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Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases

Understanding the risk factors for breakthrough coronavirus disease 2019 (COVID-19) (BC19) is critical to inform policy. Herein, we assessed Delta (Lineage B.1.617.2) variant-specific effectiveness of the BNT162b2 (Pfizer) vaccine and characterized Delta-driven BC19 cases (fully vaccinated individua...

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Autores principales: Vu, Luan D, Wallace, Shonta, Phan, Anh TQ, Christofferson, Rebecca C, Turner, Erik, Parker, Sean, Elkind-Hirsch, Karen, Landry, Darrell, Stansbury, Austin, Rose, Rebecca, Nolan, David J, Lamers, Susanna L, Hirezi, Michael, Ogden, Beverly, Cormier, Stephania A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679329/
https://www.ncbi.nlm.nih.gov/pubmed/36408542
http://dx.doi.org/10.1177/15353702221134097
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author Vu, Luan D
Wallace, Shonta
Phan, Anh TQ
Christofferson, Rebecca C
Turner, Erik
Parker, Sean
Elkind-Hirsch, Karen
Landry, Darrell
Stansbury, Austin
Rose, Rebecca
Nolan, David J
Lamers, Susanna L
Hirezi, Michael
Ogden, Beverly
Cormier, Stephania A
author_facet Vu, Luan D
Wallace, Shonta
Phan, Anh TQ
Christofferson, Rebecca C
Turner, Erik
Parker, Sean
Elkind-Hirsch, Karen
Landry, Darrell
Stansbury, Austin
Rose, Rebecca
Nolan, David J
Lamers, Susanna L
Hirezi, Michael
Ogden, Beverly
Cormier, Stephania A
author_sort Vu, Luan D
collection PubMed
description Understanding the risk factors for breakthrough coronavirus disease 2019 (COVID-19) (BC19) is critical to inform policy. Herein, we assessed Delta (Lineage B.1.617.2) variant-specific effectiveness of the BNT162b2 (Pfizer) vaccine and characterized Delta-driven BC19 cases (fully vaccinated individuals who get infected) with known-time-since-vaccination. In this longitudinal prospective study (January 21–October 30, 2021), 90 naïve and 15 convalescent individuals were enrolled at the initiation of vaccination. Samples from 27 unvaccinated individuals with previous laboratory-confirmed COVID-19 diagnosis were collected at a single time point. Longitudinal serology profile (antibodies against severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] S and N proteins) and live-virus-based neutralization capacities were assessed while controlling for age. Sex, age, history of reactions to the COVID-19 vaccine, and viral neutralization capacities were identified as significant risk factors for breakthrough COVID-19. At 8 months postvaccination, male sex, individuals ⩾65 years of age, and individuals who experienced noticeable side effects with the COVID-19 vaccine were at 5.47 (p-value = 0.0102), 4.33 (p-value = 0.0236), and 4.95 (p-value = 0.0159) fold greater risk of BC19 as compared to their peers, respectively. Importantly, every five-fold increase in viral neutralization capacities (by live-virus-based assays) was significantly associated with ~4-fold reduction in the risk occurrence of breakthrough COVID-19 (p-value = 0.045). Vaccine boosting remarkably increased these viral neutralization capacities by 16.22-fold (p- value = 0.0005), supporting the importance of the BNT162b2 booster in efforts to control the incursion of future variants into the population at large. Strikingly, BC19 cases exhibited a delayed/absent antibody response to the N protein, suggesting limited exposure to the virus. Since antibodies against N protein are widely used to evaluate the extent of virus spread in communities, our finding has important implications on the utility of existing serological diagnostic and surveillance for COVID-19.
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spelling pubmed-96793292022-11-22 Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases Vu, Luan D Wallace, Shonta Phan, Anh TQ Christofferson, Rebecca C Turner, Erik Parker, Sean Elkind-Hirsch, Karen Landry, Darrell Stansbury, Austin Rose, Rebecca Nolan, David J Lamers, Susanna L Hirezi, Michael Ogden, Beverly Cormier, Stephania A Exp Biol Med (Maywood) Original Research Understanding the risk factors for breakthrough coronavirus disease 2019 (COVID-19) (BC19) is critical to inform policy. Herein, we assessed Delta (Lineage B.1.617.2) variant-specific effectiveness of the BNT162b2 (Pfizer) vaccine and characterized Delta-driven BC19 cases (fully vaccinated individuals who get infected) with known-time-since-vaccination. In this longitudinal prospective study (January 21–October 30, 2021), 90 naïve and 15 convalescent individuals were enrolled at the initiation of vaccination. Samples from 27 unvaccinated individuals with previous laboratory-confirmed COVID-19 diagnosis were collected at a single time point. Longitudinal serology profile (antibodies against severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] S and N proteins) and live-virus-based neutralization capacities were assessed while controlling for age. Sex, age, history of reactions to the COVID-19 vaccine, and viral neutralization capacities were identified as significant risk factors for breakthrough COVID-19. At 8 months postvaccination, male sex, individuals ⩾65 years of age, and individuals who experienced noticeable side effects with the COVID-19 vaccine were at 5.47 (p-value = 0.0102), 4.33 (p-value = 0.0236), and 4.95 (p-value = 0.0159) fold greater risk of BC19 as compared to their peers, respectively. Importantly, every five-fold increase in viral neutralization capacities (by live-virus-based assays) was significantly associated with ~4-fold reduction in the risk occurrence of breakthrough COVID-19 (p-value = 0.045). Vaccine boosting remarkably increased these viral neutralization capacities by 16.22-fold (p- value = 0.0005), supporting the importance of the BNT162b2 booster in efforts to control the incursion of future variants into the population at large. Strikingly, BC19 cases exhibited a delayed/absent antibody response to the N protein, suggesting limited exposure to the virus. Since antibodies against N protein are widely used to evaluate the extent of virus spread in communities, our finding has important implications on the utility of existing serological diagnostic and surveillance for COVID-19. SAGE Publications 2022-11-19 2022-11 /pmc/articles/PMC9679329/ /pubmed/36408542 http://dx.doi.org/10.1177/15353702221134097 Text en © 2022 by the Society for Experimental Biology and Medicine
spellingShingle Original Research
Vu, Luan D
Wallace, Shonta
Phan, Anh TQ
Christofferson, Rebecca C
Turner, Erik
Parker, Sean
Elkind-Hirsch, Karen
Landry, Darrell
Stansbury, Austin
Rose, Rebecca
Nolan, David J
Lamers, Susanna L
Hirezi, Michael
Ogden, Beverly
Cormier, Stephania A
Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title_full Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title_fullStr Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title_full_unstemmed Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title_short Absence of antibody responses to SARS-CoV-2 N protein in COVID-19 vaccine breakthrough cases
title_sort absence of antibody responses to sars-cov-2 n protein in covid-19 vaccine breakthrough cases
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679329/
https://www.ncbi.nlm.nih.gov/pubmed/36408542
http://dx.doi.org/10.1177/15353702221134097
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