Effectiveness of BNT162b2 mRNA COVID-19 vaccine against SARS-CoV-2 variant Beta (B.1.351) among persons identified through contact tracing in Israel: A prospective cohort study.

COVID-19 SARS-CoV-2 epidemiology mRNA vaccines prevention vaccine effectiveness variant Beta (B.1.351)

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 08 09 2021
revised: 19 10 2021
accepted: 20 10 2021
entrez: 6 12 2021
pubmed: 7 12 2021
medline: 7 12 2021
Statut: ppublish

Résumé

SARS-CoV-2 variant Beta (B.1.351) was designated as a Variant of Concern (VoC) after becoming the dominant strain in South Africa and spreading internationally. BNT162b2 showed lower levels of neutralizing antibodies against Beta than against other strains raising concerns about effectiveness of vaccines against infections caused by Beta. We estimated BNT162b2 vaccine effectiveness (VE) against Beta infections in Israel, a country with high vaccine uptake. The Ministry of Health (MoH) identified Beta cases through mandatory reporting of SARS-CoV-2 cases and whole genome sequencing (WGS) of specimens from vaccination-breakthrough infections, reinfections, arriving international travelers, and a selection of other infected persons. A cohort analysis was conducted of exposure events of contacts of primary Beta cases. WGS was conducted on available PCR-positive specimens collected from contacts. VE estimates with 95% confidence intervals (CIs) against confirmed and probable Beta infections were determined by comparing infection risk between unvaccinated and fully-vaccinated (≥7 days after the second dose) contacts, and between unvaccinated and partially-vaccinated (<7 days after the second dose) contacts. MoH identified 310 Beta cases through Jun 27, 2021. During the study period (Dec 11, 2020 - Mar 25, 2021), 164 non-institutionalized primary Beta cases, with 552 contacts aged ≥16 years, were identified. 343/552 (62%) contacts were interviewed and tested. 71/343 (21%) contacts were PCR-positive. WGS was performed on 7/71 (10%) PCR-positive specimens; all were Beta. Among SARS-CoV-2-infected contacts, 48/71 (68%) were symptomatic, 10/71 (14%) hospitalized, and 2/71 (3%) died. Fully-vaccinated VE against confirmed or probable Beta infections was 72% (95% CI -5 - 97%; p=0·04) and against symptomatic confirmed or probable Beta infections was 100% (95% CI 19 - 100%; p=0·01). There was no evidence of protection in partially-vaccinated contacts. In a prospective observational study, two doses of BNT162b2 were effective against confirmed and probable Beta infections. Through the end of June 2021, introductions of Beta did not interrupt control of the pandemic in Israel. Israel Ministry of Health and Pfizer.

Sections du résumé

BACKGROUND BACKGROUND
SARS-CoV-2 variant Beta (B.1.351) was designated as a Variant of Concern (VoC) after becoming the dominant strain in South Africa and spreading internationally. BNT162b2 showed lower levels of neutralizing antibodies against Beta than against other strains raising concerns about effectiveness of vaccines against infections caused by Beta. We estimated BNT162b2 vaccine effectiveness (VE) against Beta infections in Israel, a country with high vaccine uptake.
METHODS METHODS
The Ministry of Health (MoH) identified Beta cases through mandatory reporting of SARS-CoV-2 cases and whole genome sequencing (WGS) of specimens from vaccination-breakthrough infections, reinfections, arriving international travelers, and a selection of other infected persons. A cohort analysis was conducted of exposure events of contacts of primary Beta cases. WGS was conducted on available PCR-positive specimens collected from contacts. VE estimates with 95% confidence intervals (CIs) against confirmed and probable Beta infections were determined by comparing infection risk between unvaccinated and fully-vaccinated (≥7 days after the second dose) contacts, and between unvaccinated and partially-vaccinated (<7 days after the second dose) contacts.
FINDINGS RESULTS
MoH identified 310 Beta cases through Jun 27, 2021. During the study period (Dec 11, 2020 - Mar 25, 2021), 164 non-institutionalized primary Beta cases, with 552 contacts aged ≥16 years, were identified. 343/552 (62%) contacts were interviewed and tested. 71/343 (21%) contacts were PCR-positive. WGS was performed on 7/71 (10%) PCR-positive specimens; all were Beta. Among SARS-CoV-2-infected contacts, 48/71 (68%) were symptomatic, 10/71 (14%) hospitalized, and 2/71 (3%) died. Fully-vaccinated VE against confirmed or probable Beta infections was 72% (95% CI -5 - 97%; p=0·04) and against symptomatic confirmed or probable Beta infections was 100% (95% CI 19 - 100%; p=0·01). There was no evidence of protection in partially-vaccinated contacts.
INTERPRETATION CONCLUSIONS
In a prospective observational study, two doses of BNT162b2 were effective against confirmed and probable Beta infections. Through the end of June 2021, introductions of Beta did not interrupt control of the pandemic in Israel.
FUNDING BACKGROUND
Israel Ministry of Health and Pfizer.

Identifiants

pubmed: 34870134
doi: 10.1016/j.eclinm.2021.101190
pii: S2589-5370(21)00471-5
pmc: PMC8628463
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101190

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

Frederick Angulo, David Swerdlow, John McLaughlin, Farid Khan, Gabriel Mircus, Kaijie Pan, Jo Southern, and Luis Jodar are employees of Pfizer Inc, and hold stock and stock options in Pfizer Inc. Marc Lipsitch has provided advice on COVID-19 free of charge to Janssen, Astra-Zeneca, Pfizer, and COVAXX (United Biomedical), as well as to the nonprofit One Day Sooner and has received consulting income or honoraria from Merck, Pfizer, Bristol Meyers Squibb, Janssen, and Sanofi, and institutional research support from Pfizer. He is on the Scientific Advisory Committee of the Coalition for Epidemic Preparedness and Innovations (CEPI). All other authors report no conflicts.

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Auteurs

Shepherd R Singer (SR)

Public Health Services, Israel Ministry of Health, Jerusalem, Israel.
Hadassah Braun School of Public Health, Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Frederick J Angulo (FJ)

Pfizer Inc., Collegeville, PA, USA.

David L Swerdlow (DL)

Pfizer Inc., Collegeville, PA, USA.

John M McLaughlin (JM)

Pfizer Inc., Collegeville, PA, USA.

Itay Hazan (I)

Ministry of Defense, Tel Aviv, Israel.

Netanel Ginish (N)

Ministry of Defense, Tel Aviv, Israel.

Emilia Anis (E)

Public Health Services, Israel Ministry of Health, Jerusalem, Israel.
Hadassah Braun School of Public Health, Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Ella Mendelson (E)

Central Virology Laboratory, Sheba Medical Center, Ramat Gan, Israel.
School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Orna Mor (O)

Central Virology Laboratory, Sheba Medical Center, Ramat Gan, Israel.
School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Neta S Zuckerman (NS)

Central Virology Laboratory, Sheba Medical Center, Ramat Gan, Israel.
School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Oran Erster (O)

Central Virology Laboratory, Sheba Medical Center, Ramat Gan, Israel.
School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Jo Southern (J)

Pfizer Inc., Collegeville, PA, USA.

Kaijie Pan (K)

Pfizer Inc., Collegeville, PA, USA.

Gabriel Mircus (G)

Pfizer Pharmaceuticals Israel Ltd, Herzliya, Israel.

Marc Lipsitch (M)

Harvard University, Boston, MA, USA.

Eric J Haas (EJ)

Public Health Services, Israel Ministry of Health, Jerusalem, Israel.
Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.

Luis Jodar (L)

Pfizer Inc., Collegeville, PA, USA.

Yeheskel Levy (Y)

Israel Ministry of Health, Jerusalem, Israel.

Sharon Alroy-Preis (S)

Public Health Services, Israel Ministry of Health, Jerusalem, Israel.

Classifications MeSH