Th1 and Th2 cell population in chronic ethmoidal rhinosinusitis: A chemokine receptor assay

被引:25
作者
Elhini, A
Abdelwahab, S
Ikeda, K
机构
[1] Juntendo Univ, Sch Med, Dept Otorhinolaryngol, Bunkyo Ku, Tokyo 1138421, Japan
[2] Tohoku Univ, Grad Sch Med Sci, Div Histol, Dept Cell Biol, Sendai, Miyagi, Japan
关键词
D O I
10.1097/01.MLG.0000165380.64445.EE
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Background: It is necessary for the immune system in the nasal and paranasal sinus mucosa to possess appropriate responses to infective agents as well as allergic responses. Recently, the T helper (Th)1/Th2 paradigm has been proposed as a new concept to explain various immunologic phenomena. Objective. Toward the goal of better understanding chronic rhino-sinusitis, we have tried to define the predominating helper T-cell subsets among patients with chronic rhino-sinusitis through characterizing the expressed chemokine receptors by these cells to find out the relation between these chemokine receptors' expression and the underlying pathogenesis of chronic rhinosinusitis. Methods: Thirty patients with ethmoidal chronic rhinosinusitis were used in our study. Patients were divided into atopic and nonatopic groups according to their serum immunoglobulin (Ig)E levels. Samples from ethmoidal sinus mucosa were processed as follows: frozen sections were examined immunohistochemically for detection of CCR4, CCR5, and EG2 positive cells and the mRNA of CCR4, and CCR5 transcripts were then examined by real-time quantitative polymerase chain reaction (PCR). Results: By immunohistochemistry, atopic patients showed high expression of CCR4 and EG2 positive cells, whereas nonatopic patients showed high expression of CCR5 positive cells. The expression of CCR4 and CCR5 mRNA, detected by real-time quantitative PCR supported the data obtained by immunohistochemistry. Conclusion: The present study suggests that eosinophil recruitment associated with Th2 cell infiltration is the main factor responsible for the pathology of atopic rhinosinusitis.
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页码:1272 / 1277
页数:6
相关论文
共 15 条
[1]
Campbell J. Darren, 2000, Archivum Immunologiae et Therapiae Experimentalis, V48, P451
[2]
Molecular pathology of allergic disease - II: Upper airway disease [J].
Christodoulopoulos, P ;
Cameron, L ;
Durham, S ;
Hamid, Q .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (02) :211-223
[3]
Glimcher LH, 2000, GENE DEV, V14, P1693
[4]
The one-two of T helper cells: Does interferon-gamma knock out the Th2 hypothesis for asthma? [J].
Holtzman, MJ ;
Sampath, D ;
Castro, M ;
Look, DC ;
Jayaraman, S .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (04) :316-318
[5]
Chronic sinusitis: Risk factors for extensive disease [J].
Hoover, GE ;
Newman, LJ ;
PlattsMills, TAE ;
Phillips, CD ;
Gross, CW ;
Wheatley, LM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 100 (02) :185-191
[6]
Subjective and objective evaluation in endoscopic sinus surgery [J].
Ikeda, K ;
Kondo, Y ;
Sunose, H ;
Hirano, K ;
Oshima, T ;
Shimomura, A ;
Suzuki, H ;
Takasaka, T .
AMERICAN JOURNAL OF RHINOLOGY, 1996, 10 (04) :217-220
[7]
Jankowski R, 2002, RHINOLOGY, V40, P173
[8]
Molecular immunology and immunotherapy for chronic sinusitis [J].
Nguyen, LHP ;
Fakhri, S ;
Frenkiel, S ;
Hamid, QA .
CURRENT ALLERGY AND ASTHMA REPORTS, 2003, 3 (06) :505-512
[9]
Impact of rhinitis on airway inflammation: biological and therapeutic implications [J].
Passalacqua, G ;
Canonica, GW .
RESPIRATORY RESEARCH, 2001, 2 (06) :320-323
[10]
Cytokines and chemoattractants in allergic inflammation [J].
Romagnani, S .
MOLECULAR IMMUNOLOGY, 2002, 38 (12-13) :881-885