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正常和肌营养不良犬对 AAV-6、8 和 9 的体液免疫。

Humoral immunity to AAV-6, 8, and 9 in normal and dystrophic dogs.

机构信息

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO 65212, USA.

出版信息

Hum Gene Ther. 2012 Mar;23(3):287-94. doi: 10.1089/hum.2011.125. Epub 2012 Jan 11.

Abstract

Adeno-associated virus (AAV)-6, 8, and 9 are promising gene-delivery vectors for testing novel Duchenne muscular dystrophy gene therapy in the canine model. Humoral immunity greatly influences in vivo AAV transduction. However, neutralizing antibodies to AAV-6, 8, and 9 have not been systemically examined in normal and dystrophic dogs. To gain information on the seroprevalence of antibodies to AAV-6, 8, and 9, we measured neutralizing antibody titers using an in vitro transduction inhibition assay. We examined 72 naive serum samples and 26 serum samples obtained from dogs that had received AAV gene transfer. Our data demonstrated that AAV-6 neutralizing antibody was the most prevalent antibody in dogs irrespective of age, gender, disease status (dystrophic or not), and prior parvovirus vaccination history. Surprisingly, high-level anti-AAV-6 antibody was detected at birth in newborn puppies. Further, a robust antibody response was induced in affected, but not normal newborn dogs following systemic AAV gene transfer. Taken together, our data have provided an important baseline on the seroprevalence of AAV-6, 8, and 9 neutralizing antibodies in normal and Duchenne muscular dystrophy dogs. These results will help guide translational AAV gene-therapy studies in dog models of muscular dystrophy.

摘要

腺相关病毒 (AAV)-6、8 和 9 是用于在犬模型中测试新型杜氏肌营养不良症基因治疗的有前途的基因传递载体。体液免疫对体内 AAV 转导有很大影响。然而,尚未系统检查正常和营养不良犬中针对 AAV-6、8 和 9 的中和抗体。为了获得针对 AAV-6、8 和 9 的抗体的血清流行率信息,我们使用体外转导抑制测定法测量了中和抗体滴度。我们检查了 72 份未接种疫苗的血清样本和 26 份接受过 AAV 基因转移的犬血清样本。我们的数据表明,AAV-6 中和抗体是最常见的抗体,无论犬的年龄、性别、疾病状况(是否营养不良)和先前细小病毒疫苗接种史如何。令人惊讶的是,在新生幼犬出生时就检测到高水平的抗 AAV-6 抗体。此外,在全身性 AAV 基因转移后,受影响但正常的新生犬会引起强烈的抗体反应。总之,我们的数据为正常和杜氏肌营养不良症犬中 AAV-6、8 和 9 中和抗体的血清流行率提供了重要的基线。这些结果将有助于指导肌肉营养不良犬模型中的转化 AAV 基因治疗研究。

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