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2301. Viral Kinetics of Sequential SARS-CoV-2 Infections

BACKGROUND: An estimated 65% of the US population had at least two SARS-CoV-2 infections by November 2022, but the impact of prior infection on disease course in subsequent infections has been debated. Population-level studies can yield conflicting results due to biases that arise from differences i...

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Autores principales: Kissler, Stephen, Hay, James, Fauver, Joseph, Mack, Christina, Tai, Caroline, Anderson, Deverick, Ho, David D, Grubaugh, Nathan, Grad, Yonatan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677142/
http://dx.doi.org/10.1093/ofid/ofad500.1923
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author Kissler, Stephen
Hay, James
Fauver, Joseph
Mack, Christina
Tai, Caroline
Anderson, Deverick
Ho, David D
Grubaugh, Nathan
Grad, Yonatan H
author_facet Kissler, Stephen
Hay, James
Fauver, Joseph
Mack, Christina
Tai, Caroline
Anderson, Deverick
Ho, David D
Grubaugh, Nathan
Grad, Yonatan H
author_sort Kissler, Stephen
collection PubMed
description BACKGROUND: An estimated 65% of the US population had at least two SARS-CoV-2 infections by November 2022, but the impact of prior infection on disease course in subsequent infections has been debated. Population-level studies can yield conflicting results due to biases that arise from differences in differences in infection history, vaccination status, and patient characteristics. Examining the dynamics of SARS-CoV-2 infections at the individual level can help adjust for these biases. METHODS: Using a convenience sample of 94,812 longitudinal RT-qPCR measurements from samples each taken from a combined anterior nares/oropharyngeal swab, we compared the SARS-CoV-2 viral kinetics of first vs. second infections, adjusting for viral variant, vaccination status, and age. We characterized the kinetics of these infections by fitting a hierarchical Bayesian piecewise linear model to the viral concentration measurements. RESULTS: Relative to first infections, second infections usually featured a faster clearance time (5.1 days, 95% CI (4.7, 5.7) vs. 8.8 days (7.8, 9.8) in first infections), especially in individuals who received a vaccine dose between their first and second infection. Furthermore, a person’s relative (rank-order) viral clearance time, compared to others infected with the same variant, was similar across first and second infections (Spearman correlation: 0.475, p < 0.0001); that is, individuals who had a relatively fast clearance time in their first infection tended to also have a relatively fast clearance time in their second infection. CONCLUSION: Like vaccination, immunity from a prior SARS-CoV-2 infection shortens the duration of subsequent acute SARS-CoV-2 infections principally by reducing viral clearance time. Additionally, there appears to be an inherent element of the immune response, or some other host factor, that shapes a person’s relative ability to clear SARS-CoV-2 infection that persists across sequential infections. DISCLOSURES: Stephen Kissler, PhD, ModernaTx: Advisor/Consultant Christina Mack, PhD, IQVIA: Full time employee of IQVIA which is in paid contractual relationship with bio pharma companies. Caroline Tai, PhD, Evidation Health: Stocks/Bonds|IQVIA: Employee Yonatan H. Grad, MD, PhD, Day Zero Diagnostics: Board Member|GSK: Advisor/Consultant
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spelling pubmed-106771422023-11-27 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections Kissler, Stephen Hay, James Fauver, Joseph Mack, Christina Tai, Caroline Anderson, Deverick Ho, David D Grubaugh, Nathan Grad, Yonatan H Open Forum Infect Dis Abstract BACKGROUND: An estimated 65% of the US population had at least two SARS-CoV-2 infections by November 2022, but the impact of prior infection on disease course in subsequent infections has been debated. Population-level studies can yield conflicting results due to biases that arise from differences in differences in infection history, vaccination status, and patient characteristics. Examining the dynamics of SARS-CoV-2 infections at the individual level can help adjust for these biases. METHODS: Using a convenience sample of 94,812 longitudinal RT-qPCR measurements from samples each taken from a combined anterior nares/oropharyngeal swab, we compared the SARS-CoV-2 viral kinetics of first vs. second infections, adjusting for viral variant, vaccination status, and age. We characterized the kinetics of these infections by fitting a hierarchical Bayesian piecewise linear model to the viral concentration measurements. RESULTS: Relative to first infections, second infections usually featured a faster clearance time (5.1 days, 95% CI (4.7, 5.7) vs. 8.8 days (7.8, 9.8) in first infections), especially in individuals who received a vaccine dose between their first and second infection. Furthermore, a person’s relative (rank-order) viral clearance time, compared to others infected with the same variant, was similar across first and second infections (Spearman correlation: 0.475, p < 0.0001); that is, individuals who had a relatively fast clearance time in their first infection tended to also have a relatively fast clearance time in their second infection. CONCLUSION: Like vaccination, immunity from a prior SARS-CoV-2 infection shortens the duration of subsequent acute SARS-CoV-2 infections principally by reducing viral clearance time. Additionally, there appears to be an inherent element of the immune response, or some other host factor, that shapes a person’s relative ability to clear SARS-CoV-2 infection that persists across sequential infections. DISCLOSURES: Stephen Kissler, PhD, ModernaTx: Advisor/Consultant Christina Mack, PhD, IQVIA: Full time employee of IQVIA which is in paid contractual relationship with bio pharma companies. Caroline Tai, PhD, Evidation Health: Stocks/Bonds|IQVIA: Employee Yonatan H. Grad, MD, PhD, Day Zero Diagnostics: Board Member|GSK: Advisor/Consultant Oxford University Press 2023-11-27 /pmc/articles/PMC10677142/ http://dx.doi.org/10.1093/ofid/ofad500.1923 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Kissler, Stephen
Hay, James
Fauver, Joseph
Mack, Christina
Tai, Caroline
Anderson, Deverick
Ho, David D
Grubaugh, Nathan
Grad, Yonatan H
2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title_full 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title_fullStr 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title_full_unstemmed 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title_short 2301. Viral Kinetics of Sequential SARS-CoV-2 Infections
title_sort 2301. viral kinetics of sequential sars-cov-2 infections
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677142/
http://dx.doi.org/10.1093/ofid/ofad500.1923
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