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Evolving antibody response to SARS-CoV-2 antigenic shift from XBB to JN.1
Fanchong Jian1,2,3, Jing Wang1,2,4, Ayijiang Yisimayi1,2,4
1Biomedical Pioneering Innovation Center (BIOPIC), Peking University, Beijing, China.
The JN.1 SARS-CoV-2 variant shows distinct immune responses compared to XBB, with JN.1 infection providing better neutralization against its own subvariants. Booster updates are needed due to immune evasion by variants like KP.3.
Area of Science:
- Immunology
- Virology
- Vaccinology
Background:
- SARS-CoV-2 continuously evolves, with the JN.1 lineage succeeding XBB.
- Understanding the immune response to new variants is crucial for vaccine development.
Purpose of the Study:
- To analyze the humoral immune response to XBB and JN.1 exposure.
- To assess the effectiveness of antibodies against emerging SARS-CoV-2 variants.
Main Methods:
- Analysis of plasma neutralization against XBB and JN.1.
- Deep mutational scanning of antibody epitopes.
- Characterization of B cell receptor repertoire.
Main Results:
- JN.1 infection elicits superior neutralization against its subvariants compared to XBB.
- KP.3 exhibits significant immune evasion and receptor-binding capability.
- JN.1-induced memory B cells are superior; however, KP.2 and KP.3 evade some JN.1-induced antibodies.
Conclusions:
- The antigenic shift from XBB to JN.1 necessitates vaccine composition re-evaluation.
- JN.1 lineage, particularly KP.2 and KP.3, should be considered for vaccine boosters.
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