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Neutralization of SARS-CoV-2 Omicron subvariant BA.2.87.1.
Lasrado, Ninaad; Rössler, Annika; Rowe, Marjorie; Collier, Ai-Ris Y; Barouch, Dan H.
Afiliación
  • Lasrado N; Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
  • Rössler A; Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
  • Rowe M; Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
  • Collier AY; Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
  • Barouch DH; Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. Electronic address: dbarouch@bidmc.harvard.edu.
Vaccine ; 42(9): 2117-2121, 2024 Apr 02.
Article en En | MEDLINE | ID: mdl-38458874
ABSTRACT
A new highly mutated Omicron subvariant BA.2.87.1 has recently been identified with over 30 amino acid mutations in the Spike protein compared with BA.2, BA.5, XBB.1.5, and JN.1 variants. Mutiple mutations in BA.2.87.1 are located in the N-terminal domain (NTD) rather than in the receptor binding domain (RBD) of the Spike protein. We evaluated neutralizing antibody (NAb) responses to BA.2.87.1 because of its highly mutated sequence and its unique NTD region. Our data show that NAb responses to BA.2.87.1 were lower than to BA.2 but higher than to JN.1, suggesting that BA.2.87.1 is not a further antibody escape variant compared with other currently circulating variants. Moreover, XBB.1.5 mRNA boosting increased NAb titers to all variants tested including BA.2.87.1.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Límite: Humans Idioma: En Revista: Vaccine Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: COVID-19 Límite: Humans Idioma: En Revista: Vaccine Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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