Innate responses to Aspergillus:: Role of C1q and pentraxin 3 in nasal polyposis

被引:6
作者
Baruah, Paramita
Trimarchi, Matteo
Dumitriu, Ingrid E.
Dell'Antonio, Giacomo
Doglioni, Claudio
Rovere-Querini, Patrizia
Bussi, Mario
Manfredi, Angelo A.
机构
[1] H San Raffaele Sci Inst, Canc Immunotherapy & Gene Therapy Program, Clin Immunol Unit, I-20132 Milan, Italy
[2] H San Raffaele, Dept Otorhinolaryngol, Milan, Italy
[3] H San Raffaele, Dept Pathol, Milan, Italy
[4] Univ Vita Salute San Raffaele, Milan, Italy
来源
AMERICAN JOURNAL OF RHINOLOGY | 2007年 / 21卷 / 02期
关键词
Aspergillus; C1q; inflammation; innate immunity; nasal polyp etiology; nasal polyposis; PTX3;
D O I
10.2500/ajr.2007.21.2980
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: Pentraxin 3 (PTX3) and complement component C1q are humoral factors of innate immunity, produced at sites of inflammation, and are essential in immune defense against several microbes such as Aspergillus, which is commonly implicated in nasal polyposis. Methods: PTX3 and C1q were measured in nasal polyp tissue, normal nasal mucosa, and serum of patients and healthy subjects. Immunohistochemistry for the two proteins was done on normal nasal mucosa and nasal polyps. In addition, PTX3 and C1q production from mononuclear cells from patients and healthy subjects was assessed. Results: Normal nasal mucosa was found to have 100-fold higher levels of PTX3 compared with serum. No measurable local increase of PTX3 was observed in polyps compared with normal mucosa. Immunohistochemistry revealed PTX3 expression in the lining of blood vessels both within normal mucosa and nasal polyps. PTX3 also was present in mononuclear cells infiltrating nasal polyps. C1q levels were higher in polyps than in normal nasal mucosa. Conclusion: High levels of PTX3 arc present in normal nasal mucosa, suggesting a role in the maintenance of tissue homeostasis. Elevated C1q levels in nasal polyps might be indicative of an ongoing inflammatory response in the nasal mucosa in these patients.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 33 条
[1]   Pulmonary dendritic cells producing IL-10 mediate tolerance induced by respiratory exposure to antigen [J].
Akbari, O ;
DeKruyff, RH ;
Umetsu, DT .
NATURE IMMUNOLOGY, 2001, 2 (08) :725-731
[2]   ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR CLQ IN HUMAN-SERUM BY USE OF MONOCLONAL-ANTIBODIES [J].
ANTES, U ;
HEINZ, HP ;
LOOS, M .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 74 (02) :299-306
[3]  
BARUAH P, 2005, BLOOD, V15, P15
[4]   The tissue pentraxin PTX3 limits C1q-mediated complement activation and phagocytosis of apoptotic cells by dendritic cells [J].
Baruah, Paramita ;
Dumitriu, Ingrid E. ;
Peri, Giuseppe ;
Russo, Vincenzo ;
Mantovani, Alberto ;
Manfredi, Angelo A. ;
Rovere-Querini, Patrizia .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 80 (01) :87-95
[5]   Lymphocyte subpopulations and cytokines in nasal polyps: Is there a local immune system in the nasal polyp? [J].
Bernstein, JM ;
Ballow, M ;
Rich, G ;
Allen, C ;
Swanson, M ;
Dmochowski, J .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2004, 130 (05) :526-535
[6]  
Bernstein Joel M, 2005, Curr Opin Otolaryngol Head Neck Surg, V13, P39, DOI 10.1097/00020840-200502000-00010
[7]   C1q, autoimmunity and apoptosis [J].
Botto, M ;
Walport, MJ .
IMMUNOBIOLOGY, 2002, 205 (4-5) :395-406
[8]   Maturation of dendritic cells abrogates C1q production in vivo and in vitro [J].
Castellano, G ;
Woltman, AM ;
Nauta, AJ ;
Roos, A ;
Trouw, LA ;
Seelen, MA ;
Schena, FP ;
Daha, MR ;
van Kooten, C .
BLOOD, 2004, 103 (10) :3813-3820
[9]   Expression of human β-defensin 2 in human nasal mucosa [J].
Chen, PH ;
Fang, SY .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2004, 261 (05) :238-241
[10]   Chronic sinusitis with nasal polyps: Staphylococcal exotoxin immunoglobulin E and cellular inflammation [J].
Conley, DB ;
Tripathi, A ;
Ditto, AM ;
Reid, K ;
Grammer, LC ;
Kern, RC .
AMERICAN JOURNAL OF RHINOLOGY, 2004, 18 (05) :273-278