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Duration of mRNA vaccine protection against SARS-CoV-2 Omicron BA.1 and BA.2 subvariants in Qatar.

Hiam ChemaitellyHoussein H AyoubSawsan AlMukdadPeter CoylePatrick TangHadi Mohamad YassineHebah A Al-KhatibMaria K SmattiMohammad R HasanZaina Al-KanaaniEinas Al-KuwariAndrew M JeremijenkoAnvar Hassan KaleeckalAli Nizar LatifRiyazuddin Mohammad ShaikHanan F Abdul-RahimGheyath K NasrallahMohamed Ghaith Al-KuwariAdeel Ajwad ButtHamad Eid Al-RomaihiMohamed H Al-ThaniAbdullatif Al-KhalRoberto BertolliniLaith Jamal Abu-Raddad
Published in: Nature communications (2022)
SARS-CoV-2 Omicron BA.1 and BA.2 subvariants are genetically divergent. We conducted a matched, test-negative, case-control study to estimate duration of protection of the second and third/booster doses of mRNA COVID-19 vaccines against BA.1 and BA.2 infections in Qatar. BNT162b2 effectiveness was highest at 46.6% (95% CI: 33.4-57.2%) against symptomatic BA.1 and at 51.7% (95% CI: 43.2-58.9%) against symptomatic BA.2 infections in the first three months after the second dose, but declined to ~10% or below thereafter. Effectiveness rebounded to 59.9% (95% CI: 51.2-67.0%) and 43.7% (95% CI: 36.5-50.0%), respectively, in the first month after the booster dose, before declining again. Effectiveness against COVID-19 hospitalization and death was 70-80% after the second dose and >90% after the booster dose. mRNA-1273 vaccine protection showed similar patterns. mRNA vaccines provide comparable, moderate, and short-lived protection against symptomatic BA.1 and BA.2 Omicron infections, but strong and durable protection against COVID-19 hospitalization and death.
Keyphrases
  • sars cov
  • coronavirus disease
  • randomized controlled trial
  • systematic review
  • respiratory syndrome coronavirus