Immune Toxicities in AAV Gene Therapy: Overview for Clinicians

Gene therapy using recombinant adeno-associated virus (rAAV) vectors has emerged as a transformative therapeutic modality for genetic disorders, demonstrating high transduction efficiency and a generally favorable safety profile during pre-clinical development. However, serious adverse events, including thrombotic microangiopathy, acute respiratory distress syndrome, hepatotoxicity, myocarditis, cytokine storm, and hemophagocytic lymphohistiocytosis, have been observed across multiple gene therapy clinical trials. Significant efforts have been made to understand the toxicities that cause these adverse events and clinical care for patients receiving gene therapies has evolved to mitigate their effects. These toxicities arise from a complex interplay between the innate and adaptive immune responses directed against the viral capsid and transgene products and are often compounded by pre-existing anti-AAV immunity. Immunomodulatory strategies have been developed to combat these responses to improve the long-term success of gene therapies, and this review provides clinicians managing gene therapy patients with an overview of mechanisms underlying AAV-associated immunotoxicities and a discussion of syndromes and mitigation strategies that have been reported in the clinical care of patients.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-03-31
DOI
https://doi.org/10.3390/ijms27073196
Primary Topic
Virus-based gene therapy research
Type
article
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0.00
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article

Immune Toxicities in AAV Gene Therapy: Overview for Clinicians

Shestruma Parajuli, Thomas Gallagher, Terence R. Flotte
International Journal of Molecular Sciences
Virus-based gene therapy research
article

Immune Toxicities in AAV Gene Therapy: Overview for Clinicians

Shestruma Parajuli, Thomas Gallagher, Terence R. Flotte
article en

Abstract

Gene therapy using recombinant adeno-associated virus (rAAV) vectors has emerged as a transformative therapeutic modality for genetic disorders, demonstrating high transduction efficiency and a generally favorable safety profile during pre-clinical development. However, serious adverse events, including thrombotic microangiopathy, acute respiratory distress syndrome, hepatotoxicity, myocarditis, cytokine storm, and hemophagocytic lymphohistiocytosis, have been observed across multiple gene therapy clinical trials. Significant efforts have been made to understand the toxicities that cause these adverse events and clinical care for patients receiving gene therapies has evolved to mitigate their effects. These toxicities arise from a complex interplay between the innate and adaptive immune responses directed against the viral capsid and transgene products and are often compounded by pre-existing anti-AAV immunity. Immunomodulatory strategies have been developed to combat these responses to improve the long-term success of gene therapies, and this review provides clinicians managing gene therapy patients with an overview of mechanisms underlying AAV-associated immunotoxicities and a discussion of syndromes and mitigation strategies that have been reported in the clinical care of patients.

International Journal of Molecular SciencesVol. 27(7)
University of Massachusetts Chan Medical School (US), Carilion Clinic (US), Virginia Tech (US)
Good health and well-being
Openalex Percentile: Top 23%
Virus-based gene therapy research
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