Equal Maintenance of Anti-SARS-CoV-2 Antibody Levels Induced by Heterologous and Homologous Regimens of the BNT162b2, ChAdOx1, CoronaVac and Ad26.COV2.S Vaccines: A Longitudinal Study Up to the 4th Dose of Booster.

Publication date: Jul 18, 2024

Several technological approaches have been used to develop vaccines against COVID-19, including those based on inactivated viruses, viral vectors, and mRNA. This study aimed to monitor the maintenance of anti-SARS-CoV-2 antibodies in individuals from Brazil according to the primary vaccination regimen, as follows: BNT162b2 (group 1; 22) and ChAdOx1 (group 2; 18). Everyone received BNT162b2 in the first booster while in the second booster CoronaVac, Ad26. COV2. S, or BNT162b2. Blood samples were collected from 2021 to 2023 to analyze specific RBD (ELISA) and neutralizing antibodies (PRNT50). We observed a progressive increase in anti-RBD and neutralizing antibodies in each subsequent dose, remaining at high titers until the end of follow-up. Group 1 had higher anti-RBD antibody titers than group 2 after beginning the primary regimen, with significant differences after the 2nd and 3rd doses. Group 2 showed a more expressive increase after the first booster with BNT162B2 (heterologous booster). Group 2 also presented high levels of neutralizing antibodies against the Gamma and Delta variants until five months after the second booster. In conclusion, the circulating levels of anti-RBD and neutralizing antibodies against the two variants of SARS-CoV-2 were durable even five months after the 4th dose, suggesting that periodic booster vaccinations (homologous or heterologous) induced long-lasting immunity.

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Concepts Keywords
Antibodies anti-RBD antibodies
Brazil BNT162b2
Covid ChAdOx1-S
Inactivated CoronaVac
Months COVID-19
dose booster
neutralizing antibodies
study longitudinal
vaccine effectiveness

Semantics

Type Source Name
drug DRUGBANK Aspartame
disease VO CoronaVac
disease VO Ad26.COV2.S
disease VO dose
disease MESH COVID-19
disease VO Viruses
disease VO primary vaccination
disease IDO blood
disease MESH Malaria
pathway KEGG Malaria
disease VO vaccine effectiveness
disease MESH viral infection
drug DRUGBANK Coenzyme M
disease MESH respiratory failure
disease MESH death
drug DRUGBANK Methylergometrine
drug DRUGBANK Angiotensin II
disease MESH infection
disease VO effectiveness
disease IDO replication
disease VO effective
disease VO efficiency
disease IDO pathogen
disease VO immunization
disease VO Comirnaty
disease VO COVAXIN
disease VO vaccinated
disease VO vaccine
disease VO time
disease VO population
disease IDO production
disease VO vaccination
disease VO secondary vaccination
disease VO USA
drug DRUGBANK Water
disease MESH Psoriasis
disease MESH Hypertension
disease MESH Obesity
drug DRUGBANK Indoleacetic acid
drug DRUGBANK Saquinavir
drug DRUGBANK Cefaclor
drug DRUGBANK Carboxymethylcellulose
drug DRUGBANK Formaldehyde
drug DRUGBANK Gentian violet cation
disease VO immunized
disease VO ANOVA
disease MESH seroconversion
disease VO titer
disease IDO history
disease IDO process
disease VO protocol
drug DRUGBANK Efavirenz
disease IDO assay
drug DRUGBANK Fluticasone furoate
drug DRUGBANK Sennosides
drug DRUGBANK (S)-Des-Me-Ampa
disease VO vaccine dose
drug DRUGBANK Ribostamycin
drug DRUGBANK Cyclic Adenosine Monophosphate

Original Article

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