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Low Neutralizing Activities to the Omicron Subvariants BN.1 and XBB.1.5 of Sera From the Individuals Vaccinated With a BA.4/5-Containing Bivalent mRNA Vaccine.
Nham, Eliel; Kim, Jineui; Lee, Jungmin; Park, Heedo; Kim, Jeonghun; Lee, Sohyun; Choi, Jaeuk; Kim, Kyung Taek; Yoon, Jin Gu; Hwang, Soon Young; Song, Joon Young; Cheong, Hee Jin; Kim, Woo Joo; Park, Man-Seong; Noh, Ji Yun.
Afiliação
  • Nham E; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
  • Kim J; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Lee J; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Park H; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Kim J; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Lee S; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Choi J; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Kim KT; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Yoon JG; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
  • Hwang SY; Department of Biostatistics, Korea University College of Medicine, Seoul 02841, Korea.
  • Song JY; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
  • Cheong HJ; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
  • Kim WJ; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
  • Park MS; Department of Microbiology, Vaccine Innovation Center, Korea University College of Medicine, Seoul 02841, Korea.
  • Noh JY; Division of Infectious Diseases, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Immune Netw ; 23(6): e43, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38188597
ABSTRACT
The continuous emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants has provided insights for updating current coronavirus disease 2019 (COVID-19) vaccines. We examined the neutralizing activity of Abs induced by a BA.4/5-containing bivalent mRNA vaccine against Omicron subvariants BN.1 and XBB.1.5. We recruited 40 individuals who had received a monovalent COVID-19 booster dose after a primary series of COVID-19 vaccinations and will be vaccinated with a BA.4/5-containing bivalent vaccine. Sera were collected before vaccination, one month after, and three months after a bivalent booster. Neutralizing Ab (nAb) titers were measured against ancestral SARS-CoV-2 and Omicron subvariants BA.5, BN.1, and XBB.1.5. BA.4/5-containing bivalent vaccination significantly boosted nAb levels against both ancestral SARS-CoV-2 and Omicron subvariants. Participants with a history of SARS-CoV-2 infection had higher nAb titers against all examined strains than the infection-naïve group. NAb titers against BN.1 and XBB.1.5 were lower than those against the ancestral SARS-CoV-2 and BA.5 strains. These results suggest that COVID-19 vaccinations specifically targeting emerging Omicron subvariants, such as XBB.1.5, may be required to ensure better protection against SARS-CoV-2 infection, especially in high-risk groups.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article