Author: Kena A. Swanson

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Preprints

Improved Neutralization of Omicron BA.4/5, BA.4.6, BA.2.75.2, BQ.1.1, and XBB.1 with Bivalent BA.4/5 Vaccine

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Six Month Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine

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A prefusion SARS-CoV-2 spike RNA vaccine is highly immunogenic and prevents lung infection in non-human primates

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RNA-Based COVID-19 Vaccine BNT162b2 Selected for a Pivotal Efficacy Study

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Phase 1/2 Study to Describe the Safety and Immunogenicity of a COVID-19 RNA Vaccine Candidate (BNT162b1) in Adults 18 to 55 Years of Age: Interim Report

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Neutralization of N501Y mutant SARS-CoV-2 by BNT162b2 vaccine-elicited sera

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Neutralization of spike 69/70 deletion, E484K, and N501Y SARS-CoV-2 by BNT162b2 vaccine-elicited sera

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Neutralization of SARS-CoV-2 lineage B.1.1.7 pseudovirus by BNT162b2 vaccine-elicited human sera

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Concurrent human antibody andTH1 type T-cell responses elicited by a COVID-19 RNA vaccine

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Neutralization of Omicron SARS-CoV-2 by 2 or 3 doses of BNT162b2 vaccine

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BNT162b vaccines are immunogenic and protect non-human primates against SARS-CoV-2

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Exposure to BA.4/BA.5 Spike glycoprotein drives pan-Omicron neutralization in vaccine-experienced humans and mice

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BNT162b2-Elicited Neutralization of Delta Plus, Lambda, and Other Variants

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