Pollen-derived adenosine is a necessary cofactor for ragweed allergy

被引:31
作者
Wimmer, M. [1 ,2 ,3 ,4 ]
Alessandrini, F. [2 ,3 ,4 ]
Gilles, S. [1 ,4 ]
Frank, U. [4 ,5 ]
Oeder, S. [2 ,3 ,4 ]
Hauser, M. [4 ,6 ]
Ring, J. [4 ,7 ]
Ferreira, F. [6 ]
Ernst, D. [5 ]
Winkler, J. B. [8 ]
Schmitt-Kopplin, P. [9 ,10 ]
Ohnmacht, C. [2 ,3 ]
Behrendt, H. [2 ,3 ,4 ]
Schmidt-Weber, C. [2 ,3 ]
Traidl-Hoffmann, C. [1 ,4 ,7 ]
Gutermuth, J. [2 ,3 ,7 ,11 ]
机构
[1] Tech Univ Munich, UNIKA T, Inst Environm Med, D-80290 Munich, Germany
[2] Tech Univ Munich, Ctr Allergy & Environm ZAUM, D-80290 Munich, Germany
[3] Helmholtz Zentrum Munchen, Munich, Germany
[4] Christine Kuhne Ctr Allergy Res & Educ, Zurich, Switzerland
[5] Helmholtz Zentrum Munchen, Inst Biochem Plant Pathol, Munich, Germany
[6] Salzburg Univ, Dept Mol Biol, Christian Doppler Lab Allergy Diag & Therapy, A-5020 Salzburg, Austria
[7] Tech Univ Munich, Dept Dermatol & Allergy Biederstein, Munich, Germany
[8] Helmholtz Zentrum Munchen, Inst Biochem Plant Pathol, Res Unit Environm Simulat, Munich, Germany
[9] Helmholtz Zentrum Munchen, Res Unit Analyt BioGeoChem, Munich, Germany
[10] Tech Univ Munich, Analyt Food Chem, D-80290 Munich, Germany
[11] Vrije Univ Brussel, Univ Ziekenhuis Brussel, Dept Dermatol, Brussels, Belgium
关键词
adenosine; adjuvant; allergic inflammation; ragweed; sensitization; AIRWAY INFLAMMATION; LUNG INFLAMMATION; IMMUNE-RESPONSES; MOUSE MODEL; PULMONARY INFLAMMATION; LIPID MEDIATORS; V; RECEPTOR; ASTHMA; MICE;
D O I
10.1111/all.12642
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BackgroundRagweed (Ambrosia artemisiifolia) is a strong elicitor of allergic airway inflammation with worldwide increasing prevalence. Various components of ragweed pollen are thought to play a role in the development of allergic responses. The aim of this study was to identify critical factors for allergenicity of ragweed pollen in a physiological model of allergic airway inflammation. MethodsAqueous ragweed pollen extract, the low molecular weight fraction or the major allergen Amb a 1 was instilled intranasally on 1-11 consecutive days, and allergic airway inflammation was evaluated by bronchoalveolar lavage, lung histology, serology, gene expression in lung tissue, and measurement of lung function. Pollen-derived adenosine was removed from the extract enzymatically to analyze its role in ragweed-induced allergy. Migration of human neutrophils and eosinophils toward supernatants of ragweed-stimulated bronchial epithelial cells was analyzed. ResultsInstillation of ragweed pollen extract, but not of the major allergen or the low molecular weight fraction, induced specific IgG(1), pulmonary infiltration with inflammatory cells, a Th2-associated cytokine signature in pulmonary tissue, and impaired lung function. Adenosine aggravated ragweed-induced allergic lung inflammation. In vitro, human neutrophils and eosinophils migrated toward supernatants of bronchial epithelial cells stimulated with ragweed extract only if adenosine was present. ConclusionsPollen-derived adenosine is a critical factor in ragweed-pollen-induced allergic airway inflammation. Future studies aim at therapeutic strategies to control these allergen-independent pathways.
引用
收藏
页码:944 / 954
页数:11
相关论文
共 40 条
[1]   Effects of ultrafine carbon particle inhalation on allergic inflammation of the lung [J].
Alessandrini, F ;
Schulz, H ;
Takenaka, S ;
Lentner, B ;
Karg, E ;
Behrendt, H ;
Jakob, T .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (04) :824-830
[2]   Effects of ultrafine particles-induced oxidative stress on Clara cells in allergic lung inflammation [J].
Alessandrini, Francesca ;
Weichenmeier, Ingrid ;
van Miert, Erik ;
Takenaka, Shinji ;
Karg, Erwin ;
Blume, Cornelia ;
Mempel, Martin ;
Schulz, Holger ;
Bernard, Alfred ;
Behrendt, Heidrun .
PARTICLE AND FIBRE TOXICOLOGY, 2010, 7
[3]   Hyperresponsiveness to adenosine in sensitized Wistar rats over-expressing A1 receptor [J].
Alfieri, Alessio ;
Parisi, Antonio ;
Maione, Francesco ;
Grassia, Gianluca ;
Morello, Silvana ;
Ialenti, Armando ;
Mascolo, Nicola ;
Cicala, Carla .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2012, 695 (1-3) :120-125
[4]   Immunity, inflammation and cancer: a leading role for adenosine [J].
Antonioli, Luca ;
Blandizzi, Corrado ;
Pacher, Pal ;
Hasko, Gyoergy .
NATURE REVIEWS CANCER, 2013, 13 (12) :842-857
[5]   Innate IL-13-producing nuocytes arise during allergic lung inflammation and contribute to airways hyperreactivity [J].
Barlow, Jillian L. ;
Bellosi, Agustin ;
Hardman, Clare S. ;
Drynan, Lesley F. ;
Wong, See Heng ;
Cruickshank, James P. ;
McKenzie, Andrew N. J. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (01) :191-U275
[6]   Role of Arginase 1 from Myeloid Cells in Th2-Dominated Lung Inflammation [J].
Barron, Luke ;
Smith, Amber M. ;
El Kasmi, Karim C. ;
Qualls, Joseph E. ;
Huang, Xiaozhu ;
Cheever, Allen ;
Borthwick, Lee A. ;
Wilson, Mark S. ;
Murray, Peter J. ;
Wynn, Thomas A. .
PLOS ONE, 2013, 8 (04)
[7]   High Environmental Ozone Levels Lead to Enhanced Allergenicity of Birch Pollen [J].
Beck, Isabelle ;
Jochner, Susanne ;
Gilles, Stefanie ;
McIntyre, Mareike ;
Buters, Jeroen T. M. ;
Schmidt-Weber, Carsten ;
Behrendt, Heidrun ;
Ring, Johannes ;
Menzel, Annette ;
Traidl-Hoffmann, Claudia .
PLOS ONE, 2013, 8 (11)
[8]   Secretion of proinflammatory eicosanoid-like substances precedes allergen release from pollen grains in the initiation of allergic sensitization [J].
Behrendt, H ;
Kasche, A ;
von Eschenbach, CE ;
Risse, U ;
Huss-Marp, J ;
Ring, J .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 124 (1-3) :121-125
[9]   Metabolic consequences of adenosine deaminase deficiency in mice are associated with defects in alveogenesis, pulmonary inflammation, and airway obstruction [J].
Blackburn, MR ;
Volmer, JB ;
Thrasher, JL ;
Zhong, HY ;
Crosby, JR ;
Lee, JJ ;
Kellems, RE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :159-170
[10]   The allergen Bet v 1 in fractions of ambient air deviates from birch pollen counts [J].
Buters, J. T. M. ;
Weichenmeier, I. ;
Ochs, S. ;
Pusch, G. ;
Kreyling, W. ;
Boere, A. J. F. ;
Schober, W. ;
Behrendt, H. .
ALLERGY, 2010, 65 (07) :850-858