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Immune correlates analysis of a phase 3 trial of the AZD1222 (ChAdOx1 nCoV-19) vaccine.

David BenkeserYouyi FongHolly E JanesElizabeth J KellyIan HirschStephanie SprouleAnn Marie StanleyJill MaaskeTonya VillafanaChristopher R HouchensKaren MartinsLakshmi JayashankarFlora CastellinoVictor AyalaChristos J PetropoulosAndrew LeithDeanne HaugaardBill WebbYiwen LuChenchen YuBhavesh BorateLars W P van der LaanNima S HejaziLindsay N CarppApril K RandhawaMichele P AndrasikJames G KublinMargaret Brewinski IsaacsMamodikoe MakheneTina TongMerlin L RobbLawrence CoreyKathleen M NeuzilDean FollmannCorey HoffmanAnn R FalseyMagdalena SobieszczykRichard A KoupRuben O DonisPeter B Gilbertnull nullnull nullnull null
Published in: NPJ vaccines (2023)
In the phase 3 trial of the AZD1222 (ChAdOx1 nCoV-19) vaccine conducted in the U.S., Chile, and Peru, anti-spike binding IgG concentration (spike IgG) and pseudovirus 50% neutralizing antibody titer (nAb ID50) measured four weeks after two doses were assessed as correlates of risk and protection against PCR-confirmed symptomatic SARS-CoV-2 infection (COVID-19). These analyses of SARS-CoV-2 negative participants were based on case-cohort sampling of vaccine recipients (33 COVID-19 cases by 4 months post dose two, 463 non-cases). The adjusted hazard ratio of COVID-19 was 0.32 (95% CI: 0.14, 0.76) per 10-fold increase in spike IgG concentration and 0.28 (0.10, 0.77) per 10-fold increase in nAb ID50 titer. At nAb ID50 below the limit of detection (< 2.612 IU50/ml), 10, 100, and 270 IU50/ml, vaccine efficacy was -5.8% (-651%, 75.6%), 64.9% (56.4%, 86.9%), 90.0% (55.8%, 97.6%) and 94.2% (69.4%, 99.1%). These findings provide further evidence towards defining an immune marker correlate of protection to help guide regulatory/approval decisions for COVID-19 vaccines.
Keyphrases
  • sars cov
  • coronavirus disease
  • respiratory syndrome coronavirus
  • advanced non small cell lung cancer
  • binding protein