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BNT162b2 Versus mRNA-1273 Vaccines: Comparative Analysis of Long-Term Protection Against SARS-CoV-2 Infection and Severe COVID-19 in Qatar.
Chemaitelly, Hiam; Ayoub, Houssein H; Coyle, Peter; Tang, Patrick; Hasan, Mohammad R; Yassine, Hadi M; Al Thani, Asmaa A; Al-Kanaani, Zaina; Al-Kuwari, Einas; Jeremijenko, Andrew; Kaleeckal, Anvar Hassan; Latif, Ali Nizar; Shaik, Riyazuddin Mohammad; Abdul-Rahim, Hanan F; Nasrallah, Gheyath K; Al-Kuwari, Mohamed Ghaith; Butt, Adeel A; Al-Romaihi, Hamad Eid; Al-Thani, Mohamed H; Al-Khal, Abdullatif; Bertollini, Roberto; Abu-Raddad, Laith J.
Afiliação
  • Chemaitelly H; Infectious Disease Epidemiology Group, Weill Cornell Medicine-Qatar, Cornell University, Doha, Qatar.
  • Ayoub HH; World Health Organization Collaborating Centre for Disease Epidemiology Analytics on HIV/AIDS, Sexually Transmitted Infections, and Viral Hepatitis, Weill Cornell Medicine-Qatar, Cornell University, Qatar Foundation - Education City, Doha, Qatar.
  • Coyle P; Department of Population Health Sciences, Weill Cornell Medicine, Cornell University, New York, New York, USA.
  • Tang P; Mathematics Program, Department of Mathematics and Statistics, College of Arts and Sciences, Qatar University, Doha, Qatar.
  • Hasan MR; Department of Biomedical Science, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Yassine HM; Hamad Medical Corporation, Doha, Qatar.
  • Al Thani AA; Wellcome-Wolfson Institute for Experimental Medicine, Queens University, Belfast, UK.
  • Al-Kanaani Z; Department of Pathology, Sidra Medicine, Doha, Qatar.
  • Al-Kuwari E; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
  • Jeremijenko A; Department of Biomedical Science, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Kaleeckal AH; Biomedical Research Center, QU Health, Qatar University, Doha, Qatar.
  • Latif AN; Department of Biomedical Science, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Shaik RM; Biomedical Research Center, QU Health, Qatar University, Doha, Qatar.
  • Abdul-Rahim HF; Hamad Medical Corporation, Doha, Qatar.
  • Nasrallah GK; Hamad Medical Corporation, Doha, Qatar.
  • Al-Kuwari MG; Hamad Medical Corporation, Doha, Qatar.
  • Butt AA; Hamad Medical Corporation, Doha, Qatar.
  • Al-Romaihi HE; Hamad Medical Corporation, Doha, Qatar.
  • Al-Thani MH; Hamad Medical Corporation, Doha, Qatar.
  • Al-Khal A; Department of Public Health, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Bertollini R; Department of Biomedical Science, College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Abu-Raddad LJ; Biomedical Research Center, QU Health, Qatar University, Doha, Qatar.
Influenza Other Respir Viruses ; 18(10): e13357, 2024 Oct.
Article em En | MEDLINE | ID: mdl-39343986
ABSTRACT

BACKGROUND:

This study provides a head-to-head comparison of the protection provided by the BNT162b2 and mRNA-1273 vaccines against SARS-CoV-2 infection and against severe COVID-19, covering primary series and third dose/booster vaccinations over up to 3 years of follow-up, both before and after the emergence of the omicron variant.

METHODS:

Two national, matched, retrospective cohort studies were conducted on Qatar's vaccinated population from December 16, 2020, to February 18, 2024. Subgroup analyses by pre-vaccination SARS-CoV-2 infection history, as well as sensitivity analyses, were also conducted.

RESULTS:

The adjusted hazard ratio (AHR) comparing infection incidence in those vaccinated with BNT162b2 versus mRNA-1273 was 1.03 (95% CI 1.02-1.05) after the primary series and 1.11 (95% CI 1.09-1.13) after the third (booster) dose. The corresponding AHRs for any severe, critical, or fatal COVID-19 were 1.31 (95% CI 0.81-2.11) and 1.00 (95% CI 0.20-4.94), respectively. Subgroup analyses by prior infection status hinted at a dose-dependent immune imprinting effect, where a combination of two types of immunity, pre-omicron and omicron, offered greater protection against infection than one type alone, with this effect being amplified by the higher antigen dose of mRNA-1273 compared to BNT162b2. Sensitivity analyses confirmed the study findings.

CONCLUSIONS:

BNT162b2 provided slightly less protection against infection than mRNA-1273 following both primary series and booster vaccinations while offering comparable protection against severe COVID-19 outcomes. The findings suggested that the vaccine antigen dose in interaction with infection history may determine the extent of immune protection against infection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra COVID-19 / SARS-CoV-2 / COVID-19 / Vacina BNT162 / Vacina de mRNA-1273 contra 2019-nCoV Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Influenza Other Respir Viruses Assunto da revista: VIROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Qatar País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra COVID-19 / SARS-CoV-2 / COVID-19 / Vacina BNT162 / Vacina de mRNA-1273 contra 2019-nCoV Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Influenza Other Respir Viruses Assunto da revista: VIROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Qatar País de publicação: Reino Unido