Characterization of Vaccine-Enhanced Humoral Immune Responses Against Emergent SARS-CoV-2 Variants in a Convalescent Cohort.

Publication date: Jan 08, 2025

Vaccination of COVID-19-convalescent individuals may generate ‘hybrid’ immunity of enhanced magnitude, durability, and cross-reactive breadth. Our primary goal was to characterize hybrid antibody (Ab) responses in a patient cohort infected with ancestral Wuhan-Hu-1 virus and vaccinated between 6 and 10 months later with the Wuhan-Hu-1-based BNT162b2 mRNA vaccine. We were particularly interested in determining the efficacy of neutralizing Ab responses against subsequently emergent SARS-CoV-2 variants. Sera collected at 3-monthly intervals over a period of 12 months were analyzed by ELISA for SARS-CoV-2 RBD-specific Ab responses, and also for neutralizing Ab activity using pseudovirus-based neutralization assays. We found that convalescent RBD-reactive IgG and IgA Ab responses did not decline significantly through 9 months post-diagnosis. These responses improved significantly following vaccination and remained elevated through at least 12-months. SARS-CoV-2 neutralizing Ab activity was detected in convalescent sera through 9 months post-diagnosis, although it trended downwards from 3 months. Neutralizing Ab activity against the Wuhan-Hu-1 strain was significantly improved by vaccination, to levels that persisted through the end of the study. However, sera collected from vaccinated convalescent subjects also had significant neutralization activity against Delta B. 1.617. 2 and Omicron variants that persisted for at least 2-3 months, unlike sera from unvaccinated convalescent controls. Thus, vaccination of Wuhan-Hu-1-convalescent individuals with the BNT162b2 vaccine improved and sustained protective neutralizing Ab activity against SARS-CoV-2, including cross-reactive neutralizing activity against variants that emerged months later.

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Concepts Keywords
Bnt162b2 Adult
Improved Aged
Monthly Antibodies, Neutralizing
Pseudovirus Antibodies, Neutralizing
Vaccinated Antibodies, Viral
Antibodies, Viral
BNT162 Vaccine
BNT162 Vaccine
BNT162b2 vaccine
Cohort Studies
Convalescence
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Cross Reactions
Female
Humans
hybrid immunity
Immunity, Humoral
Immunoglobulin A
Immunoglobulin A
Immunoglobulin G
Immunoglobulin G
Male
Middle Aged
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
Vaccination

Semantics

Type Source Name
disease MESH COVID-19
drug DRUGBANK Amber
disease MESH Cancer
drug DRUGBANK Methylergometrine
drug DRUGBANK Spinosad
disease MESH infection
disease IDO blood
drug DRUGBANK Pentaerythritol tetranitrate
disease IDO assay
disease IDO protein
disease IDO production
disease MESH Influenza
drug DRUGBANK Serine
disease IDO host
disease MESH infection transmission
drug DRUGBANK Guanosine
disease MESH reinfections
disease MESH Convalescence

Original Article

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