Immunogenicity and Effectiveness of Primary and Booster Vaccine Combination Strategies during Periods of SARS-CoV-2 Delta and Omicron Variants

dc.contributor.authorMoghnieh, Rima A.
dc.contributor.authorEl Hajj, Claude
dc.contributor.authorAbdallah, Dania Issam
dc.contributor.authorJbeily, Nayla
dc.contributor.authorBizri, Abdul Rahman N.
dc.contributor.authorSayegh, Mohamed H.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:19Z
dc.date.available2025-01-24T11:44:19Z
dc.date.issued2022
dc.description.abstractIn this study involving a cohort of employees of the National Airline company in Lebanon, we assessed humoral immunity levels and the effectiveness of two COVID-19 vaccines, Gam-COVID-Vac versus BNT162b2, after two doses and after a homologous and heterologous BNT162b2 booster, in addition to the impact of hybrid immunity. Vaccine effectiveness (VE) was retrospectively determined against laboratory-confirmed SARS-CoV-2 infection during the periods of Delta and Omicron variants’ predominance, separately, and was calculated based on a case–control study design. The humoral immune response, measured by a SARS-CoV-2 anti-spike receptor-binding domain (RBD) IgG titer, was prospectively assessed after the aforementioned vaccination schemes at different time points. This study showed higher effectiveness of BNT162b2 after two doses (81%) compared to two doses of Gam-COVID-Vac (41.8%) against the Delta variant of SARS-CoV-2, which correlated with anti-spike antibody levels. Regarding the Omicron variant, protection against infection and antibody levels were severely compromised and the correlation between an anti-spike IgG titer and effectiveness was lost, unlike the situation during the Delta wave. Considering the booster vaccination schemes, a homologous BNT162b2 booster after a BNT162b2 primary vaccination induced a higher humoral immune response when compared to that induced by a heterologous BNT162b2 booster after a Gam-COVID-Vac primary vaccination. However, the VE of both booster regimens against the Omicron variant was almost equal (64% in the homologous regimen and 57% in heterologous regimen). Hybrid immunity evidenced a better humoral response and a greater and longer protection against Delta and Omicron infections compared to vaccination-induced immunity in COVID-19-naïve individuals. Finally, the findings show that VE waned with time during the same wave, highlighting the importance of reinforcing primary and booster COVID-19 vaccination mainly at the beginning of each wave during the surge of a new variant of concern. © 2022 by the authors.
dc.identifier.doihttps://doi.org/10.3390/vaccines10101596
dc.identifier.eid2-s2.0-85140881299
dc.identifier.urihttp://hdl.handle.net/10938/30433
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofVaccines
dc.sourceScopus
dc.subjectBnt162b2
dc.subjectDelta variant
dc.subjectEffectiveness
dc.subjectGam-covid-vac
dc.subjectHeterologous vaccination
dc.subjectHomologous vaccination
dc.subjectImmunogenicity
dc.subjectLebanon
dc.subjectOmicron variant
dc.subjectSputnik v vaccine
dc.subjectTozinameran
dc.subjectAbdominal pain
dc.subjectAdult
dc.subjectAged
dc.subjectAntibody blood level
dc.subjectArthralgia
dc.subjectArticle
dc.subjectBlood sampling
dc.subjectCase control study
dc.subjectChemoluminescence
dc.subjectChill
dc.subjectCohort analysis
dc.subjectComparative effectiveness
dc.subjectControlled study
dc.subjectCoronavirus disease 2019
dc.subjectDiarrhea
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectDyspnea
dc.subjectE-mail
dc.subjectFemale
dc.subjectFever
dc.subjectHeadache
dc.subjectHuman
dc.subjectHumoral immunity
dc.subjectImmune response
dc.subjectImmunization
dc.subjectImmunoassay
dc.subjectInjection site pain
dc.subjectLethargy
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectMyalgia
dc.subjectNausea
dc.subjectNonhuman
dc.subjectPandemic
dc.subjectPolymerase chain reaction
dc.subjectProspective study
dc.subjectReceptor binding
dc.subjectRetrospective study
dc.subjectSars-cov-2 delta
dc.subjectSars-cov-2 omicron
dc.subjectVaccination
dc.subjectVariant of concern
dc.subjectVomiting
dc.titleImmunogenicity and Effectiveness of Primary and Booster Vaccine Combination Strategies during Periods of SARS-CoV-2 Delta and Omicron Variants
dc.typeArticle

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