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DS2 designer pre-fusion F vaccine induces strong and protective antibody response against RSV infection.

NPJ Vaccines

December 2024

Comprehensive AIDS Research Center, Pandemic Research Alliance Unit, Center for Infection Biology, School of Basic Medical Sciences, Tsinghua University, 100084, Beijing, China.

DS-Cav1, SC-TM, and DS2 are distinct designer pre-fusion F proteins (pre-F) of respiratory syncytial virus (RSV) developed for vaccines. However, their immunogenicity has not been directly compared. In this study, we generated three recombinant vaccines using the chimpanzee adenovirus vector AdC68 to express DS-Cav1, SC-TM, and DS2.

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Article Synopsis
  • Respiratory syncytial virus (RSV) commonly causes severe respiratory infections, especially in infants and vulnerable populations, and predicting its clinical course can be challenging as many severe cases occur in healthy individuals.
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Article Synopsis
  • Disease outbreaks pose significant risks to great apes and wildlife, and understanding social networks is crucial for predicting how diseases spread among these populations.
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A mucosal route of vaccination could prevent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) replication at the site of infection and limit transmission. We compared protection against heterologous XBB.1.

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COVID-19 vaccines have successfully reduced severe disease and death after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Nonetheless, COVID-19 vaccines are variably effective in preventing transmission and symptomatic SARS-CoV-2 infection. Here, we evaluated the impact of mucosal or intramuscular vaccine immunization on airborne infection and transmission of SARS-CoV-2 in Syrian hamsters.

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