Transcriptomics in Human Challenge Models

Human challenge models, in which volunteers are experimentally infected with a pathogen of interest, provide the opportunity to directly identify both natural and vaccine-induced correlates of protection. In this review, we highlight how the application of transcriptomics to human challenge studies...

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Main Authors: Amber J. Barton, Jennifer Hill, Andrew J. Pollard, Christoph J. Blohmke
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.01839/full
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author Amber J. Barton
Jennifer Hill
Andrew J. Pollard
Christoph J. Blohmke
author_facet Amber J. Barton
Jennifer Hill
Andrew J. Pollard
Christoph J. Blohmke
author_sort Amber J. Barton
collection DOAJ
description Human challenge models, in which volunteers are experimentally infected with a pathogen of interest, provide the opportunity to directly identify both natural and vaccine-induced correlates of protection. In this review, we highlight how the application of transcriptomics to human challenge studies allows for the identification of novel correlates and gives insight into the immunological pathways required to develop functional immunity. In malaria challenge trials for example, innate immune pathways appear to play a previously underappreciated role in conferring protective immunity. Transcriptomic analyses of samples obtained in human challenge studies can also deepen our understanding of the immune responses preceding symptom onset, allowing characterization of innate immunity and early gene signatures, which may influence disease outcome. Influenza challenge studies demonstrate that these gene signatures have diagnostic potential in the context of pandemics, in which presymptomatic diagnosis of at-risk individuals could allow early initiation of antiviral treatment and help limit transmission. Furthermore, gene expression analysis facilitates the identification of host factors contributing to disease susceptibility, such as C4BPA expression in enterotoxigenic Escherichia coli infection. Overall, these studies highlight the exceptional value of transcriptional data generated in human challenge trials and illustrate the broad impact molecular data analysis may have on global health through rational vaccine design and biomarker discovery.
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spelling doaj.art-7a899e1e225d46ff83f0724d050051222022-12-21T17:45:39ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-12-01810.3389/fimmu.2017.01839317950Transcriptomics in Human Challenge ModelsAmber J. Barton0Jennifer Hill1Andrew J. Pollard2Christoph J. Blohmke3Oxford Vaccine Group, Department of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, United KingdomOxford Vaccine Group, Department of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, United KingdomOxford Vaccine Group, Department of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, United KingdomOxford Vaccine Group, Department of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Centre, Oxford, United KingdomHuman challenge models, in which volunteers are experimentally infected with a pathogen of interest, provide the opportunity to directly identify both natural and vaccine-induced correlates of protection. In this review, we highlight how the application of transcriptomics to human challenge studies allows for the identification of novel correlates and gives insight into the immunological pathways required to develop functional immunity. In malaria challenge trials for example, innate immune pathways appear to play a previously underappreciated role in conferring protective immunity. Transcriptomic analyses of samples obtained in human challenge studies can also deepen our understanding of the immune responses preceding symptom onset, allowing characterization of innate immunity and early gene signatures, which may influence disease outcome. Influenza challenge studies demonstrate that these gene signatures have diagnostic potential in the context of pandemics, in which presymptomatic diagnosis of at-risk individuals could allow early initiation of antiviral treatment and help limit transmission. Furthermore, gene expression analysis facilitates the identification of host factors contributing to disease susceptibility, such as C4BPA expression in enterotoxigenic Escherichia coli infection. Overall, these studies highlight the exceptional value of transcriptional data generated in human challenge trials and illustrate the broad impact molecular data analysis may have on global health through rational vaccine design and biomarker discovery.http://journal.frontiersin.org/article/10.3389/fimmu.2017.01839/fulltranscriptomicsvaccinesfunctional genomicsbiomarkersmicroarrayhuman challenge
spellingShingle Amber J. Barton
Jennifer Hill
Andrew J. Pollard
Christoph J. Blohmke
Transcriptomics in Human Challenge Models
Frontiers in Immunology
transcriptomics
vaccines
functional genomics
biomarkers
microarray
human challenge
title Transcriptomics in Human Challenge Models
title_full Transcriptomics in Human Challenge Models
title_fullStr Transcriptomics in Human Challenge Models
title_full_unstemmed Transcriptomics in Human Challenge Models
title_short Transcriptomics in Human Challenge Models
title_sort transcriptomics in human challenge models
topic transcriptomics
vaccines
functional genomics
biomarkers
microarray
human challenge
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.01839/full
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AT jenniferhill transcriptomicsinhumanchallengemodels
AT andrewjpollard transcriptomicsinhumanchallengemodels
AT christophjblohmke transcriptomicsinhumanchallengemodels