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Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial
Peter B. Gilbert; David C. Montefiori; Adrian McDermott; Youyi Fong; David C. Benkeser; Weiping Deng; Honghong Zhou; Christopher R. Houchens; Karen Martins; Lakshmi Jayashankar; Flora Castellino; Britta Flach; Bob C. Lin; Charlene McDanal; Amanda Eaton; Marcella Sarzotti-Kelsoe; Yiwen Lu; Chenchen Yu; Bhavesh Borate; Lars W. P. van der Laan; Nima Hejazi; Chuong Huynh; Jacqueline Miller; Hana M. El Sahly; Lindsey R. Baden; Mira Baron; Luis De La Cruz; Cynthia Gay; Spyros Kalams; Colleen F. Kelley; Mark Kutner; Michele P. Andrasik; James G. Kublin; Lawrence Corey; Kathleen M. Neuzil; Lindsay N. Carpp; Rolando Pajon; Dean Follmann; Ruben O. Donis; Richard A. Koup; - Immune Assays Team; - Moderna, Inc. Team; - Coronavirus Vaccine Prevention Network (CoVPN)/Coronavirus Efficacy (COVE) Team; - United States Government (USG)/CoVPN Biostatistics Team.
Affiliation
  • Peter B. Gilbert; Fred Hutchinson Cancer Research Center
  • David C. Montefiori; Duke University
  • Adrian McDermott; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Youyi Fong; Fred Hutchinson Cancer Research Center
  • David C. Benkeser; Emory
  • Weiping Deng; Moderna
  • Honghong Zhou; Moderna
  • Christopher R. Houchens; BARDA
  • Karen Martins; HHS
  • Lakshmi Jayashankar; BARDA
  • Flora Castellino; BARDA
  • Britta Flach; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Bob C. Lin; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Charlene McDanal; Duke University
  • Amanda Eaton; Duke University
  • Marcella Sarzotti-Kelsoe; Duke University
  • Yiwen Lu; Fred Hutchinson Cancer Research Center
  • Chenchen Yu; Fred Hutchinson Cancer Research Center
  • Bhavesh Borate; Fred Hutchinson Cancer Research Center
  • Lars W. P. van der Laan; Fred Hutchinson Cancer Research Center
  • Nima Hejazi; University of Berkeley
  • Chuong Huynh; BARDA
  • Jacqueline Miller; Moderna, Inc.
  • Hana M. El Sahly; Baylor College of Medicine
  • Lindsey R. Baden; Brigham and Women's Hospital
  • Mira Baron; Palm Beach Research Center
  • Luis De La Cruz; Keystone Vitalink Research
  • Cynthia Gay; UNC-Chapel Hill
  • Spyros Kalams; Vanderbilt University Medical Center
  • Colleen F. Kelley; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine and the Grady Health System
  • Mark Kutner; Suncoast Research Group
  • Michele P. Andrasik; Fred Hutchinson Cancer Research Center
  • James G. Kublin; Fred Hutchinson Cancer Research Center
  • Lawrence Corey; Fred Hutchinson Cancer Research Center
  • Kathleen M. Neuzil; University of Maryland School of Medicine
  • Lindsay N. Carpp; Fred Hutchinson Cancer Research Center
  • Rolando Pajon; Moderna, Inc.
  • Dean Follmann; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Ruben O. Donis; BARDA
  • Richard A. Koup; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • - Immune Assays Team;
  • - Moderna, Inc. Team;
  • - Coronavirus Vaccine Prevention Network (CoVPN)/Coronavirus Efficacy (COVE) Team;
  • - United States Government (USG)/CoVPN Biostatistics Team;
Preprint in English | medRxiv | ID: ppmedrxiv-21261290
ABSTRACT
BackgroundIn the Coronavirus Efficacy (COVE) trial, estimated mRNA-1273 vaccine efficacy against coronavirus disease-19 (COVID-19) was 94%. SARS-CoV-2 antibody measurements were assessed as correlates of COVID-19 risk and as correlates of protection. MethodsThrough case-cohort sampling, participants were selected for measurement of four serum antibody markers at Day 1 (first dose), Day 29 (second dose), and Day 57 IgG binding antibodies (bAbs) to Spike, bAbs to Spike receptor-binding domain (RBD), and 50% and 80% inhibitory dilution pseudovirus neutralizing antibody titers calibrated to the WHO International Standard (cID50 and cID80). Participants with no evidence of previous SARS-CoV-2 infection were included. Cox regression assessed in vaccine recipients the association of each Day 29 or 57 serologic marker with COVID-19 through 126 or 100 days of follow-up, respectively, adjusting for risk factors. ResultsDay 57 Spike IgG, RBD IgG, cID50, and cID80 neutralization levels were each inversely correlated with risk of COVID-19 hazard ratios 0.66 (95% CI 0.50, 0.88; p=0.005); 0.57 (0.40, 0.82; p=0.002); 0.42 (0.27, 0.65; p<0.001); 0.35 (0.20, 0.61; p<0.001) per 10-fold increase in marker level, respectively, multiplicity adjusted P-values 0.003-0.010. Results were similar for Day 29 markers (multiplicity adjusted P-values <0.001-0.003). For vaccine recipients with Day 57 reciprocal cID50 neutralization titers that were undetectable (<2.42), 100, or 1000, respectively, cumulative incidence of COVID-19 through 100 days post Day 57 was 0.030 (0.010, 0.093), 0.0056 (0.0039, 0.0080), and 0.0023 (0.0013, 0.0036). For vaccine recipients at these titer levels, respectively, vaccine efficacy was 50.8% (-51.2, 83.0%), 90.7% (86.7, 93.6%), and 96.1% (94.0, 97.8%). Causal mediation analysis estimated that the proportion of vaccine efficacy mediated through Day 29 cID50 titer was 68.5% (58.5, 78.4%). ConclusionsBinding and neutralizing antibodies correlated with COVID-19 risk and vaccine efficacy and likely have utility in predicting mRNA-1273 vaccine efficacy against COVID-19. Trial registration numberCOVE ClinicalTrials.gov number, NCT04470427
License
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study / Rct Language: English Year: 2021 Document type: Preprint
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