AAV-based gene therapy. We evaluated the natural history of NAb titers to AAV serotype 5 (AAV5) in adult males ≥18 years old with hemophilia B (factor IX ≤ 2%) during the lead-in period of a phase 3 trial prior to the infusion of etranacogene dezaparvovec to characterize NAb in addition to immunoglobulin G (IgG) and immunoglobulin M (IgM) anti-AAV5 binding antibody changes over time. At screening, 48% (32/67) of enrolled participants had detectable NAbs (NAb+) with a median titer of 58 (range: 9-3,440). Participant-specific lead-in periods differed and included discontinuers (median duration: 240 days; range: 1-360). The median intra-participant coefficient of variation of NAb titer over time was 25% (range: 2%-154%). NAb seropositivity was associated with older age (p = 0.0065). For participants with detectable anti-AAV5 NAbs and IgG, there was a high correlation of titers at each visit (median r = 0.96; range: 0.92-0.99). IgM anti-AAV5 antibodies were detectable in only 9% of participants, and seroconversion was infrequent. In conclusion, AAV5 NAb test results were consistent over 6 months, which informs the timing of NAb screening when considering gene therapy for hemophilia B.

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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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