Early effectiveness of BNT162b2 Covid-19 vaccine in preventing SARS-CoV-2 infection in healthcare personnel in six Israeli hospitals (CoVEHPI)

  • Mark A. Katz
  • , Efrat Bron Harlev
  • , Bibiana Chazan
  • , Michal Chowers
  • , David Greenberg
  • , Alon Peretz
  • , Sagi Tshori
  • , Joseph Levy
  • , Mili Yacobi
  • , Avital Hirsch
  • , Doron Amichay
  • , Ronit Weinberger
  • , Anat Ben Dor
  • , Elena Keren Taraday
  • , Dana Reznik
  • , Chen Barazani Chayat
  • , Dana Sagas
  • , Haim Ben Zvi
  • , Rita Berdinstein
  • , Gloria Rashid
  • Yonat Shemer Avni, Michal Mandelboim, Neta Zuckerman, Nir Rainy, Amichay Akriv, Noa Dagan, Eldad Kepten, Noam Barda, Ran D. Balicer

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Methodologically rigorous studies on Covid-19 vaccine effectiveness (VE) in preventing SARS-CoV-2 infection are critically needed to inform national and global policy on Covid-19 vaccine use. In Israel, healthcare personnel (HCP) were initially prioritized for Covid-19 vaccination, creating an ideal setting to evaluate early real-world VE in a closely monitored population. Methods: We conducted a prospective study among HCP in 6 hospitals to estimate the effectiveness of the BNT162b2 mRNA Covid-19 vaccine in preventing SARS-CoV-2 infection. Participants filled out weekly symptom questionnaires, provided weekly nasal specimens, and three serology samples – at enrollment, 30 days and 90 days. We estimated VE against PCR-confirmed SARS-CoV-2 infection using the Cox Proportional Hazards model and against a combined PCR/serology endpoint using Fisher's exact test. Results: Of the 1567 HCP enrolled between December 27, 2020 and February 15, 2021, 1250 previously uninfected participants were included in the primary analysis; 998 (79.8%) were vaccinated with their first dose prior to or at enrollment, all with Pfizer BNT162b2 mRNA vaccine. There were four PCR-positive events among vaccinated participants, and nine among unvaccinated participants. Adjusted two-dose VE against any PCR-confirmed infection was 94.5% (95% CI: 82.6%-98.2%); adjusted two-dose VE against a combined endpoint of PCR and seroconversion for a 60-day follow-up period was 94.5% (95% CI: 63.0%-99.0%). Five PCR-positive samples from study participants were sequenced; all were alpha variant. Conclusions: Our prospective VE study of HCP in Israel with rigorous weekly surveillance found very high VE for two doses of Pfizer BNT162b2 mRNA vaccine against SARS-CoV-2 infection in recently vaccinated HCP during a period of predominant alpha variant circulation. Funding: Clalit Health Services.

Original languageEnglish
Pages (from-to)512-520
Number of pages9
JournalVaccine
Volume40
Issue number3
DOIs
StatePublished - 24 Jan 2022
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2021 Elsevier Ltd

ASJC Scopus subject areas

  • Molecular Medicine
  • General Immunology and Microbiology
  • General Veterinary
  • Public Health, Environmental and Occupational Health
  • Infectious Diseases

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