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Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 lineages circulating in Brazil.

Authors :
Clemens, Sue Ann Costa
Folegatti, Pedro M.
Emary, Katherine R. W.
Weckx, Lily Yin
Ratcliff, Jeremy
Bibi, Sagida
De Almeida Mendes, Ana Verena
Milan, Eveline Pipolo
Pittella, Ana
Schwarzbold, Alexandre V.
Sprinz, Eduardo
Aley, Parvinder K.
Bonsall, David
Fraser, Christophe
Fuskova, Michelle
Gilbert, Sarah C.
Jenkin, Daniel
Kelly, Sarah
Kerridge, Simon
Lambe, Teresa
Source :
Nature Communications; 10/6/2021, Vol. 12 Issue 1, p1-10, 10p
Publication Year :
2021

Abstract

Several COVID-19 vaccines have shown good efficacy in clinical trials, but there remains uncertainty about the efficacy of vaccines against different variants. Here, we investigate the efficacy of ChAdOx1 nCoV-19 (AZD1222) against symptomatic COVID-19 in a post-hoc exploratory analysis of a Phase 3 randomised trial in Brazil (trial registration ISRCTN89951424). Nose and throat swabs were tested by PCR in symptomatic participants. Sequencing and genotyping of swabs were performed to determine the lineages of SARS-CoV-2 circulating during the study. Protection against any symptomatic COVID-19 caused by the Zeta (P.2) variant was assessed in 153 cases with vaccine efficacy (VE) of 69% (95% CI 55, 78). 49 cases of B.1.1.28 occurred and VE was 73% (46, 86). The Gamma (P.1) variant arose later in the trial and fewer cases (N = 18) were available for analysis. VE was 64% (−2, 87). ChAdOx1 nCoV-19 provided 95% protection (95% CI 61%, 99%) against hospitalisation due to COVID-19. In summary, we report that ChAdOx1 nCoV-19 protects against emerging variants in Brazil despite the presence of the spike protein mutation E484K. Emerging variants of SARS-CoV-2 raise concerns about vaccine efficiency. Here, the authors present a post-hoc analysis for the ChAdOx1 nCoV-19 (AZD1222) vaccine trial in Brazil and provide efficacy against symptomatic COVID-19 caused by the Zeta (P.2) and other variants. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
12
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
152852752
Full Text :
https://doi.org/10.1038/s41467-021-25982-w