Pediatric antibody responses to SARS-CoV-2 after infection and vaccination in Calgary, Canada.

Publication date: Jul 18, 2024

There are few reports of longitudinal serologic responses in children following Sars-CoV-2 infection and vaccination. This study describes longitudinal SARS-CoV-2 antibody responses following infection, vaccination, or both (hybrid immunity) in a cohort of Canadian children. The objectives of our study were to compare antibody levels following SARS-CoV-2 infection, vaccination, and hybrid immunity and to examine antibody decline after final antigen exposure. The Alberta Childhood COVID-19 Cohort (AB3C) study was a prospective longitudinal cohort study conducted from July 2020 to September 2022 with repeat sampling across 5 visits. Children under 18 years of age were enrolled for serial measurement of antibody responses to SARS-CoV-2 virus vaccine and infection. The final sample size was 919; participants were 50. 5% female, 48. 2% were > 12 years and 88. 5% were white ethnicity. The median peak spike IgG level of those with only infection was not different from those with no vaccination or infection (233 AU/mL (IQR: 99-944 AU/mL) vs. 3 AU/mL (IQR: 1-5 AU/mL; P = 0. 1765). Participants with infections after vaccination had higher IgG levels than those where infection preceded vaccination (median: 36,660 (IQR: 22,084 - 40,000 AU/mL) vs. 17,461 AU/mL (IQR: 10,617 - 33,212 AU/mL); P 

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Concepts Keywords
Antigen Adolescent
Canada Alberta
July Antibodies, Viral
Vaccination Antibodies, Viral
Antibody Formation
Canada
Child
Child, Preschool
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
Hybrid immunity
Immunoglobulin G
Immunoglobulin G
Infant
Longitudinal Studies
Male
Pediatrics
Prospective Studies
SARS-CoV-2
SARS-CoV-2
SARS-CoV-2 immunity
Vaccination

Semantics

Type Source Name
disease MESH infection
disease VO vaccination
disease VO Canada
disease MESH Sars-CoV-2 infection
pathway REACTOME SARS-CoV-2 Infection
disease VO vaccine
disease MESH Infectious Diseases
disease MESH clinical importance
disease VO organization
disease VO time
disease VO effectiveness
disease MESH asymptomatic infections
disease IDO blood
disease IDO history
disease IDO process
disease VO report
disease VO unvaccinated
disease VO dose
disease VO vaccine dose
disease MESH asthma
pathway KEGG Asthma
drug DRUGBANK Trestolone
drug DRUGBANK Ademetionine
disease MESH reinfections
disease VO population
disease MESH emergency
disease VO age
disease VO vaccinated
disease MESH breakthrough infection
disease IDO immune response
disease MESH celiac disease
disease MESH ADHD
disease MESH cardiovascular disease
disease MESH cancer
disease IDO cell
disease VO frequency
drug DRUGBANK Hyaluronic acid
drug DRUGBANK Etoperidone
disease MESH Nosocomial Infection
disease MESH virus infection
disease IDO assay
drug DRUGBANK BIA

Original Article

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