| Literature DB >> 35579540 |
Peter J Halfmann1, Makoto Kuroda1, Tammy Armbrust1, James Theiler2, Ariane Balaram1, Gage K Moreno3, Molly A Accola4, Kiyoko Iwatsuki-Horimoto5, Riccardo Valdez6, Emily Stoneman7, Katarina Braun1, Seiya Yamayoshi5, Elizabeth Somsen3, John J Baczenas3,8, Keiko Mitamura9, Masao Hagihara10, Eisuke Adachi11, Michiko Koga12, Matthew McLaughlin3, William Rehrauer3,4, Masaki Imai5, Shinya Yamamoto12, Takeya Tsutsumi12, Makoto Saito12, Thomas C Friedrich1,8, Shelby L O'Connor3,8, David H O'Connor3,8, Aubree Gordon13, Bette Korber14,15, Yoshihiro Kawaoka1,5,16.
Abstract
The SARS-CoV-2 B.1.621 (Mu) variant emerged in January 2021 and was categorized as a variant of interest by the World Health Organization in August 2021. This designation prompted us to study the sensitivity of this variant to antibody neutralization. In a live virus neutralization assay with serum samples from individuals vaccinated with the Pfizer/BioNTech or Moderna mRNA vaccines, we measured neutralization antibody titers against B.1.621, an early isolate (spike 614D), and a variant of concern (B.1.351, Beta variant). We observed reduced neutralizing antibody titers against the B.1.621 variant (3.4- to 7-fold reduction, depending on the serum sample and time after the second vaccination) compared to the early isolate and a similar reduction when compared to B.1.351. Likewise, convalescent serum from hamsters previously infected with an early isolate neutralized B.1.621 to a lower degree. Despite this antibody titer reduction, hamsters could not be efficiently rechallenged with the B.1.621 variant, suggesting that the immune response to the first infection is adequate to provide protection against a subsequent infection with the B.1.621 variant.Entities:
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Year: 2022 PMID: 35579540 PMCID: PMC9392899 DOI: 10.1126/scitranslmed.abm4908
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 19.319