Influenza viruses cause a common respiratory disease known as influenza. In humans, seasonal influenza viruses can lead to epidemics, with avian influenza viruses of particular concern because they can infect multiple species and lead to unpredictable and severe disease. Therefore, there is an urgent need for a universal influenza vaccine that provides protection against seasonal and pre-pandemic influenza virus strains. The cyclic GMP-AMP (cGAMP) is a promising adjuvant for subunit vaccines that promotes type I interferons production through the stimulator of interferon genes (STING) pathway. The encapsulation of cGAMP in acetalated dextran (Ace-DEX) microparticles (MPs) enhances its intracellular delivery. In this study, the Computationally Optimized Broadly Reactive Antigen (COBRA) methodology was used to generate H1, H3, and H5 vaccine candidates. Monovalent and multivalent COBRA HA vaccines formulated with cGAMP Ace-DEX MPs were evaluated in a mouse model for antibody responses and protection against viral challenge. Serological analysis showed that cGAMP MPs adjuvanted monovalent and multivalent COBRA vaccines elicited robust antigen-specific antibody responses after a prime-boost vaccination and antibody titers were further enhanced after second boost. Compared to COBRA vaccine groups with no adjuvant or blank MPs, the cGAMP MPs enhanced HAI antibody responses against COBRA vaccination. The HAI antibody titers were not significantly different between cGAMP MPs adjuvanted monovalent and multivalent COBRA vaccine groups for most of the viruses tested in panels. The cGAMP MPs adjuvanted COBRA vaccines groups had higher antigen-specific IgG2a binding titers than the COBRA vaccine groups with no adjuvant or blank MPs. The COBRA vaccines formulated with cGAMP MPs mitigated disease caused by influenza viral challenge and decreased pulmonary viral titers in mice. Therefore, the formulation of COBRA vaccines plus cGAMP MPs is a promising universal influenza vaccine that elicits protective immune responses against human seasonal and pre-pandemic strains.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10925245PMC
http://dx.doi.org/10.1101/2024.02.27.582355DOI Listing

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  • Seasonal influenza viruses lead to epidemics in humans, while avian influenza poses a serious risk due to its ability to infect multiple species and cause severe illness, highlighting the need for a universal vaccine.
  • The study explores using cGAMP, an adjuvant that boosts immune response through the STING pathway, encapsulated in Ace-DEX microparticles to enhance vaccine efficacy; specifically, it evaluates COBRA vaccine candidates in mice.
  • The results showed that cGAMP-adjuvanted COBRA vaccines provoked strong immune responses, including higher specific antibodies and reduced viral impact, proving their potential as a universal influenza vaccine for both seasonal and pre-pandemic strains.
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Influenza viruses cause a common respiratory disease known as influenza. In humans, seasonal influenza viruses can lead to epidemics, with avian influenza viruses of particular concern because they can infect multiple species and lead to unpredictable and severe disease. Therefore, there is an urgent need for a universal influenza vaccine that provides protection against seasonal and pre-pandemic influenza virus strains.

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  • Subunit-based vaccines offer quicker production but often need adjuvants like MF59, which primarily generates a helper T-cell type 2 (Th2) immune response, less optimal for strong protection against influenza.
  • A study used acetalated dextran (Ace-DEX) to create microparticles that effectively encapsulate the Th1-stimulating adjuvant cGAMP, demonstrating that these particles provide stronger immune responses compared to conventional adjuvants in mice.
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