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在腺相关病毒(AAV)基因转移治疗前检测预先存在的抗体:原理、经验教训及未来考量

Testing preexisting antibodies prior to AAV gene transfer therapy: rationale, lessons and future considerations.

作者信息

Mendell Jerry R, Connolly Anne M, Lehman Kelly J, Griffin Danielle A, Khan Sohrab Z, Dharia Sachi D, Quintana-Gallardo Lucía, Rodino-Klapac Louise R

机构信息

Center for Gene Therapy, The Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.

Department of Pediatrics and Neurology, The Ohio State University, Columbus, OH 43205, USA.

出版信息

Mol Ther Methods Clin Dev. 2022 Feb 26;25:74-83. doi: 10.1016/j.omtm.2022.02.011. eCollection 2022 Jun 9.

DOI:10.1016/j.omtm.2022.02.011
PMID:35356756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8933338/
Abstract

Given the increasing number of gene transfer therapy studies either completed or underway, there is growing attention to the importance of preexisting adaptive immunity to the viral vectors used. The recombinant viral vectors developed for gene transfer therapy share structural features with naturally occurring wild-type virus. Antibodies generated against viral vectors obtained through a previous exposure to wild-type virus can potentially compromise transgene expression by blocking transduction, thereby limiting the therapeutic efficacy of the gene transfer therapy; they may also pose potential safety concerns. Therefore, systemic gene transfer delivery requires testing patients for preexisting antibodies. Two different assays have been used: (1) binding assays that focus on total antibodies (both neutralizing and non-neutralizing) and (2) neutralizing assays that detect neutralizing antibodies. In this review we focus on adeno-associated virus-based gene therapies, describing the immune response that occurs to naturally occurring adeno-associated viruses, the implications for patients with this exposure, the assays used to detect preexisting immune responses, and strategies to circumvent preexisting adaptive immunity to expand the patient base that could benefit from such therapies.

摘要

鉴于已完成或正在进行的基因转移治疗研究数量不断增加,人们越来越关注对所用病毒载体预先存在的适应性免疫的重要性。为基因转移治疗开发的重组病毒载体与天然存在的野生型病毒具有共同的结构特征。通过先前接触野生型病毒而产生的针对病毒载体的抗体可能会通过阻断转导来潜在地损害转基因表达,从而限制基因转移治疗的疗效;它们还可能引发潜在的安全问题。因此,全身性基因转移递送需要检测患者是否预先存在抗体。已经使用了两种不同的检测方法:(1)侧重于总抗体(包括中和抗体和非中和抗体)的结合检测,以及(2)检测中和抗体的中和检测。在本综述中,我们重点关注基于腺相关病毒的基因治疗,描述对天然存在的腺相关病毒产生的免疫反应、这种接触对患者的影响、用于检测预先存在的免疫反应的检测方法,以及规避预先存在的适应性免疫以扩大可从此类治疗中受益的患者群体的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/920002395f57/gr6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/d6c09ae58e4a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/795c002adac0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/275224ac848e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/d67119a3761c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/a3f8616c6e18/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/920002395f57/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/64158377b949/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/d6c09ae58e4a/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/795c002adac0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/275224ac848e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/d67119a3761c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/a3f8616c6e18/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc46/8933338/920002395f57/gr6.jpg

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