npj Vaccines · 2023 · 21 citations · 49 references
Veterinary MedicineImmunologyInfectious DiseasesImmunizationVaccine ImmunologyVaccinologyConjugate VaccinesMaternal ImmunizationVaccinationVaccine DeliveryVaccine FormulationVirus-like Particle VaccinesAntibodiesBacterial Vaccine AntigensCapsular PolysaccharidesMaternal Vaccine ImmunityMultivalent Vaccine FormulationsNanoparticle Vaccine FormulationsPolysaccharide VaccinesVirus-like Particles
A maternal vaccine to protect neonates against Group B Streptococcus invasive infection is an unmet medical need. Such a vaccine should ideally be offered during the third trimester of pregnancy and induce strong immune responses after a single dose to maximize the time for placental transfer of protective antibodies. A key target antigen is the capsular polysaccharide, an anti-phagocytic virulence factor that elicits protective antibodies when conjugated to carrier proteins. The most prevalent polysaccharide serotypes conjugated to tetanus or diphtheria toxoids have been tested in humans as monovalent and multivalent formulations, showing excellent safety profiles and immunogenicity. However, responses were suboptimal in unprimed individuals after a single shot, the ideal schedule for vaccination during the third trimester of pregnancy. In the present study, we obtained and optimized self-assembling virus-like particles conjugated to Group B Streptococcus capsular polysaccharides. The resulting glyco-nanoparticles elicited strong immune responses in mice already after one immunization, providing pre-clinical proof of concept for a single-dose vaccine.
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Species-Specific Recognition of Single-Stranded RNA via Toll-like Receptor 7 and 8
Florian Heil, Hiroaki Hemmi, Hubertus Hochrein et al. · Science · 2004 · 3.9K citations
Self-assembling influenza nanoparticle vaccines elicit broadly neutralizing H1N1 antibodies
Masaru Kanekiyo, Chih‐Jen Wei, Hadi M. Yassine et al. · Nature · 2013 · 903 citations · Full text