Neutralization of SARS-CoV-2 Omicron subvariant BA.2.87.1
- PMID: 38458874
- PMCID: PMC12117944
- DOI: 10.1016/j.vaccine.2024.03.007
Neutralization of SARS-CoV-2 Omicron subvariant BA.2.87.1
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.
Keywords: BA.2.87.1; Neutralizing antibody; Omicron; SARS-CoV-2; mRNA.
Copyright © 2024. Published by Elsevier Ltd.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Figures
References
-
- Stankov MV, Hoffmann M, Gutierrez Jauregui R, et al. Humoral and cellular immune responses following BNT162b2 XBB.1.5 vaccination. Lancet Infect Dis 2024;24:e1–3. - PubMed
-
- Marking U, Bladh O, Aguilera K, et al. Humoral immune responses to the monovalent XBB.1.5-adapted BNT162b2 mRNA booster in Sweden. The Lancet Infectious Diseases. - PubMed
-
- Link-Gelles R CA, Mak J, et al. Early estimates of updated 2023–2024 (Monovalent XBB.1.5) COVID-19 Vaccine effectiveness against symptomatic SARS-CoV-2 infection attributable to co-circulating omicron variants among immunocompetent adults — increasing community access to testing program, United States, September 2023–January 2024. MMWR Morb Mortal Wkly Rep 2024;73:77–83. - PMC - PubMed
Publication types
MeSH terms
Substances
Supplementary concepts
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
