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Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes

Treatment of monogenetic disorders using vectors based on adeno-associated virus (AAV) is an area of intense interest. AAV is non-pathogenic human virus, and preexisting capsid antibodies are prevalent in the population posing a challenge to the safety and efficacy of AAV-mediated gene therapies. In...

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Autores principales: West, Cara, Federspiel, Joel D., Rogers, Kara, Khatri, Arpana, Rao-Dayton, Sheila, Ocana, Mireia Fernandez, Lim, Sean, D'Antona, Aaron Michael, Casinghino, Sandra, Somanathan, Suryanarayan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282828/
https://www.ncbi.nlm.nih.gov/pubmed/37082966
http://dx.doi.org/10.1089/hum.2023.018
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author West, Cara
Federspiel, Joel D.
Rogers, Kara
Khatri, Arpana
Rao-Dayton, Sheila
Ocana, Mireia Fernandez
Lim, Sean
D'Antona, Aaron Michael
Casinghino, Sandra
Somanathan, Suryanarayan
author_facet West, Cara
Federspiel, Joel D.
Rogers, Kara
Khatri, Arpana
Rao-Dayton, Sheila
Ocana, Mireia Fernandez
Lim, Sean
D'Antona, Aaron Michael
Casinghino, Sandra
Somanathan, Suryanarayan
author_sort West, Cara
collection PubMed
description Treatment of monogenetic disorders using vectors based on adeno-associated virus (AAV) is an area of intense interest. AAV is non-pathogenic human virus, and preexisting capsid antibodies are prevalent in the population posing a challenge to the safety and efficacy of AAV-mediated gene therapies. In this study, we investigated the risk of AAV-mediated complement activation when sera from a cohort of human donors were exposed to AAV9 capsid. Seropositive donor sera carrying neutralizing antibodies from a previous environmental exposure activated complement when admixed with AAV9 capsids and complement activation was associated with donors who had higher levels of anti-AAV IgG1 antibodies. These findings were consistent with mass spectrometry analysis that identified increased binding of immunoglobulins and complement factors when AAV9 capsids were admixed with seropositive sera. Finally, complement activation was abrogated after IgG-depletion using affinity columns or serum pretreatment with an IgG degrading enzyme. Overall, these results demonstrate an important role of preexisting neutralizing antibodies in activating complement; a risk that can be mitigated by using adequate immunosuppression strategies when dosing seropositive patients with vector.
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spelling pubmed-102828282023-06-22 Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes West, Cara Federspiel, Joel D. Rogers, Kara Khatri, Arpana Rao-Dayton, Sheila Ocana, Mireia Fernandez Lim, Sean D'Antona, Aaron Michael Casinghino, Sandra Somanathan, Suryanarayan Hum Gene Ther Research Articles Treatment of monogenetic disorders using vectors based on adeno-associated virus (AAV) is an area of intense interest. AAV is non-pathogenic human virus, and preexisting capsid antibodies are prevalent in the population posing a challenge to the safety and efficacy of AAV-mediated gene therapies. In this study, we investigated the risk of AAV-mediated complement activation when sera from a cohort of human donors were exposed to AAV9 capsid. Seropositive donor sera carrying neutralizing antibodies from a previous environmental exposure activated complement when admixed with AAV9 capsids and complement activation was associated with donors who had higher levels of anti-AAV IgG1 antibodies. These findings were consistent with mass spectrometry analysis that identified increased binding of immunoglobulins and complement factors when AAV9 capsids were admixed with seropositive sera. Finally, complement activation was abrogated after IgG-depletion using affinity columns or serum pretreatment with an IgG degrading enzyme. Overall, these results demonstrate an important role of preexisting neutralizing antibodies in activating complement; a risk that can be mitigated by using adequate immunosuppression strategies when dosing seropositive patients with vector. Mary Ann Liebert, Inc., publishers 2023-06-01 2023-06-15 /pmc/articles/PMC10282828/ /pubmed/37082966 http://dx.doi.org/10.1089/hum.2023.018 Text en © Cara West et al. 2023; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
West, Cara
Federspiel, Joel D.
Rogers, Kara
Khatri, Arpana
Rao-Dayton, Sheila
Ocana, Mireia Fernandez
Lim, Sean
D'Antona, Aaron Michael
Casinghino, Sandra
Somanathan, Suryanarayan
Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title_full Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title_fullStr Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title_full_unstemmed Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title_short Complement Activation by Adeno-Associated Virus-Neutralizing Antibody Complexes
title_sort complement activation by adeno-associated virus-neutralizing antibody complexes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282828/
https://www.ncbi.nlm.nih.gov/pubmed/37082966
http://dx.doi.org/10.1089/hum.2023.018
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