检测生物相关的低滴度中和抗体对抗腺相关病毒需要敏感的体外检测。

Q1 Immunology and Microbiology Human Gene Therapy Methods Pub Date : 2019-04-01 Epub Date: 2019-03-29 DOI:10.1089/hgtb.2018.263
Anita Kruzik, Herwig Koppensteiner, Damir Fetahagic, Bettina Hartlieb, Sebastian Dorn, Stefan Romeder-Finger, Sogue Coulibaly, Alfred Weber, Werner Hoellriegl, Frank M Horling, Friedrich Scheiflinger, Birgit M Reipert, Maurus de la Rosa
{"title":"检测生物相关的低滴度中和抗体对抗腺相关病毒需要敏感的体外检测。","authors":"Anita Kruzik,&nbsp;Herwig Koppensteiner,&nbsp;Damir Fetahagic,&nbsp;Bettina Hartlieb,&nbsp;Sebastian Dorn,&nbsp;Stefan Romeder-Finger,&nbsp;Sogue Coulibaly,&nbsp;Alfred Weber,&nbsp;Werner Hoellriegl,&nbsp;Frank M Horling,&nbsp;Friedrich Scheiflinger,&nbsp;Birgit M Reipert,&nbsp;Maurus de la Rosa","doi":"10.1089/hgtb.2018.263","DOIUrl":null,"url":null,"abstract":"<p><p>Patients with preexisting anti-adeno-associated virus serotype 8 (AAV8) neutralizing antibodies (NAbs) are currently excluded from AAV8 gene therapy trials. Therefore, the assessment of biologically relevant AAV8-NAb titers is critical for product development in gene therapy. However, standardized assays have not been routinely used to determine anti-AAV8-NAb titers, contributing to a wide range of reported anti-AAV8 prevalence rates. Using a clinical <i>in vitro</i> NAb assay in a separate study, a higher than expected anti-AAV8-NAb prevalence of about 50% was found in international cohorts. This comparative study has a translational character, confirming the biological relevance of anti-AAV8-antibody titers measured by this assay. The significance of low-titer anti-AAV8 NAbs is shown, along with the relevance of the <i>in vitro</i> assay cutoff (1:5) compared with other assays. Importantly, internally standardized reagents and purified AAV8 constructs containing 90% full capsids were used to reduce the effect of empty capsids. It was found that even very low anti-AAV8-NAb titers (<1:5) could efficiently hinder transduction <i>in vivo</i>, demonstrating the importance of sensitive NAb assays for clinical applications. The <i>in vitro</i> NAb assay was found to be more sensitive than an <i>in vivo</i> NAb assay and thus more suitable for patient screening. Additionally, the study showed that anti-AAV8-NAb titers <1:5 were very rare, further supporting the <i>in vitro</i> assay. However, assays using a lower cutoff may still be useful to explain potential variances in transgene expression. These findings support the relevance of the higher than expected prevalence of anti-AAV8 NAbs, highlighting the need for strategies to circumvent preexisting anti-AAV8 NAbs.</p>","PeriodicalId":13126,"journal":{"name":"Human Gene Therapy Methods","volume":"30 2","pages":"35-43"},"PeriodicalIF":0.0000,"publicationDate":"2019-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/hgtb.2018.263","citationCount":"18","resultStr":"{\"title\":\"Detection of Biologically Relevant Low-Titer Neutralizing Antibodies Against Adeno-Associated Virus Require Sensitive <i>In Vitro</i> Assays.\",\"authors\":\"Anita Kruzik,&nbsp;Herwig Koppensteiner,&nbsp;Damir Fetahagic,&nbsp;Bettina Hartlieb,&nbsp;Sebastian Dorn,&nbsp;Stefan Romeder-Finger,&nbsp;Sogue Coulibaly,&nbsp;Alfred Weber,&nbsp;Werner Hoellriegl,&nbsp;Frank M Horling,&nbsp;Friedrich Scheiflinger,&nbsp;Birgit M Reipert,&nbsp;Maurus de la Rosa\",\"doi\":\"10.1089/hgtb.2018.263\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Patients with preexisting anti-adeno-associated virus serotype 8 (AAV8) neutralizing antibodies (NAbs) are currently excluded from AAV8 gene therapy trials. Therefore, the assessment of biologically relevant AAV8-NAb titers is critical for product development in gene therapy. However, standardized assays have not been routinely used to determine anti-AAV8-NAb titers, contributing to a wide range of reported anti-AAV8 prevalence rates. Using a clinical <i>in vitro</i> NAb assay in a separate study, a higher than expected anti-AAV8-NAb prevalence of about 50% was found in international cohorts. This comparative study has a translational character, confirming the biological relevance of anti-AAV8-antibody titers measured by this assay. The significance of low-titer anti-AAV8 NAbs is shown, along with the relevance of the <i>in vitro</i> assay cutoff (1:5) compared with other assays. Importantly, internally standardized reagents and purified AAV8 constructs containing 90% full capsids were used to reduce the effect of empty capsids. It was found that even very low anti-AAV8-NAb titers (<1:5) could efficiently hinder transduction <i>in vivo</i>, demonstrating the importance of sensitive NAb assays for clinical applications. The <i>in vitro</i> NAb assay was found to be more sensitive than an <i>in vivo</i> NAb assay and thus more suitable for patient screening. Additionally, the study showed that anti-AAV8-NAb titers <1:5 were very rare, further supporting the <i>in vitro</i> assay. However, assays using a lower cutoff may still be useful to explain potential variances in transgene expression. These findings support the relevance of the higher than expected prevalence of anti-AAV8 NAbs, highlighting the need for strategies to circumvent preexisting anti-AAV8 NAbs.</p>\",\"PeriodicalId\":13126,\"journal\":{\"name\":\"Human Gene Therapy Methods\",\"volume\":\"30 2\",\"pages\":\"35-43\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1089/hgtb.2018.263\",\"citationCount\":\"18\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Gene Therapy Methods\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1089/hgtb.2018.263\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/3/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Gene Therapy Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/hgtb.2018.263","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/3/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 18

摘要

先前存在抗腺相关病毒血清型8 (AAV8)中和抗体(nab)的患者目前被排除在AAV8基因治疗试验之外。因此,评估生物学相关的AAV8-NAb滴度对于基因治疗的产品开发至关重要。然而,标准化检测尚未常规用于测定抗aav8 - nab滴度,这导致了广泛的抗aav8患病率报告。在另一项研究中使用临床体外NAb测定,在国际队列中发现抗aav8 -NAb患病率高于预期,约为50%。该比较研究具有翻译特性,证实了该试验测定的抗aav8抗体滴度的生物学相关性。低效价抗aav8抗体的重要性,以及与其他检测方法相比体外检测截止值(1:5)的相关性。重要的是,使用内部标准化试剂和含有90%完整衣壳的纯化AAV8构建物来减少空衣壳的影响。研究发现,即使体内抗aav8 -NAb滴度非常低,也证明了敏感的NAb检测对临床应用的重要性。体外NAb测定被发现比体内NAb测定更敏感,因此更适合于患者筛选。此外,研究显示抗aav8 - nab的体外滴度测定。然而,使用较低截止值的检测可能仍然有助于解释转基因表达的潜在差异。这些发现支持了抗aav8抗体高于预期患病率的相关性,强调了规避先前存在的抗aav8抗体的策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Detection of Biologically Relevant Low-Titer Neutralizing Antibodies Against Adeno-Associated Virus Require Sensitive In Vitro Assays.

Patients with preexisting anti-adeno-associated virus serotype 8 (AAV8) neutralizing antibodies (NAbs) are currently excluded from AAV8 gene therapy trials. Therefore, the assessment of biologically relevant AAV8-NAb titers is critical for product development in gene therapy. However, standardized assays have not been routinely used to determine anti-AAV8-NAb titers, contributing to a wide range of reported anti-AAV8 prevalence rates. Using a clinical in vitro NAb assay in a separate study, a higher than expected anti-AAV8-NAb prevalence of about 50% was found in international cohorts. This comparative study has a translational character, confirming the biological relevance of anti-AAV8-antibody titers measured by this assay. The significance of low-titer anti-AAV8 NAbs is shown, along with the relevance of the in vitro assay cutoff (1:5) compared with other assays. Importantly, internally standardized reagents and purified AAV8 constructs containing 90% full capsids were used to reduce the effect of empty capsids. It was found that even very low anti-AAV8-NAb titers (<1:5) could efficiently hinder transduction in vivo, demonstrating the importance of sensitive NAb assays for clinical applications. The in vitro NAb assay was found to be more sensitive than an in vivo NAb assay and thus more suitable for patient screening. Additionally, the study showed that anti-AAV8-NAb titers <1:5 were very rare, further supporting the in vitro assay. However, assays using a lower cutoff may still be useful to explain potential variances in transgene expression. These findings support the relevance of the higher than expected prevalence of anti-AAV8 NAbs, highlighting the need for strategies to circumvent preexisting anti-AAV8 NAbs.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Human Gene Therapy Methods
Human Gene Therapy Methods BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases. The Journal is divided into three parts. Human Gene Therapy, the flagship, is published 12 times per year. HGT Methods, a bimonthly journal, focuses on the applications of gene therapy to product testing and development. HGT Clinical Development, a quarterly journal, serves as a venue for publishing data relevant to the regulatory review and commercial development of cell and gene therapy products.
期刊最新文献
Lot-to-Lot Variation in Adeno-Associated Virus Serotype 9 (AAV9) Preparations. Fast-Seq: A Simple Method for Rapid and Inexpensive Validation of Packaged Single-Stranded Adeno-Associated Viral Genomes in Academic Settings. LINC00958 Accelerates Cell Proliferation and Migration in Non-Small Cell Lung Cancer Through JNK/c-JUN Signaling. Nanoparticle Tracking of Adenovirus by Light Scattering and Fluorescence Detection. LINC00958 accelerates cell proliferation and migration in non-small cell lung cancer through JNK/c-JUN signaling.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1