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Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells

The relatively new technology of DNA microarrays offers the possibility to probe the human genome for clues to the pathogenesis and treatment of human disease. While early studies using this approach were largely in oncology, many new reports are emerging in other fields including infectious disease...

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Detalles Bibliográficos
Autores principales: Olsen, Nancy J, Moore, Jason H, Aune, Thomas M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC416456/
https://www.ncbi.nlm.nih.gov/pubmed/15142262
http://dx.doi.org/10.1186/ar1190
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author Olsen, Nancy J
Moore, Jason H
Aune, Thomas M
author_facet Olsen, Nancy J
Moore, Jason H
Aune, Thomas M
author_sort Olsen, Nancy J
collection PubMed
description The relatively new technology of DNA microarrays offers the possibility to probe the human genome for clues to the pathogenesis and treatment of human disease. While early studies using this approach were largely in oncology, many new reports are emerging in other fields including infectious diseases and pharmacology, and applications in autoimmunity have been recently reported by our group and others. Some of these investigations have examined animal models of autoimmune disease, but a number of human studies have also been carried out. Of special interest are those that have used peripheral blood samples because, unlike tissue biopsies, these are readily available from all subjects. Using this approach, patterns of gene expression can be detected that distinguish patients with autoimmune conditions from normal subjects. Furthermore, the genes that are identified provide clues to possible pathogenetic mechanisms and are likely to be useful in developing tests to establish diagnostic categories and predict therapeutic responses.
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spelling pubmed-4164562004-05-22 Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells Olsen, Nancy J Moore, Jason H Aune, Thomas M Arthritis Res Ther Review The relatively new technology of DNA microarrays offers the possibility to probe the human genome for clues to the pathogenesis and treatment of human disease. While early studies using this approach were largely in oncology, many new reports are emerging in other fields including infectious diseases and pharmacology, and applications in autoimmunity have been recently reported by our group and others. Some of these investigations have examined animal models of autoimmune disease, but a number of human studies have also been carried out. Of special interest are those that have used peripheral blood samples because, unlike tissue biopsies, these are readily available from all subjects. Using this approach, patterns of gene expression can be detected that distinguish patients with autoimmune conditions from normal subjects. Furthermore, the genes that are identified provide clues to possible pathogenetic mechanisms and are likely to be useful in developing tests to establish diagnostic categories and predict therapeutic responses. BioMed Central 2004 2004-04-29 /pmc/articles/PMC416456/ /pubmed/15142262 http://dx.doi.org/10.1186/ar1190 Text en Copyright © 2004 BioMed Central Ltd
spellingShingle Review
Olsen, Nancy J
Moore, Jason H
Aune, Thomas M
Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title_full Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title_fullStr Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title_full_unstemmed Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title_short Gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
title_sort gene expression signatures for autoimmune disease in peripheral blood mononuclear cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC416456/
https://www.ncbi.nlm.nih.gov/pubmed/15142262
http://dx.doi.org/10.1186/ar1190
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