Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vegvari, Carolin, Hadjichrysanthou, Christoforos, Cauët, Emilie, Lawrence, Emma, Cori, Anne, de Wolf, Frank, Anderson, Roy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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
_version_ 1782440704294780928
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
work_keys_str_mv AT vegvaricarolin howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT hadjichrysanthouchristoforos howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT cauetemilie howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT lawrenceemma howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT corianne howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT dewolffrank howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections
AT andersonroym howcanviraldynamicsmodelsinformendpointmeasuresinclinicaltrialsoftherapiesforacuteviralinfections