Immunogenicity and Effectiveness of Primary and Booster Vaccine Combination Strategies during Periods of SARS-CoV-2 Delta and Omicron Variants
| dc.contributor.author | Moghnieh, Rima A. | |
| dc.contributor.author | El Hajj, Claude | |
| dc.contributor.author | Abdallah, Dania Issam | |
| dc.contributor.author | Jbeily, Nayla | |
| dc.contributor.author | Bizri, Abdul Rahman N. | |
| dc.contributor.author | Sayegh, Mohamed H. | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:44:19Z | |
| dc.date.available | 2025-01-24T11:44:19Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | In 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.doi | https://doi.org/10.3390/vaccines10101596 | |
| dc.identifier.eid | 2-s2.0-85140881299 | |
| dc.identifier.uri | http://hdl.handle.net/10938/30433 | |
| dc.language.iso | en | |
| dc.publisher | MDPI | |
| dc.relation.ispartof | Vaccines | |
| dc.source | Scopus | |
| dc.subject | Bnt162b2 | |
| dc.subject | Delta variant | |
| dc.subject | Effectiveness | |
| dc.subject | Gam-covid-vac | |
| dc.subject | Heterologous vaccination | |
| dc.subject | Homologous vaccination | |
| dc.subject | Immunogenicity | |
| dc.subject | Lebanon | |
| dc.subject | Omicron variant | |
| dc.subject | Sputnik v vaccine | |
| dc.subject | Tozinameran | |
| dc.subject | Abdominal pain | |
| dc.subject | Adult | |
| dc.subject | Aged | |
| dc.subject | Antibody blood level | |
| dc.subject | Arthralgia | |
| dc.subject | Article | |
| dc.subject | Blood sampling | |
| dc.subject | Case control study | |
| dc.subject | Chemoluminescence | |
| dc.subject | Chill | |
| dc.subject | Cohort analysis | |
| dc.subject | Comparative effectiveness | |
| dc.subject | Controlled study | |
| dc.subject | Coronavirus disease 2019 | |
| dc.subject | Diarrhea | |
| dc.subject | Drug efficacy | |
| dc.subject | Drug safety | |
| dc.subject | Dyspnea | |
| dc.subject | ||
| dc.subject | Female | |
| dc.subject | Fever | |
| dc.subject | Headache | |
| dc.subject | Human | |
| dc.subject | Humoral immunity | |
| dc.subject | Immune response | |
| dc.subject | Immunization | |
| dc.subject | Immunoassay | |
| dc.subject | Injection site pain | |
| dc.subject | Lethargy | |
| dc.subject | Major clinical study | |
| dc.subject | Male | |
| dc.subject | Myalgia | |
| dc.subject | Nausea | |
| dc.subject | Nonhuman | |
| dc.subject | Pandemic | |
| dc.subject | Polymerase chain reaction | |
| dc.subject | Prospective study | |
| dc.subject | Receptor binding | |
| dc.subject | Retrospective study | |
| dc.subject | Sars-cov-2 delta | |
| dc.subject | Sars-cov-2 omicron | |
| dc.subject | Vaccination | |
| dc.subject | Variant of concern | |
| dc.subject | Vomiting | |
| dc.title | Immunogenicity and Effectiveness of Primary and Booster Vaccine Combination Strategies during Periods of SARS-CoV-2 Delta and Omicron Variants | |
| dc.type | Article |
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