rAAV expressing a COBRA-designed influenza hemagglutinin generates a protective and durable adaptive immune response with a single dose.

adeno-associated virus influenza vaccines

Journal

Journal of virology
ISSN: 1098-5514
Titre abrégé: J Virol
Pays: United States
ID NLM: 0113724

Informations de publication

Date de publication:
30 Jul 2024
Historique:
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 30 7 2024
Statut: aheadofprint

Résumé

Influenza remains a worldwide public health threat. Although seasonal influenza vaccines are currently the best means of preventing severe disease, the standard-of-care vaccines require frequent updating due to antigenic drift and can have low efficacy, particularly in vulnerable populations. Here, we demonstrate that a single administration of a recombinant adenovirus-associated virus (rAAV) vector expressing a computationally optimized broadly reactive antigen (COBRA)-derived influenza H1 hemagglutinin (HA) induces strongly neutralizing and broadly protective antibodies in naïve mice and ferrets with pre-existing influenza immunity. Following a lethal viral challenge, the rAAV-COBRA vaccine allowed for significantly reduced viral loads in the upper and lower respiratory tracts and complete protection from morbidity and mortality that lasted for at least 5 months post-vaccination. We observed no signs of antibody waning during this study. CpG motif enrichment of the antigen can act as an internal adjuvant to further enhance the immune responses to allow for lower vaccine dosages with the induction of unique interferon-producing CD4+ and CD8+ T cells specific to HA head and stem peptide sequences. Our studies highlight the utility of rAAV as an effective platform to improve seasonal influenza vaccines. Developing an improved seasonal influenza vaccine remains an ambitious goal of researchers and clinicians alike. With influenza routinely causing severe epidemics with the potential to rise to pandemic levels, it is critical to create an effective, broadly protective, and durable vaccine to improve public health worldwide. As a potential solution, we created a rAAV viral vector expressing a COBRA-optimized influenza hemagglutinin antigen with modestly enriched CpG motifs to evoke a robust and long-lasting immune response after a single intramuscular dose without needing boosts or adjuvants. Importantly, the rAAV vaccine boosted antibody breadth to future strains in ferrets with pre-existing influenza immunity. Together, our data support further investigation into the utility of viral vectors as a potential avenue to improve our seasonal influenza vaccines.

Identifiants

pubmed: 39078191
doi: 10.1128/jvi.00781-24
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0078124

Auteurs

Kristin B Wiggins (KB)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Stephen M Winston (SM)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Isaiah L Reeves (IL)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Jessica Gaevert (J)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Yunyu Spence (Y)

Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Mark A Brimble (MA)

Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Brandi Livingston (B)

Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Christopher L Morton (CL)

Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Paul G Thomas (PG)

Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Andrea J Sant (AJ)

David H. Smith Center for Vaccine Biology and Immunology, Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York, USA.

Ted M Ross (TM)

Department of Infectious Biology, Cleveland Clinic, Cleveland, Ohio, USA.
Cleveland Clinic, Florida Research and Innovation Center, Port St. Lucie, Florida, USA.

Andrew M Davidoff (AM)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Stacey Schultz-Cherry (S)

St. Jude Graduate School of Biomedical Sciences, Memphis, Tennessee, USA.
Department of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Classifications MeSH