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Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood

BACKGROUND: Asthma exacerbations remain a major unmet clinical need. The difficulty in obtaining airway tissue and bronchoalveolar lavage samples during exacerbations has greatly hampered study of naturally occurring exacerbations. This study was conducted to determine if mRNA profiling of periphera...

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Autores principales: Bjornsdottir, Unnur S., Holgate, Stephen T., Reddy, Padmalatha S., Hill, Andrew A., McKee, Charlotte M., Csimma, Cristina I., Weaver, Amy A., Legault, Holly M., Small, Clayton G., Ramsey, Renee C., Ellis, Debra K., Burke, Conor M., Thompson, Philip J., Howarth, Peter H., Wardlaw, Andrew J., Bardin, Phillip G., Bernstein, David I., Irving, Louis B., Chupp, Geoffrey L., Bensch, George W., Bensch, Gregory W., Stahlman, Jon E., Karetzky, Monroe, Baker, James W., Miller, Rachel L., Goodman, Brad H., Raible, Donald G., Goldman, Samuel J., Miller, Douglas K., Ryan, John L., Dorner, Andrew J., Immermann, Frederick W., O'Toole, Margot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136489/
https://www.ncbi.nlm.nih.gov/pubmed/21779351
http://dx.doi.org/10.1371/journal.pone.0021902
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author Bjornsdottir, Unnur S.
Holgate, Stephen T.
Reddy, Padmalatha S.
Hill, Andrew A.
McKee, Charlotte M.
Csimma, Cristina I.
Weaver, Amy A.
Legault, Holly M.
Small, Clayton G.
Ramsey, Renee C.
Ellis, Debra K.
Burke, Conor M.
Thompson, Philip J.
Howarth, Peter H.
Wardlaw, Andrew J.
Bardin, Phillip G.
Bernstein, David I.
Irving, Louis B.
Chupp, Geoffrey L.
Bensch, George W.
Bensch, Gregory W.
Stahlman, Jon E.
Karetzky, Monroe
Baker, James W.
Miller, Rachel L.
Goodman, Brad H.
Raible, Donald G.
Goldman, Samuel J.
Miller, Douglas K.
Ryan, John L.
Dorner, Andrew J.
Immermann, Frederick W.
O'Toole, Margot
author_facet Bjornsdottir, Unnur S.
Holgate, Stephen T.
Reddy, Padmalatha S.
Hill, Andrew A.
McKee, Charlotte M.
Csimma, Cristina I.
Weaver, Amy A.
Legault, Holly M.
Small, Clayton G.
Ramsey, Renee C.
Ellis, Debra K.
Burke, Conor M.
Thompson, Philip J.
Howarth, Peter H.
Wardlaw, Andrew J.
Bardin, Phillip G.
Bernstein, David I.
Irving, Louis B.
Chupp, Geoffrey L.
Bensch, George W.
Bensch, Gregory W.
Stahlman, Jon E.
Karetzky, Monroe
Baker, James W.
Miller, Rachel L.
Goodman, Brad H.
Raible, Donald G.
Goldman, Samuel J.
Miller, Douglas K.
Ryan, John L.
Dorner, Andrew J.
Immermann, Frederick W.
O'Toole, Margot
author_sort Bjornsdottir, Unnur S.
collection PubMed
description BACKGROUND: Asthma exacerbations remain a major unmet clinical need. The difficulty in obtaining airway tissue and bronchoalveolar lavage samples during exacerbations has greatly hampered study of naturally occurring exacerbations. This study was conducted to determine if mRNA profiling of peripheral blood mononuclear cells (PBMCs) could provide information on the systemic molecular pathways involved during asthma exacerbations. METHODOLOGY/PRINCIPAL FINDINGS: Over the course of one year, gene expression levels during stable asthma, exacerbation, and two weeks after an exacerbation were compared using oligonucleotide arrays. For each of 118 subjects who experienced at least one asthma exacerbation, the gene expression patterns in a sample of peripheral blood mononuclear cells collected during an exacerbation episode were compared to patterns observed in multiple samples from the same subject collected during quiescent asthma. Analysis of covariance identified genes whose levels of expression changed during exacerbations and returned to quiescent levels by two weeks. Heterogeneity among visits in expression profiles was examined using K-means clustering. Three distinct exacerbation-associated gene expression signatures were identified. One signature indicated that, even among patients without symptoms of respiratory infection, genes of innate immunity were activated. Antigen-independent T cell activation mediated by IL15 was also indicated by this signature. A second signature revealed strong evidence of lymphocyte activation through antigen receptors and subsequent downstream events of adaptive immunity. The number of genes identified in the third signature was too few to draw conclusions on the mechanisms driving those exacerbations. CONCLUSIONS/SIGNIFICANCE: This study has shown that analysis of PBMCs reveals systemic changes accompanying asthma exacerbation and has laid the foundation for future comparative studies using PBMCs.
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spelling pubmed-31364892011-07-21 Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood Bjornsdottir, Unnur S. Holgate, Stephen T. Reddy, Padmalatha S. Hill, Andrew A. McKee, Charlotte M. Csimma, Cristina I. Weaver, Amy A. Legault, Holly M. Small, Clayton G. Ramsey, Renee C. Ellis, Debra K. Burke, Conor M. Thompson, Philip J. Howarth, Peter H. Wardlaw, Andrew J. Bardin, Phillip G. Bernstein, David I. Irving, Louis B. Chupp, Geoffrey L. Bensch, George W. Bensch, Gregory W. Stahlman, Jon E. Karetzky, Monroe Baker, James W. Miller, Rachel L. Goodman, Brad H. Raible, Donald G. Goldman, Samuel J. Miller, Douglas K. Ryan, John L. Dorner, Andrew J. Immermann, Frederick W. O'Toole, Margot PLoS One Research Article BACKGROUND: Asthma exacerbations remain a major unmet clinical need. The difficulty in obtaining airway tissue and bronchoalveolar lavage samples during exacerbations has greatly hampered study of naturally occurring exacerbations. This study was conducted to determine if mRNA profiling of peripheral blood mononuclear cells (PBMCs) could provide information on the systemic molecular pathways involved during asthma exacerbations. METHODOLOGY/PRINCIPAL FINDINGS: Over the course of one year, gene expression levels during stable asthma, exacerbation, and two weeks after an exacerbation were compared using oligonucleotide arrays. For each of 118 subjects who experienced at least one asthma exacerbation, the gene expression patterns in a sample of peripheral blood mononuclear cells collected during an exacerbation episode were compared to patterns observed in multiple samples from the same subject collected during quiescent asthma. Analysis of covariance identified genes whose levels of expression changed during exacerbations and returned to quiescent levels by two weeks. Heterogeneity among visits in expression profiles was examined using K-means clustering. Three distinct exacerbation-associated gene expression signatures were identified. One signature indicated that, even among patients without symptoms of respiratory infection, genes of innate immunity were activated. Antigen-independent T cell activation mediated by IL15 was also indicated by this signature. A second signature revealed strong evidence of lymphocyte activation through antigen receptors and subsequent downstream events of adaptive immunity. The number of genes identified in the third signature was too few to draw conclusions on the mechanisms driving those exacerbations. CONCLUSIONS/SIGNIFICANCE: This study has shown that analysis of PBMCs reveals systemic changes accompanying asthma exacerbation and has laid the foundation for future comparative studies using PBMCs. Public Library of Science 2011-07-14 /pmc/articles/PMC3136489/ /pubmed/21779351 http://dx.doi.org/10.1371/journal.pone.0021902 Text en Bjornsdottir et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bjornsdottir, Unnur S.
Holgate, Stephen T.
Reddy, Padmalatha S.
Hill, Andrew A.
McKee, Charlotte M.
Csimma, Cristina I.
Weaver, Amy A.
Legault, Holly M.
Small, Clayton G.
Ramsey, Renee C.
Ellis, Debra K.
Burke, Conor M.
Thompson, Philip J.
Howarth, Peter H.
Wardlaw, Andrew J.
Bardin, Phillip G.
Bernstein, David I.
Irving, Louis B.
Chupp, Geoffrey L.
Bensch, George W.
Bensch, Gregory W.
Stahlman, Jon E.
Karetzky, Monroe
Baker, James W.
Miller, Rachel L.
Goodman, Brad H.
Raible, Donald G.
Goldman, Samuel J.
Miller, Douglas K.
Ryan, John L.
Dorner, Andrew J.
Immermann, Frederick W.
O'Toole, Margot
Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title_full Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title_fullStr Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title_full_unstemmed Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title_short Pathways Activated during Human Asthma Exacerbation as Revealed by Gene Expression Patterns in Blood
title_sort pathways activated during human asthma exacerbation as revealed by gene expression patterns in blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136489/
https://www.ncbi.nlm.nih.gov/pubmed/21779351
http://dx.doi.org/10.1371/journal.pone.0021902
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