Predicted Symptomatic Effectiveness of Pfizer-BioNTech BNT162b2 Vaccine Against Omicron Variant of SARS-CoV-2

Abstract

AbstractThis paper presents predictions of the symptomatic effectiveness of the Pfizer-BioNTech BNT162b2 (Comirnaty) vaccine against Omicron B.1.1.529, the latest SARS-CoV-2 variant of concern. They were obtained assuming fold decreases in Omicron neutralisation by vaccine-induced antibodies versus neutralisation of the virus Wild Type. A 25-fold decrease was assumed based on Omicron pseudovirus neutralisation study by Pfizer and BioNTech; a 94-fold, based on live-Omicron neutralisation study in South Africa; and 40, 80 and 120 folds, hypothesised based on genetic information. The effectiveness of two vaccine doses was predicted as 66% (42, 86), 48% (25, 72) and 42% (20, 66) for up to five months starting 2-4 weeks after the second dose, for the 25, 80 and 120 folds, respectively. The effectiveness of booster vaccination was predicted under a highly conservative assumption that the third dose would increase neutralisation by only 3.3 folds compared to the second dose. The predictions of effectiveness for up to five months, starting 2-4 weeks after the third dose, were 81% (59, 95), 67% (43, 87) and 61% (37, 82) for the 25, 80 and 120 folds, respectively. Despite the large fold decreases considered, the vaccine could still provide substantial protection, particularly after a booster and against severe disease. The paper is accompanied by free software which can be used to predict the symptomatic effectiveness of Comirnaty against Omicron under different neutralisation folds, including those obtained experimentally.