Population-Based Evaluation of Vaccine Effectiveness against SARS-CoV-2 Infection, Severe Illness, and Death, Taiwan

Emerg Infect Dis. 2024 Mar;30(3):478-489. doi: 10.3201/eid3003.230893. Epub 2024 Jan 31.

Abstract

Taiwan provided several COVID-19 vaccine platforms: mRNA (BNT162b2, mRNA-1273), adenoviral vector-based (AZD1222), and protein subunit (MVC-COV1901). After Taiwan shifted from its zero-COVID strategy in April 2022, population-based evaluation of vaccine effectiveness (VE) became possible. We conducted an observational cohort study of 21,416,151 persons to examine VE against SARS-CoV-2 infection, moderate and severe illness, and death during March 22, 2021-September 30, 2022. After adjusting for age and sex, we found that persons who completed 3 vaccine doses (2 primary, 1 booster) or received MVC-COV1901 as the primary series had the lowest hospitalization incidence (0.04-0.20 cases/100,000 person-days). We also found 95.8% VE against hospitalization for 3 doses of BNT162b2, 91.0% for MVC-COV1901, 81.8% for mRNA-1273, and 65.7% for AZD1222, which had the lowest overall VE. Our findings indicated that protein subunit vaccines provide similar protection against SARS-CoV-2---associated hospitalization as mRNA vaccines and can inform mix-and-match vaccine selection in other countries.

Keywords: AZD1222; BNT162b2; COVID-19; MVC-COV1901; SARS; SARS-CoV-2; Taiwan; coronavirus; coronavirus disease; mRNA-1273; mix-and-match; population-based cohort study; respiratory infections; severe acute respiratory syndrome coronavirus 2; vaccine effectiveness; viruses; zoonoses.

Publication types

  • Observational Study

MeSH terms

  • 2019-nCoV Vaccine mRNA-1273
  • BNT162 Vaccine
  • COVID-19 Vaccines
  • COVID-19* / epidemiology
  • COVID-19* / prevention & control
  • ChAdOx1 nCoV-19
  • Cohort Studies
  • Female
  • Humans
  • Male
  • SARS-CoV-2 / genetics
  • Taiwan / epidemiology
  • Vaccine Efficacy

Substances

  • 2019-nCoV Vaccine mRNA-1273
  • BNT162 Vaccine
  • ChAdOx1 nCoV-19
  • COVID-19 Vaccines