Waning of BNT162b2 Vaccine Protection against SARS-CoV-2 Infection in Qatar.
Waning of BNT162b2 Vaccine Protection against SARS-CoV-2 Infection in Qatar.
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DOI:
10.1056/nejmoa2114114
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发表时间:
2021-12-09
期刊:
影响因子:
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通讯作者:
Abu-Raddad LJ
中科院分区:
文献类型:
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作者:
Chemaitelly H;Tang P;Hasan MR;AlMukdad S;Yassine HM;Benslimane FM;Al Khatib HA;Coyle P;Ayoub HH;Al Kanaani Z;Al Kuwari E;Jeremijenko A;Kaleeckal AH;Latif AN;Shaik RM;Abdul Rahim HF;Nasrallah GK;Al Kuwari MG;Al Romaihi HE;Butt AA;Al-Thani MH;Al Khal A;Bertollini R;Abu-Raddad LJ
Waning of vaccine protection against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or coronavirus disease 2019 (Covid-19) is a concern. The persistence of BNT162b2 (Pfizer–BioNTech) vaccine effectiveness against infection and disease in Qatar, where the B.1.351 (or beta) and B.1.617.2 (or delta) variants have dominated incidence and polymerase-chain-reaction testing is done on a mass scale, is unclear. We used a matched test-negative, case–control study design to estimate vaccine effectiveness against any SARS-CoV-2 infection and against any severe, critical, or fatal case of Covid-19, from January 1 to September 5, 2021. Estimated BNT162b2 effectiveness against any SARS-CoV-2 infection was negligible in the first 2 weeks after the first dose. It increased to 36.8% (95% confidence interval [CI], 33.2 to 40.2) in the third week after the first dose and reached its peak at 77.5% (95% CI, 76.4 to 78.6) in the first month after the second dose. Effectiveness declined gradually thereafter, with the decline accelerating after the fourth month to reach approximately 20% in months 5 through 7 after the second dose. Effectiveness against symptomatic infection was higher than effectiveness against asymptomatic infection but waned similarly. Variant-specific effectiveness waned in the same pattern. Effectiveness against any severe, critical, or fatal case of Covid-19 increased rapidly to 66.1% (95% CI, 56.8 to 73.5) by the third week after the first dose and reached 96% or higher in the first 2 months after the second dose; effectiveness persisted at approximately this level for 6 months. BNT162b2-induced protection against SARS-CoV-2 infection appeared to wane rapidly following its peak after the second dose, but protection against hospitalization and death persisted at a robust level for 6 months after the second dose. (Funded by Weill Cornell Medicine–Qatar and others.)