Evaluation of population immunity against SARS-CoV-2 variants, EG.5.1, FY.4, BA.2.86, JN.1, JN.1.4, and KP.3.1.1 using samples from two health demographic surveillance systems in Kenya.

Publication date: Dec 28, 2024

Increased immune evasion by emerging and highly mutated SARS-CoV-2 variants is a key challenge to the control of COVID-19. The majority of these mutations mainly target the spike protein, allowing the new variants to escape the immunity previously raised by vaccination and/or infection by earlier variants of SARS-CoV-2. In this study, we investigated the neutralizing capacity of antibodies against emerging variants of interest circulating between May 2023 and October 2024 using sera from representative samples of the Kenyan population. From our genomics data, we identified the most prevalent Kenyan and global variants and performed pseudoviruses neutralization assays with the most recent SARS-CoV-2 variants. Our data show that antibodies from individuals in the general population in Kenya were less effective against the recent prevalent SARS-CoV-2 omicron variants (i. e. EG. 5.1, FY. 4, BA. 2.86, JN. 1, JN. 1.4, and KP. 3.1. 1) compared to the ancestral wildtype strain. Although there was increased neutralization following multiple doses of vaccine, antibodies from > 40% of the vaccinated individuals did not neutralize the omicron variants, suggesting that individuals were susceptible to infection by these variants.

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Concepts Keywords
Kenya Adolescent
October Adult
Protein Aged
Pseudoviruses Antibodies, Neutralizing
Vaccination Antibodies, Neutralizing
Antibodies, Viral
Antibodies, Viral
COVID-19
Female
Humans
Kenya
Male
Middle Aged
Mutation
Neutralization
Population immunity
SARS-CoV-2
SARS-CoV-2 variants
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
Vaccination
Young Adult

Semantics

Type Source Name
disease IDO production
disease IDO host
disease MESH infection transmission
disease MESH Infectious Diseases
pathway REACTOME Reproduction
disease MESH infection
disease IDO protein
disease MESH COVID-19
drug DRUGBANK Hyaluronic acid
disease IDO infectivity
drug DRUGBANK Serine
disease MESH tic
disease IDO country
pathway REACTOME Immune System
drug DRUGBANK Ademetionine
disease MESH Avian Influenza
disease IDO site
drug DRUGBANK Coenzyme M
disease IDO assay
disease IDO cell
drug DRUGBANK Indoleacetic acid
disease IDO blood
disease MESH reinfection
drug DRUGBANK Fosfomycin
pathway REACTOME Signal Transduction
disease MESH Influenza

Original Article

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