CAF08 adjuvant enables single dose protection against respiratory syncytial virus infection in murine newborns.
Simon Daniel van HarenGabriel K PedersenAzad KumarTracy J RuckwardtSyed MoinIan N MooreMahnaz MinaiMark LiuJensen PakFrancesco BorrielloSimon Doss-GollinElisabeth M S BeijnenSaima AhmedMichaela HelmelPeter AndersenBarney S GrahamHanno SteenDennis ChristensenOfer LevyPublished in: Nature communications (2022)
Respiratory syncytial virus is a leading cause of morbidity and mortality in children, due in part to their distinct immune system, characterized by impaired induction of Th 1 immunity. Here we show application of cationic adjuvant formulation CAF08, a liposomal vaccine formulation tailored to induce Th 1 immunity in early life via synergistic engagement of Toll-like Receptor 7/8 and the C-type lectin receptor Mincle. We apply quantitative phosphoproteomics to human dendritic cells and reveal a role for Protein Kinase C-δ for enhanced Th1 cytokine production in neonatal dendritic cells and identify signaling events resulting in antigen cross-presentation. In a murine in vivo model a single immunization at birth with CAF08-adjuvanted RSV pre-fusion antigen protects newborn mice from RSV infection by induction of antigen-specific CD8 + T-cells and Th1 cells. Overall, we describe a pediatric adjuvant formulation and characterize its mechanism of action providing a promising avenue for development of early life vaccines against RSV and other respiratory viral pathogens.
Keyphrases
- respiratory syncytial virus
- early life
- dendritic cells
- toll like receptor
- immune response
- early stage
- drug delivery
- regulatory t cells
- nuclear factor
- protein kinase
- induced apoptosis
- endothelial cells
- inflammatory response
- gestational age
- sars cov
- cell cycle arrest
- high resolution
- social media
- cancer therapy
- pregnant women
- young adults
- type diabetes
- single cell
- genome wide
- induced pluripotent stem cells
- antimicrobial resistance
- cell death
- endoplasmic reticulum stress
- high fat diet induced
- gram negative
- dna methylation
- adipose tissue
- cord blood
- multidrug resistant
- cell proliferation
- preterm infants