CORRELATION OF EOSINOPHILS, EOSINOPHIL CATIONIC PROTEIN AND SOLUBLE INTERLEUKIN-2 RECEPTOR WITH THE CLINICAL ACTIVITY OF ATOPIC-DERMATITIS

被引:129
作者
KAGI, MK
JOLLERJEMELKA, H
WUTHRICH, B
机构
[1] UNIV HOSP ZURICH, DEPT DERMATOL, ALLERGY UNIT, CH-8091 ZURICH, SWITZERLAND
[2] UNIV HOSP ZURICH, DEPT INTERNAL MED, CLIN IMMUNOL SECT, CH-8091 ZURICH, SWITZERLAND
关键词
ATOPIC DERMATITIS; CLINICAL ACTIVITY; EOSINOPHILS; SOLUBLE INTERLEUKIN-2 RECEPTOR; EOSINOPHIL CATIONIC PROTEIN; SOLUBLE CD23; LACTATE DEHYDROGENASE;
D O I
10.1159/000247419
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
To evaluate the correlation with the clinical activity of atopic dermatitis (AD) we investigated prospectively cellular and serological parameters such as eosinophils, eosinophil cationic protein (ECP), soluble IL-2 receptor (sIL-2R), soluble CD23 (sCD23) and lactate dehydrogenase (LDH) in peripheral blood of 37 AD patients on admission to and discharge from the Department of Dermatology at the University Hospital in Zurich. On admission the actual clinical skin condition as measured by the skin intensity score (SIS) was significantly correlated with eosinophils (p<0.005), ECP (p<0.05) and sIL-2R (p<0.001). During the observation period a significant improvement in the clinical status as measured by the SIS was observed in all AD patients (p<0.001). A significant decrease in sIL-2R (p<0.005), which was most pronounced in the group of AD patients receiving systemic steroids, together with a decrease in eosinophils and ECP but not in sCD23 and LDH could be demonstrated between admission and discharge. In addition., a slight but significant increase in peripheral blood lymphocytes (p<0.005) and monocytes (p<0.01) was noted. Comparing the 'extrinsic' (n=32) and the 'intrinsic' (n=5) types of AD no significant differences with regard to the above mentioned parameters were found. Our data indicate that cellular and serological parameters such as eosinophils, ECP and sIL-2R reflect the clinical activity of AD and may therefore give further insights into the pathogenesis of this disease.
引用
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页码:88 / 92
页数:5
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