Long-term protective potency of AAV vector-based SARS-CoV-2 prophylaxis in mice and non-human primates - Report - MDSpire

Long-term protective potency of AAV vector-based SARS-CoV-2 prophylaxis in mice and non-human primates

  • By

  • Ekaterina I. Ryabova

  • Artem A. Derkaev

  • Ilias B. Esmagambetov

  • Mikhail A. Dovgiy

  • Ilya V. Gordeychuk

  • Inna V. Shuliakova

  • Rosa M. Hossain

  • Anton A. Blinov

  • Anna A. Iliukhina

  • Daria M. Grousova

  • Ilya D. Zorkov

  • Daria V. Avdoshina

  • Stanislav A. Gulyaev

  • Vasiliy D. Apolokhov

  • Tatiana V. Gulyaeva

  • Irina A. Favorskaya

  • Dmitry V. Shcheblyakov

  • Alexander L. Gintsburg

  • Denis Y. Logunov

  • June 4, 2026

  • 0 min

Share

Clinical Report: Sustained Efficacy of AAV Vector-Based SARS-CoV-2 Prevention

Overview

This study evaluates the long-term efficacy of an rAAV vector delivering the P2C5-Fc antibody in murine models and common marmosets. Results indicate sustained antibody expression and protective efficacy against SARS-CoV-2 variants for over a year.

Background

The COVID-19 pandemic has highlighted the need for effective preventive strategies against SARS-CoV-2, particularly for high-risk populations. Traditional vaccines may not provide adequate protection due to rapid viral evolution and immune evasion. rAAV-mediated delivery of neutralizing antibodies offers a promising alternative for long-term prophylaxis.

Data Highlights

SpeciesPeak Antibody Detection (Days)Duration of Protective Levels (Days)
Mice120480+
Marmosets1201120

Key Findings

  • Single intramuscular injection of rAAV-P2C5-Fc resulted in rapid antibody production.
  • Peak serum concentrations were reached by approximately 120 days.
  • Neutralizing titers provided complete protection against lethal SARS-CoV-2 challenges for up to 460 days in mice.
  • Biodistribution showed minimal off-target spread, with predominant localization at the injection site and lymph nodes.
  • Moderate anti-AAV capsid antibody responses were detected, while anti-drug antibodies against P2C5-Fc remained undetectable.

Clinical Implications

The findings suggest that rAAV vectors could serve as a viable option for long-term SARS-CoV-2 prophylaxis, particularly in immunocompromised populations. Further studies are needed to evaluate the safety and efficacy in human subjects.

Conclusion

This study supports the potential of rAAV-mediated antibody delivery as a durable immunoprophylaxis strategy against SARS-CoV-2, warranting further investigation in clinical settings.

Related Resources & Content

  1. The Journal of Infectious Diseases, 2023 -- Analysis of Mouse-Adapted Marburg and Ravn Viruses in BALB/c and CD-1 Mouse Models
  2. The Journal of Infectious Diseases, 2023 -- Development of a Cynomolgus Macaque Model for Investigating Respiratory Illness Induced by Human Adenovirus Type 55
  3. The Journal of Infectious Diseases, 2023 -- Weekly Administration of MK-8527 Provides Protection Against Intrarectal SHIV Exposure in Rhesus Macaques
  4. Archives of Toxicology, 2024 -- An Overview of Experimental Toxicity Research on COVID-19 Vaccines: Insights from Toxicology Journals
  5. COVID-19 Treatment Clinical Care for Outpatients | Covid | CDC, 2026
  6. Vectored long-term co-delivery of antibodies for SARS-CoV-2, RSV and Influenza prophylaxis - ScienceDirect, 2025
  7. COVID-19 Treatment Clinical Care for Outpatients | Covid | CDC
  8. Vectored long-term co-delivery of antibodies for SARS-CoV-2, RSV and Influenza prophylaxis - ScienceDirect

Original Source(s)

Related Content