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10.1016/S1474-4422(08)70117-0 Lancet 125 HeikkilaR
When considering authorizing the updated booster, the FDA said it looked at immune response data from adults who had received the original booster, which targeted the original omicron variant BA.1, as well data from a study comparing children who received the original booster and children who only received the primary series
3), a post-translational modification where N-acetylglucosamine is added to serine 529, relieving the activation by fructose-2,6-bisphosphate 103
