Environmental and developmental factors shape anti-AAV immunity in pigs
Use of adeno-associated virus (AAV) vectors has revolutionized in vivo gene therapy, but the presence of pre-existing neutralizing antibodies remains a major barrier that can hinder clinical application. While large-animal models such as non-human primates have been used to study anti-AAV immunity, their high cost and limited accessibility present challenges for studying the impact of AAV immunity on AAV-based therapies. Here, we evaluate pigs as an immunologically relevant large-animal model for investigating humoral barriers to AAV-based gene therapy. Using ELISA-based profiling across 11 AAV serotypes, we detected immunoglobulin G (IgG) antibodies against AAV capsids in pigs as early as two weeks of age, with titers increasing with age and displaying serotype-specific dynamics. Animals maintained in standard housing displayed greater inter-individual variations and broader serotype-specific reactivities. Functional assays demonstrated that these antibodies neutralized AAV particles in a dose- and serotype-dependent manner, with IgG depletion restoring transduction in vitro. Sequence analysis indicated that capsid identity can partially predict cross-reactive binding, but only under controlled conditions. These findings establish pigs as a tunable model capable of recapitulating age- and environment-dependent features of anti-AAV immunity, providing a platform for studying humoral barriers and evaluating immune evasion strategies in AAV-based gene therapy.
Authors
- Godwin I. Iroanya
- Jonathan A. Green (ORCID: https://orcid.org/0000-0003-4968-8187)
- Ilangovan Raju
- Pradeep N. Subramanyam
- Kevin D. Wells
- Addison K. Byrne (ORCID: https://orcid.org/0009-0000-6329-0322)
- Chandra Boosani
Institutions
- University of Missouri (US)
Publication Details
- Journal
- Gene Therapy
- Published
- 2026-05-29
- DOI
- https://doi.org/10.1038/s41434-026-00625-1
- Primary Topic
- Virus-based gene therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Missouri
- National Institutes of Health
- NIH Office of the Director