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Neutralization of SARS-CoV-2 lineage B.1.1.7 pseudovirus by BNT162b2 vaccine-elicited human sera
Alexander Muik; Ann-Kathrin Wallisch; Bianca Saenger; Kena A Swanson; Julia Muehl; Wei Chen; Hui Cai; Ritu Sarkar; Oezlem Tuereci; Philip R Dormitzer; Ugur Sahin.
Affiliation
  • Alexander Muik; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
  • Ann-Kathrin Wallisch; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
  • Bianca Saenger; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
  • Kena A Swanson; Pfizer, 401 N Middletown Rd., Pearl River, NY 10965 USA
  • Julia Muehl; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
  • Wei Chen; Pfizer, 401 N Middletown Rd., Pearl River, NY 10965 USA
  • Hui Cai; Pfizer, 401 N Middletown Rd., Pearl River, NY 10965 USA
  • Ritu Sarkar; Pfizer, 401 N Middletown Rd., Pearl River, NY 10965 USA
  • Oezlem Tuereci; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
  • Philip R Dormitzer; Pfizer, 401 N Middletown Rd., Pearl River, NY 10965 USA
  • Ugur Sahin; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany
Preprint in English | bioRxiv | ID: ppbiorxiv-426984
ABSTRACT
Recently, a new SARS-CoV-2 lineage called B.1.1.7 has emerged in the United Kingdom that was reported to spread more efficiently than other strains. This variant has an unusually large number of mutations with 10 amino acid changes in the spike protein, raising concerns that its recognition by neutralizing antibodies may be affected. Here, we investigated SARS-CoV-2-S pseudoviruses bearing either the Wuhan reference strain or the B.1.1.7 lineage spike protein with sera of 16 participants in a previously reported trial with the mRNA-based COVID-19 vaccine BNT162b2. The immune sera had equivalent neutralizing titers to both variants. These data, together with the combined immunity involving humoral and cellular effectors induced by this vaccine, make it unlikely that the B.1.1.7 lineage will escape BNT162b2-mediated protection.
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Rct Language: English Year: 2021 Document type: Preprint
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