Neutralization of omicron subvariants and antigenic cartography following multiple COVID 19 vaccinations and repeated omicron non JN.1 or JN.1 infections.

Publication date: Jan 09, 2025

The ongoing emergence of SARS-CoV-2 variants, combined with antigen exposures from different waves and vaccinations, poses challenges in updating COVID-19 vaccine antigens. We collected 206 sera from individuals with vaccination-only, hybrid immunity, and single or repeated omicron post-vaccination infections (PVIs), including non-JN. 1 and JN. 1, and evaluated neutralization against omicron BA. 5, BA. 2.75, BQ. 1.1, XBB. 1.16, XBB. 1.5, and JN. 1. Neutralizing antibodies exhibited a narrow breadth against BA. 5 and BA. 2.75 and failed to neutralize BQ. 1.1 and XBB lineages after three to five doses of the ancestral monovalent vaccine. Hybrid immunity elicited higher neutralizing titers than vaccination alone, but titers remained relatively low. A single omicron PVI elicited lower neutralization titers to all variants compared to wild-type (WT), indicating immunological imprinting. Repeated omicron PVIs, particularly JN. 1, slightly mitigated these effects by increasing broad neutralization responses to all variants, though not significantly. Antigenic mapping demonstrated that XBB lineages and JN. 1 are antigenically distant from WT and also evaded antibodies induced by earlier omicron variants (BA. 1-5) PVIs. However, repeated JN. 1 PVIs shortened this antigenic distance, indicating broader neutralization across omicron variants. These findings highlight SARS-CoV-2 immunity following various antigen boosts and the impact of repeated omicron JN. 1 exposure on broad immunity, informing future COVID-19 vaccination strategies.

Open Access PDF

Concepts Keywords
Antigenically Adult
Cartography Antibodies, Neutralizing
Covid Antibodies, Neutralizing
Shortened Antibodies, Viral
Vaccinations Antibodies, Viral
Antigenic cartography
Antigens, Viral
Antigens, Viral
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
JN.1
Male
Middle Aged
Neutralization Tests
Omicron
SARS-CoV-2
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
spike protein, SARS-CoV-2
Vaccination
Vaccine

Semantics

Type Source Name
disease MESH COVID 19
disease MESH infections
disease MESH Osteoarthritis
disease MESH Dengue
disease MESH Dengue Hemorrhagic Fever
drug DRUGBANK Coenzyme M
disease MESH reinfection
disease IDO protein
disease IDO infection
disease IDO production
disease MESH influenza
disease IDO history
disease IDO blood
disease MESH point mutations
drug DRUGBANK Proline
disease IDO cell
drug DRUGBANK Cefaclor
drug DRUGBANK Dextrose unspecified form
drug DRUGBANK Carboxymethylcellulose
drug DRUGBANK Immune Globulin Human
disease MESH Emergency
disease IDO host
drug DRUGBANK Etoperidone
pathway REACTOME Reproduction

Original Article

(Visited 1 times, 1 visits today)