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How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections?
Acute viral infections pose many practical challenges for the accurate assessment of the impact of novel therapies on viral growth and decay. Using the example of influenza A, we illustrate how the measurement of infection-related quantities that determine the dynamics of viral load within the human...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930163/ https://www.ncbi.nlm.nih.gov/pubmed/27367230 http://dx.doi.org/10.1371/journal.pone.0158237 |
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author | Vegvari, Carolin Hadjichrysanthou, Christoforos Cauët, Emilie Lawrence, Emma Cori, Anne de Wolf, Frank Anderson, Roy M. |
author_facet | Vegvari, Carolin Hadjichrysanthou, Christoforos Cauët, Emilie Lawrence, Emma Cori, Anne de Wolf, Frank Anderson, Roy M. |
author_sort | Vegvari, Carolin |
collection | PubMed |
description | Acute viral infections pose many practical challenges for the accurate assessment of the impact of novel therapies on viral growth and decay. Using the example of influenza A, we illustrate how the measurement of infection-related quantities that determine the dynamics of viral load within the human host, can inform investigators on the course and severity of infection and the efficacy of a novel treatment. We estimated the values of key infection-related quantities that determine the course of natural infection from viral load data, using Markov Chain Monte Carlo methods. The data were placebo group viral load measurements collected during volunteer challenge studies, conducted by Roche, as part of the oseltamivir trials. We calculated the values of the quantities for each patient and the correlations between the quantities, symptom severity and body temperature. The greatest variation among individuals occurred in the viral load peak and area under the viral load curve. Total symptom severity correlated positively with the basic reproductive number. The most sensitive endpoint for therapeutic trials with the goal to cure patients is the duration of infection. We suggest laboratory experiments to obtain more precise estimates of virological quantities that can supplement clinical endpoint measurements. |
format | Online Article Text |
id | pubmed-4930163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49301632016-07-18 How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? Vegvari, Carolin Hadjichrysanthou, Christoforos Cauët, Emilie Lawrence, Emma Cori, Anne de Wolf, Frank Anderson, Roy M. PLoS One Research Article Acute viral infections pose many practical challenges for the accurate assessment of the impact of novel therapies on viral growth and decay. Using the example of influenza A, we illustrate how the measurement of infection-related quantities that determine the dynamics of viral load within the human host, can inform investigators on the course and severity of infection and the efficacy of a novel treatment. We estimated the values of key infection-related quantities that determine the course of natural infection from viral load data, using Markov Chain Monte Carlo methods. The data were placebo group viral load measurements collected during volunteer challenge studies, conducted by Roche, as part of the oseltamivir trials. We calculated the values of the quantities for each patient and the correlations between the quantities, symptom severity and body temperature. The greatest variation among individuals occurred in the viral load peak and area under the viral load curve. Total symptom severity correlated positively with the basic reproductive number. The most sensitive endpoint for therapeutic trials with the goal to cure patients is the duration of infection. We suggest laboratory experiments to obtain more precise estimates of virological quantities that can supplement clinical endpoint measurements. Public Library of Science 2016-07-01 /pmc/articles/PMC4930163/ /pubmed/27367230 http://dx.doi.org/10.1371/journal.pone.0158237 Text en © 2016 Vegvari et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Vegvari, Carolin Hadjichrysanthou, Christoforos Cauët, Emilie Lawrence, Emma Cori, Anne de Wolf, Frank Anderson, Roy M. How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title | How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title_full | How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title_fullStr | How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title_full_unstemmed | How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title_short | How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections? |
title_sort | how can viral dynamics models inform endpoint measures in clinical trials of therapies for acute viral infections? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930163/ https://www.ncbi.nlm.nih.gov/pubmed/27367230 http://dx.doi.org/10.1371/journal.pone.0158237 |
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