Evidence map›Paper›PMID 42901945›Full record

ArticleGene therapy2026

Prevalence of adeno-associated virus type 3B neutralizing antibodies in cohorts of healthy donors and Wilson's disease adults.

Céline Bouquet, Blanche Tamarit, Gloria Gonzalez Aseguinolaza, Veronica Ferrer, Sonia Valero, Anne Douar, Annelise Brossel, Rainard Fuhr, Jean-Philippe Combal

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Article in Gene therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Céline Bouquet *Vivet Therapeutics SAS, Paris, France.
Blanche Tamarit *Vivet Therapeutics SAS, Paris, France.
Gloria Gonzalez AseguinolazaDNA & RNA Medicine Division, Gene Therapy for Rare Diseases Department, Center for Applied Medical Research (CIMA), University of Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0002-1600-4562
Veronica FerrerVivet Therapeutics SAS, Paris, France.
Sonia ValeroVivet Therapeutics SAS, Paris, France.
Anne DouarVivet Therapeutics SAS, Paris, France.
Annelise BrosselVivet Therapeutics SAS, Paris, France.
Rainard FuhrParexel International GmbH, Berlin, Germany.
Jean-Philippe CombalVivet Therapeutics SAS, Paris, France. jpcombal@vivet-therapeutics.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adeno-associated virus (AAV) is widely used for liver-directed gene therapy, with AAV serotype 3B (AAV3B) showing particularly high tropism for human hepatocytes. However, pre-existing neutralizing antibodies (NAbs) against AAV represent a major barrier to efficient gene transfer and patient eligibility. We have recently demonstrated that subjects with intermediate NAb levels (1:5-1:45), that would be excluded from clinical trials, can be converted in eligible patients by the administration of IgG-cleaving enzymes. It is thus crucial to assess not only the seroprevalence but also titer distribution. Here, we analyzed anti-AAV3B NAb titers, using a validated cell-based transduction inhibition assay, in healthy adults and patients with Wilson's disease, a hepatic metabolic disorder amenable to AAV3B-mediated gene therapy. Two independent cohorts of healthy adults (n = 200 and n = 580) were analyzed; 33-36% of individuals were NAb positive, and prevalence increased with age. Differences were observed across ethnicities. Importantly, a substantial proportion of seropositive individuals (19%) exhibited intermediate NAb titers. In contrast, only 17.4% of Wilson's disease patients (n = 23) were positive, all with high NAb titers. These findings provide insights into target population eligibility, and titer distribution data support the potential of NAb-reduction approaches to expand access to systemic AAV3B-based gene therapies.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.