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Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM)
BACKGROUND: Rapid detection and therapeutic intervention for infectious and emerging diseases is a major scientific goal in biodefense and public health. Toward this end, cytokine profiles in human blood were investigated using a human whole blood ex vivo exposure model, called WEEM. RESULTS: Sample...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430575/ https://www.ncbi.nlm.nih.gov/pubmed/22607329 http://dx.doi.org/10.1186/1471-2180-12-79 |
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author | Chromy, Brett A Fodor, Imola K Montgomery, Nancy K Luciw, Paul A McCutchen-Maloney, Sandra L |
author_facet | Chromy, Brett A Fodor, Imola K Montgomery, Nancy K Luciw, Paul A McCutchen-Maloney, Sandra L |
author_sort | Chromy, Brett A |
collection | PubMed |
description | BACKGROUND: Rapid detection and therapeutic intervention for infectious and emerging diseases is a major scientific goal in biodefense and public health. Toward this end, cytokine profiles in human blood were investigated using a human whole blood ex vivo exposure model, called WEEM. RESULTS: Samples of whole blood from healthy volunteers were incubated with seven pathogens including Yersinia pseudotuberculosis, Yersinia enterocolitica, Bacillus anthracis, and multiple strains of Yersinia pestis, and multiplexed protein expression profiling was conducted on supernatants of these cultures with an antibody array to detect 30 cytokines simultaneously. Levels of 8 cytokines, IL-1α, IL-1β, IL-6, IL-8, IL-10, IP-10, MCP-1 and TNFα, were significantly up-regulated in plasma after bacterial exposures of 4 hours. Statistical clustering was applied to group the pathogens based on the host response protein expression profiles. The nearest phylogenetic neighbors clustered more closely than the more distant pathogens, and all seven pathogens were clearly differentiated from the unexposed control. In addition, the Y. pestis and Yersinia near neighbors were differentiated from the B. anthracis strains. CONCLUSIONS: Cluster analysis, based on host response cytokine profiles, indicates that distinct patterns of immunomodulatory proteins are induced by the different pathogen exposures and these patterns may enable further development into biomarkers for diagnosing pathogen exposure. |
format | Online Article Text |
id | pubmed-3430575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34305752012-08-30 Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) Chromy, Brett A Fodor, Imola K Montgomery, Nancy K Luciw, Paul A McCutchen-Maloney, Sandra L BMC Microbiol Research Article BACKGROUND: Rapid detection and therapeutic intervention for infectious and emerging diseases is a major scientific goal in biodefense and public health. Toward this end, cytokine profiles in human blood were investigated using a human whole blood ex vivo exposure model, called WEEM. RESULTS: Samples of whole blood from healthy volunteers were incubated with seven pathogens including Yersinia pseudotuberculosis, Yersinia enterocolitica, Bacillus anthracis, and multiple strains of Yersinia pestis, and multiplexed protein expression profiling was conducted on supernatants of these cultures with an antibody array to detect 30 cytokines simultaneously. Levels of 8 cytokines, IL-1α, IL-1β, IL-6, IL-8, IL-10, IP-10, MCP-1 and TNFα, were significantly up-regulated in plasma after bacterial exposures of 4 hours. Statistical clustering was applied to group the pathogens based on the host response protein expression profiles. The nearest phylogenetic neighbors clustered more closely than the more distant pathogens, and all seven pathogens were clearly differentiated from the unexposed control. In addition, the Y. pestis and Yersinia near neighbors were differentiated from the B. anthracis strains. CONCLUSIONS: Cluster analysis, based on host response cytokine profiles, indicates that distinct patterns of immunomodulatory proteins are induced by the different pathogen exposures and these patterns may enable further development into biomarkers for diagnosing pathogen exposure. BioMed Central 2012-05-20 /pmc/articles/PMC3430575/ /pubmed/22607329 http://dx.doi.org/10.1186/1471-2180-12-79 Text en Copyright ©2012 Chromy et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chromy, Brett A Fodor, Imola K Montgomery, Nancy K Luciw, Paul A McCutchen-Maloney, Sandra L Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title | Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title_full | Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title_fullStr | Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title_full_unstemmed | Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title_short | Cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (WEEM) |
title_sort | cluster analysis of host cytokine responses to biodefense pathogens in a whole blood ex vivo exposure model (weem) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430575/ https://www.ncbi.nlm.nih.gov/pubmed/22607329 http://dx.doi.org/10.1186/1471-2180-12-79 |
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