Analyses of asthma severity phenotypes and inflammatory proteins in subjects stratified by sputum granulocytes

被引:358
作者
Hastie, Annette T. [1 ]
Moore, Wendy C. [1 ]
Meyers, Deborah A. [1 ]
Vestal, Penny L. [1 ]
Li, Huashi [1 ]
Peters, Stephen P. [1 ]
Bleecker, Eugene R. [1 ]
机构
[1] Wake Forest Univ Hlth Sci, Ctr Human Genom, Winston Salem, NC 27157 USA
关键词
Asthma phenotypes; protein microarrays; BDNF; CXCL13; TNFSF14; CCL20; CCL18; EPIDERMAL-GROWTH-FACTOR; EOSINOPHILIC AIRWAY INFLAMMATION; BRONCHIAL EPITHELIAL-CELLS; NECROSIS-FACTOR-ALPHA; BECLOMETHASONE DIPROPIONATE; NEUTROPHILIC INFLAMMATION; NEUROTROPHIC FACTOR; PERSISTENT ASTHMA; CLUSTER-ANALYSIS; RESEARCH-PROGRAM;
D O I
10.1016/j.jaci.2010.02.008
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Patients with severe asthma have increased granulocytes in their sputum compared with patients with mild to moderate asthma. Objective: We hypothesized that inflammatory granulocytes in sputum may identify specific asthma severity phenotypes and are associated with different patterns of inflammatory proteins in sputum supernatants. Methods: This hypothesis was tested in 242 patients with asthma enrolled in the Severe Asthma Research Program who provided sputum samples for cell count, differential cell determinations, cell lysates for Western blot, and supernatant analyses by inflammatory protein microarrays and ELISAs. ANOVA and multiple linear regression models tested mediator associations. Results: Stratified by sputum granulocytes, <2% or >= 2% eosinophils and <40% or >= 40% neutrophils, subjects with both increased eosinophils and neutrophils had the lowest lung function and increased symptoms and health care use. Subjects with elevated eosinophils with or without increased neutrophils had significantly increased fraction exhaled nitric oxide (FeNO) and serum eosinophils and greater frequency of daily beta-agonist use. Microarray data stratified by granulocytes revealed 25 to 28 inflammatory proteins increased >2-fold in sputa with >= 40% neutrophils. Microarray analyses stratified by severity of asthma identified 6 to 9 proteins increased >2-fold in sputa in subjects with severe asthma compared with nonsevere asthma. ELISA data stratified by sputum granulocytes showed significant increases in brain-derived neurotrophic factor, IL-1 beta, and macrophage inflammatory protein 3 alpha/CCL20 for those with >= 40% neutrophils; these mediators demonstrated positive associations with neutrophil counts. Conclusion: Combined increased sputum eosinophils and neutrophils identified patients with asthma with the lowest lung function, worse asthma control, and increased symptoms and health care requirements. Inflammatory protein analyses of sputum supernatants found novel mediators increased in patients with asthma, predominantly associated with increased sputum neutrophils. (J Allergy Clin Immunol 2010;125:1028-36.)
引用
收藏
页码:1028 / 1036
页数:9
相关论文
共 53 条
  • [1] The ENFUMOSA cross-sectional European multicentre study of the clinical phenotype of chronic severe asthma
    Abraham, B
    Antó, JM
    Barreiro, E
    Bel, EHD
    Bonsignore, G
    Bousquet, J
    Castellsague, J
    Chanez, P
    Cibella, F
    Cuttitta, G
    Dahlén, B
    Dahlén, SE
    Drews, N
    Djukanovic, R
    Fabbri, LM
    Folkerts, G
    Gaga, M
    Gratziou, C
    Guerrera, G
    Holgate, ST
    Howarth, PH
    Johnston, SL
    Kanniess, F
    Kips, JC
    Kerstjens, HAM
    Kumlin, M
    Magnussen, H
    Nijkamp, FP
    Papageorgiou, N
    Papi, A
    Postma, DS
    Pauwels, RA
    Rabe, KF
    Richter, K
    Roldaan, AC
    Romagnoli, M
    Roquet, A
    Sanjuas, C
    Siafakas, NM
    Timens, W
    Tzanakis, N
    Vachier, I
    Vignola, AM
    Watson, L
    Yourgioti, G
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (03) : 470 - 477
  • [2] American Thoracic Society, 2000, AM J RESP CRIT CARE, V162, P2341
  • [3] Expression of epidermal growth factor and epidermal growth factor receptor immunoreactivity in the asthmatic human airway
    Amishima, M
    Munakata, M
    Nasuhara, Y
    Sato, A
    Takahashi, T
    Homma, Y
    Kawakami, Y
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (06) : 1907 - 1912
  • [4] IL-1, IL-18, and IL-33 families of cytokines
    Arend, William P.
    Palmer, Gaby
    Gabay, Cem
    [J]. IMMUNOLOGICAL REVIEWS, 2008, 223 : 20 - 38
  • [5] Imbalance between vascular endothelial growth factor and endostatin levels in induced sputum from asthmatic subjects
    Asai, K
    Kanazawa, H
    Otani, K
    Shiraishi, S
    Hirata, K
    Yoshikawa, J
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (04) : 571 - 575
  • [6] Clinical assessment of asthma severity partially corresponds to sputum eosirophilic airway inflammation
    Bartoli, ML
    Bacci, E
    Carnevali, S
    Cianchetti, S
    Dente, FL
    Di Franco, A
    Giannini, D
    Taccola, M
    Vagaggini, B
    Paggiaro, PL
    [J]. RESPIRATORY MEDICINE, 2004, 98 (02) : 184 - 193
  • [7] The use of exhaled nitric oxide concentration to identify eosinophilic airway inflammation: an observational study in adults with asthma
    Berry, MA
    Shaw, DE
    Green, RH
    Brightling, CE
    Wardlaw, AJ
    Pavord, ID
    [J]. CLINICAL AND EXPERIMENTAL ALLERGY, 2005, 35 (09) : 1175 - 1179
  • [8] Pathological features and inhaled corticosteroid response of eosinophilic and non-eosinophilic asthma
    Berry, Mike
    Morgan, Angela
    Shaw, Dominick E.
    Parker, Deborah
    Green, Ruth
    Brightling, Christopher
    Bradding, Peter
    Wardlaw, Andrew J.
    Pavord, Ian D.
    [J]. THORAX, 2007, 62 (12) : 1043 - 1049
  • [9] Cellular sources of enhanced brain-derived neurotrophic factor production in a mouse model of allergic inflammation
    Braun, A
    Lommatzsch, M
    Mannsfeldt, A
    Neuhaus-Steinmetz, U
    Fischer, A
    Schnoy, N
    Lewin, GR
    Renz, H
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 21 (04) : 537 - 546
  • [10] Monocyte-like and mature macrophages produce CXCL13 (B cell-attracting chemokine 1) in inflammatory lesions with lymphoid neogenesis
    Carlsen, HS
    Baekkevold, ES
    Morton, HC
    Haraldsen, G
    Brandtzaeg, P
    [J]. BLOOD, 2004, 104 (10) : 3021 - 3027