腺相关病毒
血清型
遗传增强
病毒学
报告基因
效价
转基因
生物
衣壳
病毒
病毒载体
细胞
分子生物学
基因表达
载体(分子生物学)
遗传学
基因
重组DNA
作者
Ryota Watano,Kenji Ohba,Yoshihide Sehara,Yuka Hayashi,Yasushi Saga,Masashi Urabe,Tsukasa Ohmori,Hiroaki Mizukami
出处
期刊:Human Gene Therapy
[Mary Ann Liebert, Inc.]
日期:2025-05-19
卷期号:36 (11-12): 914-924
被引量:2
摘要
Gene therapy using adeno-associated virus (AAV) vectors is currently expanding to broad clinical applications. As the presence of a neutralizing antibody (NAb) against AAV capsids significantly restrains their efficacy, an accurate evaluation of NAb status is crucial for selecting appropriate candidates for gene therapy. Notably, cell-based NAb assays may not be sufficiently sensitive for detecting low-titer NAb, and few assays can evaluate multiple AAV serotypes using a commonly available cell. In this study, we developed a sensitive NAb assay against various AAV serotypes using commonly available HEK293 and Huh-7 cells. We found that adding glucose efficiently enhanced transgene expression across various AAV serotypes without causing cell damage. In addition, by combining a highly sensitive reporter gene, NanoLuc, the necessary dose of AAV vector was significantly reduced. The reduction of AAV dose resulted in the increased sensitivity of NAb detection as low as 100 vector genomes/cell. At the lower vector doses, sensitivity improvement was not observed regardless of serotypes, suggesting the limit of assay sensitivity of the cell-based NAb assay. These findings provide a highly sensitive methodology for assessing NAb titers and offer insights into conditions to attain maximal sensitivity in the cell-based NAb assay.
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