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A Novel Prophylaxis Strategy Using Liposomal Vaccine Adjuvant CAF09b Protects against Influenza Virus Disease.
Zimmermann, Julie; Schmidt, Signe Tandrup; Trebbien, Ramona; Cox, Rebecca Jane; Zhou, Fan; Follmann, Frank; Pedersen, Gabriel Kristian; Christensen, Dennis.
  • Zimmermann J; Center for Vaccine Research, Statens Serum Institut, 2300 Copenhagen S, Denmark.
  • Schmidt ST; Center for Vaccine Research, Statens Serum Institut, 2300 Copenhagen S, Denmark.
  • Trebbien R; Department of Virus and Microbiological Special Diagnostics, Statens Serum Institut, 2300 Copenhagen S, Denmark.
  • Cox RJ; Influenza Centre, Department of Clinical Science, University of Bergen, 5020 Bergen, Norway.
  • Zhou F; Influenza Centre, Department of Clinical Science, University of Bergen, 5020 Bergen, Norway.
  • Follmann F; Center for Vaccine Research, Statens Serum Institut, 2300 Copenhagen S, Denmark.
  • Pedersen GK; Center for Vaccine Research, Statens Serum Institut, 2300 Copenhagen S, Denmark.
  • Christensen D; Center for Vaccine Research, Statens Serum Institut, 2300 Copenhagen S, Denmark.
Int J Mol Sci ; 23(3)2022 Feb 06.
Article in English | MEDLINE | ID: covidwho-1674673
ABSTRACT
The SARS-CoV-2 pandemic caused a massive health and societal crisis, although the fast development of effective vaccines reduced some of the impact. To prepare for future respiratory virus pandemics, a pan-viral prophylaxis could be used to control the initial virus outbreak in the period prior to vaccine approval. The liposomal vaccine adjuvant CAF®09b contains the TLR3 agonist polyinosinicpolycytidylic acid, which induces a type I interferon (IFN-I) response and an antiviral state in the affected tissues. When testing CAF09b liposomes as a potential pan-viral prophylaxis, we observed that intranasal administration of CAF09b liposomes to mice resulted in an influx of innate immune cells into the nose and lungs and upregulation of IFN-I-related gene expression. When CAF09b liposomes were administered prior to challenge with mouse-adapted influenza A/Puerto Rico/8/1934 virus, it protected from severe disease, although the virus was still detectable in the lungs. However, when CAF09b liposomes were administered after influenza challenge, the mice had a similar disease course to controls. In conclusion, CAF09b may be a suitable candidate as a pan-viral prophylactic treatment for epidemic viruses, but must be administered prior to virus exposure to be effective.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza Vaccines / Orthomyxoviridae Infections / Influenza, Human / Vaccine Development / Adjuvants, Vaccine Type of study: Prognostic study Topics: Vaccines Limits: Animals / Humans Language: English Year: 2022 Document Type: Article Affiliation country: Ijms23031850

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza Vaccines / Orthomyxoviridae Infections / Influenza, Human / Vaccine Development / Adjuvants, Vaccine Type of study: Prognostic study Topics: Vaccines Limits: Animals / Humans Language: English Year: 2022 Document Type: Article Affiliation country: Ijms23031850