Plasma RANTES and eotaxin levels are correlated with the severity of chronic rhinosinusitis

被引:19
作者
Chao, Pin-Zhir [1 ,2 ]
Chou, Chi-Ming [3 ]
Chen, Chen-Ho [4 ]
机构
[1] Taipei Med Univ, Shuang Ho Hosp, Dept Otolaryngol, New Taipei, Taiwan
[2] Taipei Med Univ, Grad Inst Clin Med, Taipei, Taiwan
[3] Taipei Med Univ, Grad Inst Med Sci, Taipei, Taiwan
[4] Taipei Med Univ, Sch Med Lab Sci & Biotechnol, Taipei, Taiwan
关键词
RANTES; Eotaxin; Nasal polyps; Chronic rhinosinusitis; Eosinophils; CHRONIC HYPERPLASTIC SINUSITIS; NASAL POLYPS; EOSINOPHIL INFILTRATION; MESSENGER-RNA; FIBROBLASTS; DIAGNOSIS; MUCOSA; CELLS;
D O I
10.1007/s00405-012-1927-5
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Eosinophilia occurs in up to 75-90% of nasal polyps in Caucasians. The chemokines eotaxin and RANTES increase eosinophil recruitment, activation, and survival, and these chemokines are significantly expressed in nasal polyps. We hypothesized that eotaxin and RANTES plasma levels might be correlated with disease severity. We compared the eotaxin and RANTES plasma levels in 20 Taiwanese patients with chronic rhinosinusitis and nasal polyps and 20 Taiwanese healthy controls. Eotaxin and RANTES plasma levels were measured by ELISA and disease severity was scored by CT scans. Compared to controls, patients with nasal polyps had significantly elevated plasma levels of eotaxin and RANTES and increased peripheral blood eosinophils (p < 0.001). Eotaxin plasma levels were significantly correlated with disease severity in patients with chronic rhinosinusitis to a greater extent than were RANTES levels. RANTES and eotaxin levels were also positively correlated with the percentages of peripheral blood eosinophils. Eotaxin plasma levels are significantly correlated with disease severity in Taiwanese patients with nasal polyposis to a greater degree than are RANTES levels. Additional studies are needed to assess whether eotaxin plasma levels can be used to monitor disease progression and attenuation.
引用
收藏
页码:2343 / 2348
页数:6
相关论文
共 28 条
[1]   Characterization of the eosinophil chemokine RANTES in nasal polyps [J].
Allen, JS ;
Eisma, R ;
Leonard, G ;
LaFreniere, D ;
Kreutzer, D .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1998, 107 (05) :416-420
[2]  
Bartels Joachim, 1997, Rhinology (Utrecht), V35, P171
[3]   Adult chronic rhinosinusitis: Definitions, diagnosis, epidemiology, and pathophysiology [J].
Benninger, MS .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2003, 129 (03) :S1-S32
[4]   The molecular biology of nasal polyposis [J].
Bernstein J.M. .
Current Allergy and Asthma Reports, 2001, 1 (3) :262-267
[5]   A superantigen hypothesis for the pathogenesis of chronic hyperplastic sinusitis with massive nasal polyposis [J].
Bernstein, JM ;
Ballow, M ;
Schlievert, PM ;
Rich, G ;
Allen, C ;
Dryja, D .
AMERICAN JOURNAL OF RHINOLOGY, 2003, 17 (06) :321-326
[6]   An update on the classifications, diagnosis, and treatment of rhinosinusitis [J].
Chan, Yvonne ;
Kuhn, Frederick A. .
CURRENT OPINION IN OTOLARYNGOLOGY & HEAD AND NECK SURGERY, 2009, 17 (03) :204-208
[7]  
Couto Luciano Gustavo Ferreira, 2008, Braz J Otorhinolaryngol, V74, P207
[8]   Interleukin 5, IL6, IL12, IFN-γ, RANTES and Fractalkine in human nasal polyps, turbinate mucosa and serum [J].
Danielsen, Arild ;
Tynning, Turid ;
Brokstad, Karl A. ;
Olofsson, Jan ;
Davidsson, Ake .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2006, 263 (03) :282-289
[9]   Measurement of inflammatory mediators of mast cells and eosinophils in native nasal lavage fluid in nasal polyposis [J].
Di Lorenzo, G ;
Drago, A ;
Pellitteri, ME ;
Candore, G ;
Colombo, A ;
Gervasi, F ;
Pacor, ML ;
D'Ambrosio, FP ;
Caruso, C .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 125 (02) :164-175
[10]   Eosinophil infiltration and activation in nasal polyposis [J].
Fan, Guo-Kang ;
Wang, Hualin ;
Takenaka, Hiroshi .
ACTA OTO-LARYNGOLOGICA, 2007, 127 (05) :521-526