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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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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 |
format | Online Article Text |
id | pubmed-10677142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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