Intravenous anti-IL-5 monoclonal antibody reduces eosinophils and tenascin deposition in allergen-challenged human atopic skin

被引:74
作者
Phipps, S [1 ]
Flood-Page, P [1 ]
Menzies-Gow, A [1 ]
Ong, YE [1 ]
Kay, AB [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, NHLI Div, Dept Allergy & Clin Immunol, London SW3 6LY, England
基金
英国惠康基金;
关键词
anti-IL-5; eosinophil; late-phase reaction; skin; tenascin;
D O I
10.1111/j.0022-202X.2004.22619.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Anti-IL-5 monoclonal antibody (mepolizumab) reduces baseline bronchial mucosal eosinophils and deposition of extracellular matrix proteins in the reticular basement membrane in mild asthma. Here we report the effect of anti-IL-5, in the same patients, on allergen-induced eosinophil accumulation, tenascin deposition (as a marker of repair and remodelling) and the magnitude of the late-phase allergic cutaneous reaction. Skin biopsies were performed in 24 atopic subjects at allergen- and diluent-injected sites before 6 and 48 h after, three infusions of a humanized, monoclonal antibody against IL-5 (mepolizumab) using a randomized double-blind, placebo-controlled design. Anti-IL-5 significantly inhibited eosinophil infiltration in 6 h and 48 h skin biopsies as well as the numbers of tenascin immunoreactive cells at 48 h. In contrast, anti-IL-5 had no significant effect on the size of the 6 or 48 h late-phase cutaneous allergic reaction. This study (a) suggests that eosinophils are unlikely to cause the redness, swelling, and induration characteristic of the peak (6 h) late-phase cutaneous allergic reaction and (b) shows that decreases in tenascin positive cells at 48 h correlates with reduction of eosinophils, so providing further evidence of involvement in remodelling processes associated with allergic inflammation.
引用
收藏
页码:1406 / 1412
页数:7
相关论文
共 34 条
[1]   LOCALIZATION OF EOSINOPHIL GRANULE MAJOR BASIC-PROTEIN IN HUMAN BASOPHILS [J].
ACKERMAN, SJ ;
KEPHART, GM ;
HABERMANN, TM ;
GREIPP, PR ;
GLEICH, GJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (03) :946-961
[2]   Mice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response [J].
Ashcroft, GS ;
Yang, X ;
Glick, AB ;
Weinstein, M ;
Letterio, JJ ;
Mizel, DE ;
Anzano, M ;
Greenwell-Wild, T ;
Wahl, SM ;
Deng, CX ;
Roberts, AB .
NATURE CELL BIOLOGY, 1999, 1 (05) :260-266
[3]   IDENTIFICATION OF ACTIVATED LYMPHOCYTES-T AND EOSINOPHILS IN BRONCHIAL BIOPSIES IN STABLE ATOPIC ASTHMA [J].
AZZAWI, M ;
BRADLEY, B ;
JEFFERY, PK ;
FREW, AJ ;
WARDLAW, AJ ;
KNOWLES, G ;
ASSOUFI, B ;
COLLINS, JV ;
DURHAM, S ;
KAY, AB .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 142 (06) :1407-1413
[4]   Airway subepithelial fibrosis in a murine model of atopic asthma - Suppression by dexamethasone or anti-interleukin-5 antibody [J].
Blyth, DI ;
Wharton, TF ;
Pedrick, MS ;
Savage, TJ ;
Sanjar, S .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 23 (02) :241-246
[5]  
Church M. K., 1997, ALLERGY ALLERGIC DIS, P149
[6]  
DENBURG JA, 1991, BLOOD, V77, P1462
[7]   TENASCIN - AN EXTRACELLULAR-MATRIX PROTEIN PROMINENT IN SPECIALIZED EMBRYONIC-TISSUES AND TUMORS [J].
ERICKSON, HP ;
BOURDON, MA .
ANNUAL REVIEW OF CELL BIOLOGY, 1989, 5 :71-92
[8]   Anti-IL-5 treatment reduces deposition of ECM proteins in the bronchial subepithelial basement membrane of mild atopic asthmatics [J].
Flood-Page, P ;
Menzies-Gow, A ;
Phipps, S ;
Ying, S ;
Wangoo, A ;
Ludwig, MS ;
Barnes, N ;
Robinson, D ;
Kay, AB .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (07) :1029-1036
[9]   Eosinophil's role remains uncertain as anti-interleukin-5 only partially depletes numbers in asthmatic airway [J].
Flood-Page, PT ;
Menzies-Gow, AN ;
Kay, AB ;
Robinson, DS .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (02) :199-204
[10]  
FREW AJ, 1988, J IMMUNOL, V141, P4158