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Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial
BACKGROUND: In 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. METHODS: Through case-cohort sampling, particip...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366808/ https://www.ncbi.nlm.nih.gov/pubmed/34401888 http://dx.doi.org/10.1101/2021.08.09.21261290 |
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author | Gilbert, Peter B. Montefiori, David C. McDermott, Adrian Fong, Youyi Benkeser, David Deng, Weiping Zhou, Honghong Houchens, Christopher R. Martins, Karen Jayashankar, Lakshmi Castellino, Flora Flach, Britta Lin, Bob C. O’Connell, Sarah McDanal, Charlene Eaton, Amanda Sarzotti-Kelsoe, Marcella Lu, Yiwen Yu, Chenchen Borate, Bhavesh van der Laan, Lars W. P. Hejazi, Nima Huynh, Chuong Miller, Jacqueline El Sahly, Hana M. Baden, Lindsey R. Baron, Mira De La Cruz, Luis Gay, Cynthia Kalams, Spyros Kelley, Colleen F. Kutner, Mark Andrasik, Michele P. Kublin, James G. Corey, Lawrence Neuzil, Kathleen M. Carpp, Lindsay N. Pajon, Rolando Follmann, Dean Donis, Ruben O. Koup, Richard A. |
author_facet | Gilbert, Peter B. Montefiori, David C. McDermott, Adrian Fong, Youyi Benkeser, David Deng, Weiping Zhou, Honghong Houchens, Christopher R. Martins, Karen Jayashankar, Lakshmi Castellino, Flora Flach, Britta Lin, Bob C. O’Connell, Sarah McDanal, Charlene Eaton, Amanda Sarzotti-Kelsoe, Marcella Lu, Yiwen Yu, Chenchen Borate, Bhavesh van der Laan, Lars W. P. Hejazi, Nima Huynh, Chuong Miller, Jacqueline El Sahly, Hana M. Baden, Lindsey R. Baron, Mira De La Cruz, Luis Gay, Cynthia Kalams, Spyros Kelley, Colleen F. Kutner, Mark Andrasik, Michele P. Kublin, James G. Corey, Lawrence Neuzil, Kathleen M. Carpp, Lindsay N. Pajon, Rolando Follmann, Dean Donis, Ruben O. Koup, Richard A. |
author_sort | Gilbert, Peter B. |
collection | PubMed |
description | BACKGROUND: In 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. METHODS: Through 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. RESULTS: Day 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%). CONCLUSIONS: Binding 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 NUMBER: COVE ClinicalTrials.gov number, NCT04470427 |
format | Online Article Text |
id | pubmed-8366808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-83668082021-08-17 Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial Gilbert, Peter B. Montefiori, David C. McDermott, Adrian Fong, Youyi Benkeser, David Deng, Weiping Zhou, Honghong Houchens, Christopher R. Martins, Karen Jayashankar, Lakshmi Castellino, Flora Flach, Britta Lin, Bob C. O’Connell, Sarah McDanal, Charlene Eaton, Amanda Sarzotti-Kelsoe, Marcella Lu, Yiwen Yu, Chenchen Borate, Bhavesh van der Laan, Lars W. P. Hejazi, Nima Huynh, Chuong Miller, Jacqueline El Sahly, Hana M. Baden, Lindsey R. Baron, Mira De La Cruz, Luis Gay, Cynthia Kalams, Spyros Kelley, Colleen F. Kutner, Mark Andrasik, Michele P. Kublin, James G. Corey, Lawrence Neuzil, Kathleen M. Carpp, Lindsay N. Pajon, Rolando Follmann, Dean Donis, Ruben O. Koup, Richard A. medRxiv Article BACKGROUND: In 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. METHODS: Through 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. RESULTS: Day 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%). CONCLUSIONS: Binding 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 NUMBER: COVE ClinicalTrials.gov number, NCT04470427 Cold Spring Harbor Laboratory 2021-08-15 /pmc/articles/PMC8366808/ /pubmed/34401888 http://dx.doi.org/10.1101/2021.08.09.21261290 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Gilbert, Peter B. Montefiori, David C. McDermott, Adrian Fong, Youyi Benkeser, David Deng, Weiping Zhou, Honghong Houchens, Christopher R. Martins, Karen Jayashankar, Lakshmi Castellino, Flora Flach, Britta Lin, Bob C. O’Connell, Sarah McDanal, Charlene Eaton, Amanda Sarzotti-Kelsoe, Marcella Lu, Yiwen Yu, Chenchen Borate, Bhavesh van der Laan, Lars W. P. Hejazi, Nima Huynh, Chuong Miller, Jacqueline El Sahly, Hana M. Baden, Lindsey R. Baron, Mira De La Cruz, Luis Gay, Cynthia Kalams, Spyros Kelley, Colleen F. Kutner, Mark Andrasik, Michele P. Kublin, James G. Corey, Lawrence Neuzil, Kathleen M. Carpp, Lindsay N. Pajon, Rolando Follmann, Dean Donis, Ruben O. Koup, Richard A. Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title | Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title_full | Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title_fullStr | Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title_full_unstemmed | Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title_short | Immune Correlates Analysis of the mRNA-1273 COVID-19 Vaccine Efficacy Trial |
title_sort | immune correlates analysis of the mrna-1273 covid-19 vaccine efficacy trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366808/ https://www.ncbi.nlm.nih.gov/pubmed/34401888 http://dx.doi.org/10.1101/2021.08.09.21261290 |
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