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Microarray analysis of gene expression in lupus

Recent advances in the study of global patterns of gene expression with the use of microarray technology, coupled with data analysis using sophisticated statistical algorithms, have provided new insights into pathogenic mechanisms of disease. Complementary and reproducible data from multiple laborat...

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Detalles Bibliográficos
Autores principales: Crow, Mary K, Wohlgemuth, Jay
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC333417/
https://www.ncbi.nlm.nih.gov/pubmed/14680503
http://dx.doi.org/10.1186/ar1015
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author Crow, Mary K
Wohlgemuth, Jay
author_facet Crow, Mary K
Wohlgemuth, Jay
author_sort Crow, Mary K
collection PubMed
description Recent advances in the study of global patterns of gene expression with the use of microarray technology, coupled with data analysis using sophisticated statistical algorithms, have provided new insights into pathogenic mechanisms of disease. Complementary and reproducible data from multiple laboratories have documented the feasibility of analysis of heterogeneous populations of peripheral blood mononuclear cells from patients with rheumatic diseases through use of this powerful technology. Although some patterns of gene expression, including increased expression of immune system cell surface activation molecules, confirm previous data obtained with other techniques, some novel genes that are differentially expressed have been identified. Most interesting is the dominant pattern of interferon-induced gene expression detected among blood mononuclear cells from patients with systemic lupus erythematosus and juvenile dermatomyositis. These data are consistent with longstanding observations indicating increased circulating interferon-α in the blood of patients with active lupus, but draw attention to the dominance of the interferon pathway in the hierarchy of gene expression pathways implicated in systemic autoimmunity.
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spelling pubmed-3334172004-02-07 Microarray analysis of gene expression in lupus Crow, Mary K Wohlgemuth, Jay Arthritis Res Ther Review Recent advances in the study of global patterns of gene expression with the use of microarray technology, coupled with data analysis using sophisticated statistical algorithms, have provided new insights into pathogenic mechanisms of disease. Complementary and reproducible data from multiple laboratories have documented the feasibility of analysis of heterogeneous populations of peripheral blood mononuclear cells from patients with rheumatic diseases through use of this powerful technology. Although some patterns of gene expression, including increased expression of immune system cell surface activation molecules, confirm previous data obtained with other techniques, some novel genes that are differentially expressed have been identified. Most interesting is the dominant pattern of interferon-induced gene expression detected among blood mononuclear cells from patients with systemic lupus erythematosus and juvenile dermatomyositis. These data are consistent with longstanding observations indicating increased circulating interferon-α in the blood of patients with active lupus, but draw attention to the dominance of the interferon pathway in the hierarchy of gene expression pathways implicated in systemic autoimmunity. BioMed Central 2003 2003-10-13 /pmc/articles/PMC333417/ /pubmed/14680503 http://dx.doi.org/10.1186/ar1015 Text en Copyright © 2003 BioMed Central Ltd
spellingShingle Review
Crow, Mary K
Wohlgemuth, Jay
Microarray analysis of gene expression in lupus
title Microarray analysis of gene expression in lupus
title_full Microarray analysis of gene expression in lupus
title_fullStr Microarray analysis of gene expression in lupus
title_full_unstemmed Microarray analysis of gene expression in lupus
title_short Microarray analysis of gene expression in lupus
title_sort microarray analysis of gene expression in lupus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC333417/
https://www.ncbi.nlm.nih.gov/pubmed/14680503
http://dx.doi.org/10.1186/ar1015
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