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Clinical enrollment assay to detect preexisting neutralizing antibodies to AAV6 with demonstrated transgene expression in gene therapy trials
by
Pan, Yonghua
, Lu, Yanmei
, Cao, Liching
, Meyer, Kathleen
, Ledeboer, Annemarie
in
Antibodies
/ Clinical trials
/ Expression vectors
/ Gene therapy
/ Gene transfer
/ Quality control
/ Serology
/ Transgenes
2023
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Clinical enrollment assay to detect preexisting neutralizing antibodies to AAV6 with demonstrated transgene expression in gene therapy trials
by
Pan, Yonghua
, Lu, Yanmei
, Cao, Liching
, Meyer, Kathleen
, Ledeboer, Annemarie
in
Antibodies
/ Clinical trials
/ Expression vectors
/ Gene therapy
/ Gene transfer
/ Quality control
/ Serology
/ Transgenes
2023
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Do you wish to request the book?
Clinical enrollment assay to detect preexisting neutralizing antibodies to AAV6 with demonstrated transgene expression in gene therapy trials
by
Pan, Yonghua
, Lu, Yanmei
, Cao, Liching
, Meyer, Kathleen
, Ledeboer, Annemarie
in
Antibodies
/ Clinical trials
/ Expression vectors
/ Gene therapy
/ Gene transfer
/ Quality control
/ Serology
/ Transgenes
2023
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Clinical enrollment assay to detect preexisting neutralizing antibodies to AAV6 with demonstrated transgene expression in gene therapy trials
Journal Article
Clinical enrollment assay to detect preexisting neutralizing antibodies to AAV6 with demonstrated transgene expression in gene therapy trials
2023
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Overview
Recombinant adeno-associated virus (AAV) vectors are the leading platform for gene delivery for a variety of clinical applications. Patients with preexisting antibodies to AAV are currently excluded from most AAV gene therapy trials to avoid vector neutralization and ensure response to therapy. Anti-AAV neutralizing antibodies (NAbs) are typically assessed by in vitro cell-based transduction inhibition (TI) assays. However, clinical relevance of the determined enrollment cutoff and the inherent variability of a cell-based assay present challenges for use as an enrollment screening test. Here, we describe an enrollment cutoff that was clinically validated and strategies to overcome assay challenges to enable long-term stable performance. A validated anti-AAV6 cell-based TI assay was used to support clinical enrollment across multiple investigational gene therapies and to evaluate AAV6 seroprevalence in healthy and disease populations. The clinical enrollment cutoff was determined statistically using samples collected from healthy donors, applying a 0.1% false error rate with the inclusion of a minimum significant ratio (MSR) metric and in consideration of results from in vivo mouse passive transfer studies. Our strategy for long-term monitoring and control of assay performance employed plate quality control samples flanking the predefined cutoff. An approach using donor samples was implemented to bridge different lots of critical reagents without the need to redefine the cutoff.
Publisher
Nature Publishing Group
Subject
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