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

被引:48
作者
Bjornsdottir, Unnur S. [1 ]
Holgate, Stephen T. [2 ]
Reddy, Padmalatha S. [3 ]
Hill, Andrew A. [3 ]
McKee, Charlotte M. [4 ]
Csimma, Cristina I. [4 ]
Weaver, Amy A. [3 ]
Legault, Holly M. [4 ]
Small, Clayton G. [4 ]
Ramsey, Renee C. [3 ]
Ellis, Debra K. [4 ]
Burke, Conor M. [5 ]
Thompson, Philip J. [6 ,7 ]
Howarth, Peter H. [2 ]
Wardlaw, Andrew J. [8 ]
Bardin, Phillip G. [9 ,10 ]
Bernstein, David I. [11 ]
Irving, Louis B. [12 ]
Chupp, Geoffrey L. [13 ]
Bensch, George W. [14 ]
Bensch, Gregory W. [14 ]
Stahlman, Jon E. [15 ]
Karetzky, Monroe [16 ]
Baker, James W. [17 ]
Miller, Rachel L. [18 ]
Goodman, Brad H. [19 ]
Raible, Donald G. [3 ]
Goldman, Samuel J. [3 ]
Miller, Douglas K. [3 ]
Ryan, John L. [4 ]
Dorner, Andrew J. [4 ]
Immermann, Frederick W. [3 ]
O'Toole, Margot [3 ]
机构
[1] Univ Iceland, Dept Allergy Clin Immunol, Reykjavik, Iceland
[2] Univ Southampton, Southampton, Hants, England
[3] Pfizer, Cambridge, MA USA
[4] Wyeth Res, Cambridge, MA USA
[5] James Connolly Mem Hosp, Dublin, Ireland
[6] Univ Western Australia, Lung Inst WA, Crawley, Australia
[7] Univ Western Australia, Ctr Asthma Allergy & Resp Res, Crawley, Australia
[8] Univ Leicester, Leicester, Leics, England
[9] Monash Univ, Melbourne, Vic 3004, Australia
[10] Med Ctr, Melbourne, Vic, Australia
[11] Univ Cincinnati, Coll Med, Cincinnati, OH USA
[12] Royal Melbourne Hosp, Parkville, Vic 3050, Australia
[13] Yale Univ, Sch Med, New Haven, CT USA
[14] Bensch Clin Res, Stockton, CA USA
[15] Ctr Asthma & Allergy, Conyers, GA USA
[16] Newark Beth Israel Med Ctr, Newark, NJ USA
[17] Baker Allergy Asthma & Dermatol, Lake Oswego, OR USA
[18] Columbia Univ, Med Ctr, New York, NY USA
[19] Coastal Allergy & Asthma, Savannah, GA USA
来源
PLOS ONE | 2011年 / 6卷 / 07期
关键词
REGULATORY FACTOR-1 POLYMORPHISMS; TOLL-LIKE RECEPTORS; INNATE IMMUNITY; ATOPIC ASTHMA; CD14; GENE; T-CELLS; B-CELL; ASSOCIATION; PROTEIN; IL-15;
D O I
10.1371/journal.pone.0021902
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:19
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