The presence of neutralizing antibodies against omicron subvariants among a vaccinated cohort at one year after the first dose of vaccination in Malaysia.

Publication date: Jun 01, 2025

This study assesses the neutralizing antibodies response to Omicron subvariants and examines factors associated with seropositivity in a vaccinated Malaysian cohort. It is a prospective cohort study, conducted between June 2021 and October 2022. Descriptive and binary logistic regression analyses were performed on 1,117 adults aged 18 and above. Among the subvariants, seropositivity rates were: BA. 2 (81. 9%), BA. 1 (68. 4%), and BA. 4/5 (64. 2%). Non-Malaysians had significantly higher odds of testing positive for BA. 2 compared to Malaysians (OR: 8. 009; 95% CI: 1. 273-50. 402). Recipients of AstraZeneca (OR: 3. 955; 95% CI: 2. 414-6. 482) and CanSino (OR: 1. 980; 95% CI: 1. 047-3. 743) vaccines had higher odds of BA. 2 seropositivity compared to Pfizer recipients. For BA. 4/5, individuals aged 60 and above had greater odds of seropositivity (OR: 1. 751; 95% CI: 1. 029-2. 979) compared to those aged 18-39. Chinese ethnicity was associated with lower odds of seropositivity than Malay ethnicity across BA. 1 (OR: 0. 508; 95% CI: 0. 350-0. 736), BA. 2 (OR: 0. 570; 95% CI: 0. 377-0. 861), and BA. 4/5 (OR: 0. 671; 95% CI: 0. 467-0. 963). This study highlights that completing primary vaccination and booster doses remains critical to reducing severe COVID-19 outcomes, underscoring the need for ongoing surveillance and targeted strategies for vulnerable demographic and socio-environmental groups.

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Concepts Keywords
June Adolescent
Malaysians Adult
Vaccines Aged
Antibodies, Neutralizing
Antibodies, Neutralizing
Antibodies, Viral
Antibodies, Viral
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
Malaysia
Malaysia
Male
Middle Aged
Neutralizing antibodies
Omicron variants
Prospective Studies
SARS-CoV-2
Vaccinated cohort
Vaccination
Young Adult

Semantics

Type Source Name
disease MESH COVID-19
disease MESH emergencies
disease IDO protein
disease MESH Infection
disease IDO host
drug DRUGBANK Coenzyme M
pathway REACTOME Immune System
disease IDO adaptive immune response
disease MESH breakthrough infections
disease IDO intervention
disease IDO blood
disease IDO history
disease MESH diabetes mellitus
disease MESH hypertension
disease MESH asthma
pathway KEGG Asthma
disease MESH pulmonary disease
disease MESH cancer
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH systemic lupus erythematosus
pathway KEGG Systemic lupus erythematosus
disease MESH syndrome
disease MESH kidney failure
disease IDO assay
disease IDO process
disease IDO reagent
disease MESH infectious diseases
drug DRUGBANK Aspartame
disease MESH comorbidity

Original Article

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