Limitation of Assay Sensitivity Revealed by the Improvement of Cell-Based Assay Against Various Adeno-Associated Virus Serotypes

被引:0
作者
Watano, Ryota [1 ]
Ohba, Kenji [1 ]
Sehara, Yoshihide [1 ]
Hayashi, Yuka [1 ,2 ]
Saga, Yasushi [1 ,3 ]
Urabe, Masashi [1 ]
Ohmori, Tsukasa [4 ]
Mizukami, Hiroaki [1 ]
机构
[1] Jichi Med Univ, Ctr Mol Med, Div Genet Therapeut, 3311-1 Yakushiji, Shimotsuke, Tochigi 3290498, Japan
[2] Jichi Med Univ, Saitama Med Ctr, Dept Neurol, Saitama, Japan
[3] Jichi Med Univ, Dept Obstet & Gynecol, Shimotsuke, Japan
[4] Jichi Med Univ, Sch Med, Dept Biochem, Shimotsuke, Japan
基金
日本学术振兴会;
关键词
adeno-associated virus vector; gene therapy; neutralizing antibody; cell-based assay; NEUTRALIZING ANTIBODIES; HUMORAL IMMUNITY; GENE-TRANSFER; PREVALENCE; EXPRESSION; DELIVERY; VECTORS;
D O I
10.1089/hum.2024.261
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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.
引用
收藏
页码:914 / 924
页数:11
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