Persistent differences in the immunogenicity of the two COVID-19 primary vaccines series, modulated by booster mRNA vaccination and breakthrough infection.

Persistent differences in the immunogenicity of the two COVID-19 primary vaccines series, modulated by booster mRNA vaccination and breakthrough infection.

Publication date: May 09, 2024

The long-term impact of initial immunogenicity induced by different primary COVID-19 vaccine series remains unclear. A prospective cohort study was conducted at 10 tertiary hospitals in Korea from March 2021 to September 2022. Immunogenicity assessments included anti-spike protein antibody (Sab), SARS-CoV-2-specific interferon-gamma releasing assay (IGRA), and multiplex cytokine assays for spike protein-stimulated plasma. Spike proteins derived from wild-type SARS-CoV-2 and alpha variant (Spike) and beta and gamma variant (Spike) were utilized. A total of 235 healthcare workers who had received a two-dose primary vaccine series of either ChAdOx1 or BNT162b2, followed by a third booster dose of BNT162b2 (166 in the ChAdOx1/ChAdOx1/BNT162b2 (CCB) group and 69 in the BNT162b2/BNT162b2/BNT162b2 (BBB) group, based on the vaccine series) were included. Following the primary vaccine series, the BBB group exhibited significantly higher increases in Sab levels, IGRA responses, and multiple cytokines (CCL2/MCP-1, CCL3/MIP-1α, CCL4/MIP-1β, interleukin (IL)-1ra, IFN-γ, IL-2, IL-4, and IL-10) compared to the CCB group (all P

Concepts Keywords
Bnt162b2 Breakthrough infection
Korea COVID-19
September Cytokine
Vaccines Interferon-gamma releasing assay
Workers SARS-CoV-2
Vaccine

Semantics

Type Source Name
disease MESH COVID-19
disease VO vaccination
disease MESH breakthrough infection
disease VO COVID-19 vaccine
drug DRUGBANK Dihydrotachysterol
disease IDO assay
disease VO dose
disease VO vaccine
drug DRUGBANK Binetrakin
drug DRUGBANK Interleukin-10
disease MESH Breakthrough infection COVID-19

Original Article

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