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DOI 10.1093/cid/ciac290

Медицинская библиотека · Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022

Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada.

Skowronski Danuta M, Febriani Yossi, Ouakki Manale, Setayeshgar Solmaz, El Adam Shiraz, Zou Macy, Talbot Denis, Prystajecky Natalie, Tyson John R, Gilca Rodica, Brousseau Nicholas, Deceuninck Geneviève, Galanis Eleni, Fjell Chris D, Sbihi Hind, Fortin Elise, Barkati Sapha, Sauvageau Chantal, Naus Monika, Patrick David M, Henry Bonnie, Hoang Linda M N, De Wals Philippe, Garenc Christophe, Carignan Alex, Drolet Mélanie, Jassem Agatha N, Sadarangani Manish, Brisson Marc, Krajden Mel, De Serres Gaston

СтатьяПоддержка службы здравоохранения СШАПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

The Canadian coronavirus disease 2019 (COVID-19) immunization strategy deferred second doses and allowed mixed schedules. We compared 2-dose vaccine effectiveness (VE) by vaccine type (mRNA and/or ChAdOx1), interval between doses, and time since second dose in 2 of Canada's larger provinces.

METHODS

Two-dose VE against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or hospitalization among adults ≥18 years, including due to Alpha, Gamma, and Delta variants of concern (VOCs), was assessed ≥14 days postvaccination by test-negative design studies separately conducted in British Columbia and Quebec, Canada, between 30 May and 27 November (epi-weeks 22-47) 2021.

RESULTS

In both provinces, all homologous or heterologous mRNA and/or ChAdOx1 2-dose schedules were associated with ≥90% reduction in SARS-CoV-2 hospitalization risk for ≥7 months. With slight decline from a peak of >90%, VE against infection was ≥80% for ≥6 months following homologous mRNA vaccination, lower by ∼10% when both doses were ChAdOx1 but comparably high following heterologous ChAdOx1 + mRNA receipt. Findings were similar by age group, sex, and VOC. VE was significantly higher with longer 7-8-week versus manufacturer-specified 3-4-week intervals between mRNA doses.

CONCLUSIONS

Two doses of any mRNA and/or ChAdOx1 combination gave substantial and sustained protection against SARS-CoV-2 hospitalization, spanning Delta-dominant circulation. ChAdOx1 VE against infection was improved by heterologous mRNA series completion. A 7-8-week interval between first and second doses improved mRNA VE and may be the optimal schedule outside periods of intense epidemic surge. Findings support interchangeability and extended intervals between SARS-CoV-2 vaccine doses, with potential global implications for low-coverage areas and, going forward, for children.

Для цитирования: Skowronski Danuta M, Febriani Yossi, Ouakki Manale, Setayeshgar Solmaz, El Adam Shiraz, Zou Macy, Talbot Denis, Prystajecky Natalie, Tyson John R, Gilca Rodica, Brousseau Nicholas, Deceuninck Geneviève, Galanis Eleni, Fjell Chris D, Sbihi Hind, Fortin Elise, Barkati Sapha, Sauvageau Chantal, Naus Monika, Patrick David M, Henry Bonnie, Hoang Linda M N, De Wals Philippe, Garenc Christophe, Carignan Alex, Drolet Mélanie, Jassem Agatha N, Sadarangani Manish, Brisson Marc, Krajden Mel, De Serres Gaston. Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada.. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2022. DOI: 10.1093/cid/ciac290.

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