Neutralizing antibody evasion of SARS-CoV-2 JN.1 derivatives KP.3, KP.3.1.1, LB.1, and XEC.

Publication date: Jul 09, 2025

The emergence of SARS-CoV-2 variants poses ongoing challenges to vaccine efficacy. We evaluated neutralizing antibody responses against JN. 1 and its derivatives (KP. 3, KP. 3.1. 1, LB. 1, and XEC) in healthcare workers who received seven doses of BNT162b2, including the XBB. 1.5 monovalent vaccine. In COVID-19-nacEFve individuals, KP. 3.1. 1 and LB. 1 showed substantial immune escape, whereas previously infected individuals maintained neutralization activity against all variants. We also demonstrated that JN. 1-based immunization induces robust cross-neutralizing activity against emerging variants. A single amino acid deletion at position 31 in the spike protein may be associated with enhanced immune evasion. These findings support the potential effectiveness of JN. 1-based vaccines while highlighting the need for continued surveillance and vaccine optimization.

Concepts Keywords
Bnt162b2 COVID-19
Covid Immune escape
Efficacy JN.1
Vaccines KP.3.1.1
Workers Omicron
XEC

Semantics

Type Source Name
disease MESH COVID-19
disease IDO protein

Original Article

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