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bioRxiv · 10.1101/2024.11.04.621772

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

Sano, K.·Miyakawa, K.·Kato, H.·Kimura, Y.·Goto, A.·Ryo, A.·Watanabe, S.·Hasegawa, H.
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Abstract

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 XBB.1.5 monovalent vaccine. In COVID-19-naive individuals, KP.3.1.1 and LB.1 showed substantial immune escape, while 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 significantly impacted immune evasion. These findings support the potential effectiveness of JN.1-based vaccines while highlighting the need for continued surveillance and vaccine optimization.

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Sano, K., Miyakawa, K., Kato, H., Kimura, Y., Goto, A., Ryo, A., Watanabe, S., Hasegawa, H.. 2024-11-05. Neutralizing antibody evasion of SARS-CoV-2 JN.1 derivatives KP.3, KP.3.1.1, LB.1, and XEC. https://doi.org/10.1101/2024.11.04.621772

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