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Safety, immunogenicity, and protection provided by unadjuvanted and adjuvanted formulations of a recombinant plant-derived virus-like particle vaccine candidate for COVID-19 in nonhuman primates.
Cell Mol Immunol
34
2022
CD4, CD4 T cells, COVID-19, CoVLP, IL-2, IL-4, SARS, SARS-CoV, SARS-CoV-2, SARS-CoV-2 spike protein, SARS-CoV-2-infected cells, coronavirus disease, cytidine, cytidine-phospho-guanosine, immune cell infiltrates, influenza, interleukin-2, plaque, rhesus macaques, severe acute respiratory syndrome coronavirus 2
Author NameAffiliation
Prabhu S ArunachalamInstitute for Immunity, Stanford University School of Medicine, Stanford University
Nadia A GoldenTulane National Primate Research Center
Jane FontenotNew Iberia Research Center, University of Louisiana at Lafayette
Pyone P AyeTulane National Primate Research Center
Katharina RöltgenStanford University School of Medicine, Stanford University
Kasi E Russell-LodrigueTulane National Primate Research Center
Christopher MonjureTulane National Primate Research Center
Scott D BoydStanford University School of Medicine, Stanford University
Rudolf P BohmTulane National Primate Research Center
Jay RappaportTulane National Primate Research Center
Jay RappaportTulane University School of Medicine
Francois VillingerNew Iberia Research Center, University of Louisiana at Lafayette
Bali PulendranInstitute for Immunity, Stanford University School of Medicine, Stanford University
Bali PulendranStanford University School of Medicine, Stanford University
Bali PulendranStanford University School of Medicine, Stanford University
Bali PulendranInstitute for Immunity, Stanford University School of Medicine, Stanford University
Bali PulendranInstitute for Immunity, Stanford University School of Medicine, Stanford University
Bali PulendranStanford University School of Medicine, Stanford University
Bali PulendranStanford University School of Medicine, Stanford University
Bali PulendranInstitute for Immunity, Stanford University School of Medicine, Stanford University
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