
Articles
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Dec 6, 2024 |
cell.com | Kaitlin R Sprouse |Marcos Miranda |Nicholas J. Catanzaro |Amin Addetia |Cameron Stewart |Jack Brown | +19 more
KeywordsMERS-CoVEMPEMnanoparticlevaccineRBDNTDspikeResearch topic(s)CP: ImmunologyIntroductionThe recent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the human and economic toll that can accompany the spillover and spread of a zoonotic disease in humans. Although the success of vaccine development efforts in response to the pandemic were a triumph of modern vaccinology, SARS-CoV-2 remains the only coronavirus for which licensed vaccines are available.
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Nov 13, 2024 |
science.org | Sharon Saydah |Michael J Peluso |Julio César Silva |Júlio Silva |Alexandra Schafer
AbstractThe severe acute respiratory syndrome coronavirus 2 (SARS-CoV 2) pandemic has caused more than 7 million deaths globally. Despite the presence of infection- and vaccine-induced immunity, SARS-CoV-2 infections remain a major global health concern because of the emergence of SARS-CoV-2 variants that can cause severe acute coronavirus disease 2019 (COVID-19) or enhance Long Covid disease phenotypes.
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Jun 27, 2024 |
nature.com | Cameron Stewart |Alexandra Schafer |Young-Jun Park |John Powers |Davide Corti |Ralph S Baric | +1 more
AbstractEvolution of SARS-CoV-2 alters the antigenicity of the immunodominant spike (S) receptor-binding domain and N-terminal domain, undermining the efficacy of vaccines and antibody therapies. To overcome this challenge, we set out to develop a vaccine focusing antibody responses on the highly conserved but metastable S2 subunit, which folds as a spring-loaded fusion machinery.
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May 3, 2024 |
nature.com | Elizabeth Anderson |Jennifer Diaz |Sarah R. Leist |Alexandra Schafer |John Powers |Ralph S Baric | +2 more
AbstractWhole virus-based inactivated SARS-CoV-2 vaccines adjuvanted with aluminum hydroxide have been critical to the COVID-19 pandemic response.
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Apr 21, 2024 |
cell.com | Alexandra Schafer |Andrea Marzi |Wakako Furuyama |Nicholas J. Catanzaro
Highlights•CC genetic reference population identifies genetic loci regulating EBOV pathogenesis in mice•An F2 population from two CC lines is either highly resistant or vulnerable to EBOV infection•A major locus on chromosome 7, encoding Trim5, drives severe EVD-like disease in mice•Gene expression signatures of liver damage mirror severe EVD in humansSummaryEbola virus (EBOV), a major global health concern, causes severe, often fatal EBOV disease (EVD) in humans.
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