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Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy

Onasemnogene abeparvovec is a recombinant adeno-associated virus serotype 9 (AAV9) vector-based gene therapy for spinal muscular atrophy (SMA). Patients with elevated titers of anti-AAV9 antibodies (AAV9-Ab) should not receive onasemnogene abeparvovec because of potential safety and efficacy implica...

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Autores principales: Day, John W., Mendell, Jerry R., Burghes, Arthur H.M., van Olden, Rudolf W., Adhikary, Rishi R., Dilly, Keith W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562739/
https://www.ncbi.nlm.nih.gov/pubmed/37822718
http://dx.doi.org/10.1016/j.omtm.2023.101117
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author Day, John W.
Mendell, Jerry R.
Burghes, Arthur H.M.
van Olden, Rudolf W.
Adhikary, Rishi R.
Dilly, Keith W.
author_facet Day, John W.
Mendell, Jerry R.
Burghes, Arthur H.M.
van Olden, Rudolf W.
Adhikary, Rishi R.
Dilly, Keith W.
author_sort Day, John W.
collection PubMed
description Onasemnogene abeparvovec is a recombinant adeno-associated virus serotype 9 (AAV9) vector-based gene therapy for spinal muscular atrophy (SMA). Patients with elevated titers of anti-AAV9 antibodies (AAV9-Ab) should not receive onasemnogene abeparvovec because of potential safety and efficacy implications. We conducted a retrospective study to describe the seroprevalence of anti-AAV9 binding antibodies for pediatric patients with SMA in the United States. At initial testing, 13.0% (115 of 882) of patients (mean [SD] age, 26.29 [33.66] weeks) had elevated AAV9-Ab titers. The prevalence of elevated titers decreased as age increased, with 18.2% (92 of 507) of patients ≤3 months old but only 1.1% (1 of 92) of patients ≥21 months old having elevated titers. This suggests transplacental maternal transfer of antibodies. No patterns of geographic variations in AAV9-Ab prevalence were confirmed. Elevated AAV9-Ab titers in children <6 weeks old decreased in all circumstances. Lower magnitudes of elevated titers declined more rapidly than greater magnitudes. Retesting was completed at the discretion of the treating clinician, so age at testing and time between tests varied. AAV9-Ab retesting should be considered when patients have elevated titers, and elevations at a young age are not a deterrent to eventual onasemnogene abeparvovec administration. Early disease-modifying treatment for SMA leads to optimal outcomes.
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spelling pubmed-105627392023-10-11 Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy Day, John W. Mendell, Jerry R. Burghes, Arthur H.M. van Olden, Rudolf W. Adhikary, Rishi R. Dilly, Keith W. Mol Ther Methods Clin Dev Original Article Onasemnogene abeparvovec is a recombinant adeno-associated virus serotype 9 (AAV9) vector-based gene therapy for spinal muscular atrophy (SMA). Patients with elevated titers of anti-AAV9 antibodies (AAV9-Ab) should not receive onasemnogene abeparvovec because of potential safety and efficacy implications. We conducted a retrospective study to describe the seroprevalence of anti-AAV9 binding antibodies for pediatric patients with SMA in the United States. At initial testing, 13.0% (115 of 882) of patients (mean [SD] age, 26.29 [33.66] weeks) had elevated AAV9-Ab titers. The prevalence of elevated titers decreased as age increased, with 18.2% (92 of 507) of patients ≤3 months old but only 1.1% (1 of 92) of patients ≥21 months old having elevated titers. This suggests transplacental maternal transfer of antibodies. No patterns of geographic variations in AAV9-Ab prevalence were confirmed. Elevated AAV9-Ab titers in children <6 weeks old decreased in all circumstances. Lower magnitudes of elevated titers declined more rapidly than greater magnitudes. Retesting was completed at the discretion of the treating clinician, so age at testing and time between tests varied. AAV9-Ab retesting should be considered when patients have elevated titers, and elevations at a young age are not a deterrent to eventual onasemnogene abeparvovec administration. Early disease-modifying treatment for SMA leads to optimal outcomes. American Society of Gene & Cell Therapy 2023-09-20 /pmc/articles/PMC10562739/ /pubmed/37822718 http://dx.doi.org/10.1016/j.omtm.2023.101117 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Day, John W.
Mendell, Jerry R.
Burghes, Arthur H.M.
van Olden, Rudolf W.
Adhikary, Rishi R.
Dilly, Keith W.
Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title_full Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title_fullStr Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title_full_unstemmed Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title_short Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy
title_sort adeno-associated virus serotype 9 antibody seroprevalence for patients in the united states with spinal muscular atrophy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562739/
https://www.ncbi.nlm.nih.gov/pubmed/37822718
http://dx.doi.org/10.1016/j.omtm.2023.101117
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