IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay
<p>Abstract</p> <p>Background</p> <p>IFN-γ responses to <it>M. tuberculosis </it>antigens are used as <it>in-vitro </it>diagnostic tests for tuberculosis infection. The tests are highly specific but sensitivity may be impaired due to immuno-suppr...
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doaj-ff606c11a5bf44458354eed1d8a17e542020-11-25T01:34:29ZengBMCBMC Research Notes1756-05002009-02-01211910.1186/1756-0500-2-19IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assayRabna PauloBjerregaard-Andersen MortenRuhwald MortenEugen-Olsen JesperRavn Pernille<p>Abstract</p> <p>Background</p> <p>IFN-γ responses to <it>M. tuberculosis </it>antigens are used as <it>in-vitro </it>diagnostic tests for tuberculosis infection. The tests are highly specific but sensitivity may be impaired due to immuno-suppression. The objective of this small exploratory study was to compare three novel biomarkers for <it>in-vitro </it>diagnosis of tuberculosis – MCP-1, MCP-3 and IL-1RA – with the current established biomarker IFN-γ and the newly described IP-10 and MCP-2.</p> <p>Methods</p> <p>Whole blood from 8 patents with active tuberculosis and from 7 healthy controls was stimulated with <it>M. tuberculosis </it>specific antigens and mitogen in the Quantiferon In Tube test tubes. Levels of biomarkers were measured using Luminex and ELISA (IFN-γ).</p> <p>Results</p> <p>We found all five new biomarkers were expressed in significantly higher concentrations compared to IFN-γ. IP-10 and MCP-3 levels in the un-stimulated samples were higher in patients compared with controls.</p> <p>Conclusion</p> <p>All biomarkers had diagnostic potential as they could differentiate between the patients and the controls. IP-10 and MCP-2 seemed most promising as they were expressed in high levels with antigen stimulation and were low in the un-stimulated samples. Further studies are needed to explore the potential of these highly expressed novel biomarkers individually and in combination.</p> http://www.biomedcentral.com/1756-0500/2/19 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rabna Paulo Bjerregaard-Andersen Morten Ruhwald Morten Eugen-Olsen Jesper Ravn Pernille |
spellingShingle |
Rabna Paulo Bjerregaard-Andersen Morten Ruhwald Morten Eugen-Olsen Jesper Ravn Pernille IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay BMC Research Notes |
author_facet |
Rabna Paulo Bjerregaard-Andersen Morten Ruhwald Morten Eugen-Olsen Jesper Ravn Pernille |
author_sort |
Rabna Paulo |
title |
IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay |
title_short |
IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay |
title_full |
IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay |
title_fullStr |
IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay |
title_full_unstemmed |
IP-10, MCP-1, MCP-2, MCP-3, and IL-1RA hold promise as biomarkers for infection with <it>M. tuberculosis </it>in a whole blood based T-cell assay |
title_sort |
ip-10, mcp-1, mcp-2, mcp-3, and il-1ra hold promise as biomarkers for infection with <it>m. tuberculosis </it>in a whole blood based t-cell assay |
publisher |
BMC |
series |
BMC Research Notes |
issn |
1756-0500 |
publishDate |
2009-02-01 |
description |
<p>Abstract</p> <p>Background</p> <p>IFN-γ responses to <it>M. tuberculosis </it>antigens are used as <it>in-vitro </it>diagnostic tests for tuberculosis infection. The tests are highly specific but sensitivity may be impaired due to immuno-suppression. The objective of this small exploratory study was to compare three novel biomarkers for <it>in-vitro </it>diagnosis of tuberculosis – MCP-1, MCP-3 and IL-1RA – with the current established biomarker IFN-γ and the newly described IP-10 and MCP-2.</p> <p>Methods</p> <p>Whole blood from 8 patents with active tuberculosis and from 7 healthy controls was stimulated with <it>M. tuberculosis </it>specific antigens and mitogen in the Quantiferon In Tube test tubes. Levels of biomarkers were measured using Luminex and ELISA (IFN-γ).</p> <p>Results</p> <p>We found all five new biomarkers were expressed in significantly higher concentrations compared to IFN-γ. IP-10 and MCP-3 levels in the un-stimulated samples were higher in patients compared with controls.</p> <p>Conclusion</p> <p>All biomarkers had diagnostic potential as they could differentiate between the patients and the controls. IP-10 and MCP-2 seemed most promising as they were expressed in high levels with antigen stimulation and were low in the un-stimulated samples. Further studies are needed to explore the potential of these highly expressed novel biomarkers individually and in combination.</p> |
url |
http://www.biomedcentral.com/1756-0500/2/19 |
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