Comparable immune escape capacity between KP.2 and other SARS-CoV-2 variants in the central Chinese population after the first COVID-19 booster.

Publication date: May 22, 2025

The neutralisation ability of homologous and heterologous booster vaccinations against the KP. 2 variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is unknown. Therefore, we aimed to evaluate the neutralisation of the Omicron variants by comparing serum samples from Chinese individuals who received heterologous boosters (from different manufacturers) with those who received homologous boosters (from the same manufacturer) against SARS-CoV-2. We collected serum samples from participants in the homologous (n = 38) and heterologous booster groups (n = 38) over 690 days. Serum pseudo virus neutralisation was tested against the prototype, XBB. 1, JN. 1, and KP. 2 variants to detect neutralisation titres. An enzyme-linked immunosorbent assay was used to measure the total concentration of neutralising antibodies against the receptor binding domain of SARS-CoV-2. Neutralisation assays revealed 12. 3-, 12. 3-, and 11. 4-fold reductions against JN. 1, KP. 2, and XBB. 1 variants, respectively, compared with that against the prototype. However, no significant difference was observed in neutralising antibody titres among the JN. 1, KP. 2, and XBB. 1 Omicron variants. Additionally, homologous boosters and men produced fewer neutralising antibodies compared to heterologous boosters and women. Thus, our results demonstrate that the Omicron variant KP. 2 exhibits similar evasion properties to those observed in other variants.

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Concepts Keywords
Antibodies Adult
Chinese Antibodies, Neutralizing
Coronavirus Antibodies, Neutralizing
Covid Antibodies, Viral
Men Antibodies, Viral
Asian People
Booster vaccine
China
Chinese population
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
East Asian People
Female
Humans
Immune Evasion
Immunization, Secondary
KP.2
Male
Middle Aged
Neutralization Tests
Omicron variant
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
XDV.1

Semantics

Type Source Name
disease MESH COVID-19
disease IDO assay
disease IDO protein
drug DRUGBANK Coenzyme M
disease IDO host
disease MESH infection
disease MESH breakthrough infection

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