Protective Duration of ChAdOx1 and BNT162b2 Vaccines Against SARS-CoV-2 Infection.


Journal

Clinical drug investigation
ISSN: 1179-1918
Titre abrégé: Clin Drug Investig
Pays: New Zealand
ID NLM: 9504817

Informations de publication

Date de publication:
Oct 2022
Historique:
accepted: 16 08 2022
pubmed: 31 8 2022
medline: 12 10 2022
entrez: 30 8 2022
Statut: ppublish

Résumé

A limited number of studies have addressed the protective duration of coronavirus disease 2019 (COVID-19) vaccines following primary and booster doses in Saudi Arabia. Therefore, this study aimed to evaluate the protective duration of primary and booster doses of BNT162b2 and ChAdOx1 COVID-19 vaccine batches in Saudi Arabia. A cross-sectional study was conducted from 1 January to 31 December, 2021. The study included 53,354 people infected with severe acute respiratory syndrome coronavirus-2 2 weeks or more after receiving at least a primary vaccination of either the ChAdOx1 or BNT162b2 vaccine. The total median protective duration of both primary COVID-19 vaccinations was 134 days. Heterologous primary vaccination (ChAdOx1 followed by BNT162b2) showed a significantly higher median protective duration of 142 days. The results show that the total median protective duration of the first booster doses of COVID-19 vaccines was 57 days. ChAdOx1 batch code C1 was found to have the most extended protective duration of 173 days (range 163-192 days). The current study revealed that the median protective duration of ChAdOx1 and BNT162b2 COVID-19 primary vaccination regimens administered in Saudi Arabia in 2021 was 134 days and that heterologous primary vaccination (ChAdOx1→BNT162b2) exhibited a significantly higher protective duration than other vaccination regimens.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
A limited number of studies have addressed the protective duration of coronavirus disease 2019 (COVID-19) vaccines following primary and booster doses in Saudi Arabia. Therefore, this study aimed to evaluate the protective duration of primary and booster doses of BNT162b2 and ChAdOx1 COVID-19 vaccine batches in Saudi Arabia.
METHODS METHODS
A cross-sectional study was conducted from 1 January to 31 December, 2021. The study included 53,354 people infected with severe acute respiratory syndrome coronavirus-2 2 weeks or more after receiving at least a primary vaccination of either the ChAdOx1 or BNT162b2 vaccine.
RESULTS RESULTS
The total median protective duration of both primary COVID-19 vaccinations was 134 days. Heterologous primary vaccination (ChAdOx1 followed by BNT162b2) showed a significantly higher median protective duration of 142 days. The results show that the total median protective duration of the first booster doses of COVID-19 vaccines was 57 days. ChAdOx1 batch code C1 was found to have the most extended protective duration of 173 days (range 163-192 days).
CONCLUSIONS CONCLUSIONS
The current study revealed that the median protective duration of ChAdOx1 and BNT162b2 COVID-19 primary vaccination regimens administered in Saudi Arabia in 2021 was 134 days and that heterologous primary vaccination (ChAdOx1→BNT162b2) exhibited a significantly higher protective duration than other vaccination regimens.

Identifiants

pubmed: 36040662
doi: 10.1007/s40261-022-01195-x
pii: 10.1007/s40261-022-01195-x
pmc: PMC9425807
doi:

Substances chimiques

COVID-19 Vaccines 0
ChAdOx1 nCoV-19 B5S3K2V0G8
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

799-806

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Auteurs

Amjad Alfaleh (A)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia. amfalfaleh@moh.gov.sa.

Abdullah Alkattan (A)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia. abdullahalkattan@gmail.com.

Abrar Alzaher (A)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia.

Nashwa Radwan (N)

Department of Research, Assisting Deputyship for Primary Health Care, Ministry of Heath, Riyadh, Saudi Arabia.
Department of Public Health and Community Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.

Nagla Mahmoud (N)

Department of Research, Assisting Deputyship for Primary Health Care, Ministry of Heath, Riyadh, Saudi Arabia.

Alaa Alageel (A)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia.

Dina Alhabib (D)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia.

Eman Alsalameen (E)

Department of Pharmacy, King Khalid University Hospital, Medical City King Saud University, Riyadh, Saudi Arabia.

Khlood Sagor (K)

Research and Planning Unit, General Directorate of School Health, Ministry of Health, Riyadh, 11176, Saudi Arabia.

Alhan Haji (A)

Department of Research, Assisting Deputyship for Primary Health Care, Ministry of Heath, Riyadh, Saudi Arabia.

Amal Alfaifi (A)

Department of Research, Assisting Deputyship for Primary Health Care, Ministry of Heath, Riyadh, Saudi Arabia.

Khaled Alabdulkareem (K)

Department of Research, Assisting Deputyship for Primary Health Care, Ministry of Heath, Riyadh, Saudi Arabia.
Department of Family Medicine, College of Medicine, Al-Imam Mohammad Bin Saud Islamic University, Riyadh, Saudi Arabia.

Mona Ibrahim (M)

Department of Community, Environmental and Occupational Medicine, Faculty of Medicine, Zagazig University, Zagazig, 44519, Egypt. mhhassan@zu.edu.eg.

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