Rapid AAV-Neutralizing Antibody Determination with a Cell-Binding Assay
Genre
Journal articleDate
2019-01-02Author
Guo, PingZhang, Junping
Chrzanowski, Matthew
Huang, Jianhe
Chew, Helen
Firrman, Jenni
Sang, Nianli
Diao, Yong
XIAO, WEIDONG
Group
Sol Sherry Thrombosis Research Center (Temple University)Cardiovascular Research Center (Temple University)
Department
Microbiology and ImmunologyClinical Sciences
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http://hdl.handle.net/20.500.12613/8785
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https://doi.org/10.1016/j.omtm.2018.11.007Abstract
Recombinant adeno-associated virus (rAAV) has been developed as a successful vector for both basic research and human gene therapy. However, neutralizing antibodies (NAbs) against AAV capsids can abolish AAV infectivity on target cells, reducing the transduction efficacy. Absence of AAV NAb has become a prerequisite qualification for patients enrolled in gene therapy trials. Nevertheless, accurate assessment of AAV NAb has remained a challenging task. Here we developed a rapid assay based on the observations that AAV NAb inhibits rAAV binding to the host cell surface and NAb titers are negatively related to the amount of AAV genomes binding to the target cells. By quantifying the AAV genome on the target cells in the presence of anti-sera, AAV NAb titers can be accurately determined. The titer determined by this assay correlates well with the classical transduction-based assays. A major advantage of this method is that it can be carried out with a 30-min binding assay without the lengthy wait for a transduction outcome. This assay is independent of transduction performance of AAV serotype in the target cells. Therefore, the AAV cell-binding assay for NAb determination offers an alternative method for in vivo NAb assay.Citation to related work
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Molecular Therapy - Methods and Clinical Development, Vol. 13ADA compliance
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http://dx.doi.org/10.34944/dspace/8749
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