| Literature DB >> 34728831 |
Patrick Tang1, Mohammad R Hasan1, Hiam Chemaitelly2,3, Hadi M Yassine4,5, Fatiha M Benslimane4,5, Hebah A Al Khatib4,5, Sawsan AlMukdad2,3, Peter Coyle4,6,7, Houssein H Ayoub8, Zaina Al Kanaani6, Einas Al Kuwari6, Andrew Jeremijenko6, Anvar Hassan Kaleeckal6, Ali Nizar Latif6, Riyazuddin Mohammad Shaik6, Hanan F Abdul Rahim9, Gheyath K Nasrallah4,5, Mohamed Ghaith Al Kuwari10, Hamad Eid Al Romaihi11, Adeel A Butt6,12, Mohamed H Al-Thani11, Abdullatif Al Khal6, Roberto Bertollini11, Laith J Abu-Raddad13,14,15,16.
Abstract
With the global expansion of the highly transmissible SARS-CoV-2 Delta (B.1.617.2) variant, we conducted a matched test-negative case-control study to assess the real-world effectiveness of COVID-19 messenger RNA vaccines against infection with Delta in Qatar's population. BNT162b2 effectiveness against any, symptomatic or asymptomatic, Delta infection was 45.3% (95% CI, 22.0-61.6%) ≥14 d after the first vaccine dose, but only 51.9% (95% CI, 47.0-56.4%) ≥14 d after the second dose, with 50% of fully vaccinated individuals receiving their second dose before 11 May 2021. Corresponding mRNA-1273 effectiveness ≥14 d after the first or second dose was 73.7% (95% CI, 58.1-83.5%) and 73.1% (95% CI, 67.5-77.8%), respectively. Notably, effectiveness against Delta-induced severe, critical or fatal disease was 93.4% (95% CI, 85.4-97.0%) for BNT162b2 and 96.1% (95% CI, 71.6-99.5%) for mRNA-1273 ≥ 14 d after the second dose. Our findings show robust effectiveness for both BNT162b2 and mRNA-1273 in preventing Delta hospitalization and death in Qatar's population, despite lower effectiveness in preventing infection, particularly for the BNT162b2 vaccine.Entities:
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Year: 2021 PMID: 34728831 DOI: 10.1038/s41591-021-01583-4
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440