EVIDENCE OF INTERCELLULAR-ADHESION MOLECULE-1 EXPRESSION ON NASAL EPITHELIAL-CELLS IN ACUTE RHINOCONJUNCTIVITIS CAUSED BY POLLEN EXPOSURE

被引:67
作者
CIPRANDI, G [1 ]
PRONZATO, C [1 ]
RICCA, V [1 ]
BAGNASCO, M [1 ]
CANONICA, GW [1 ]
机构
[1] UNIV GENOA,DIMI,DEPT INTERNAL MED,ALLERGY & CLIN IMMUNOL SERV,I-16132 GENOA,ITALY
关键词
RHINOCONJUNCTIVITIS; POLLEN ALLERGY; ADHESION MOLECULES; CD54; EPITHELIAL CELLS; INFLAMMATORY CELLS;
D O I
10.1016/0091-6749(94)90182-1
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Rhinoconjunctivitis caused by pollen allergy is characterized by typical signs and symptoms and mucosal infiltration by inflammatory cells during pollen season. It has been recently demonstrated that the adhesion molecule system is deeply involved in cell-to-cell interaction during inflammatory response consequent to allergic reactions. The aim of this study was to evaluate the expression of intercellular adhesion molecule-1 (ICAM-1 or CD54) on nasal epithelial cells, before and during natural seasonal exposure, in 10 allergic patients (Parietaria judaica-sensitized) and in 10 healthy volunteers, correlating this parameter with clinical and cytologic involvement. Nasal epithelial cells of allergic subjects showed a significant expression of CD54 during pollen season (p < 0.001). On the contrary, no CD54 expression was observed out of pollen season. In healthy volunteers no CD54 expression was observed both before and during pollen season. Cytologic evaluation demonstrated an infiltration by eosinophils (mainly activated [EG2+]), (p < 0.001), neutrophils (p < 0.001), and metachromatic cells (p < 0.001) during pollen season only in allergic subjects. Therefore results indicate that seasonal allergic rhinitis is characterized by an infiltration of inflammatory cells correlated with CD54 expression on nasal epithelial cells. This phenomenon is specific, being restricted only to allergic patients during pollen season.
引用
收藏
页码:738 / 746
页数:9
相关论文
共 39 条
[1]  
ADAMS DH, 1989, LANCET, V2, P1122
[2]  
BAGNASCO M, 1993, SEP EUR AC ALL CLIN
[3]   KERATINOCYTES AS INITIATORS OF INFLAMMATION [J].
BARKER, JNWN ;
MITRA, RS ;
GRIFFITHS, CEM ;
DIXIT, VM ;
NICKOLOFF, BJ .
LANCET, 1991, 337 (8735) :211-214
[4]  
Barnes P J, 1991, Clin Exp Allergy, V21 Suppl 1, P80, DOI 10.1111/j.1365-2222.1991.tb01710.x
[5]   IMMUNOHISTOLOGY OF THE NASAL-MUCOSA IN SEASONAL ALLERGIC RHINITIS - INCREASES IN ACTIVATED EOSINOPHILS AND EPITHELIAL MAST-CELLS [J].
BENTLEY, AM ;
JACOBSON, MR ;
CUMBERWORTH, V ;
BARKANS, JR ;
MOQBEL, R ;
SCHWARTZ, LB ;
IRANI, AMA ;
KAY, AB ;
DURHAM, SR .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (04) :877-883
[6]   T-CELL ADHESION MOLECULES [J].
BIERER, BE ;
BURAKOFF, SJ .
FASEB JOURNAL, 1988, 2 (10) :2584-2590
[7]  
BONINI S, 1990, J ALLERGY CLIN IMMUN, V886, P69
[8]   EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039
[9]   PROINFLAMMATORY CYTOKINES IN ACUTE ASTHMA [J].
BROWN, PH ;
CROMPTON, GK ;
GREENING, AP .
LANCET, 1991, 338 (8767) :590-593
[10]  
CANONICA GW, 1991, ALLERGY CLIN IMMUN S, V1, P28