IMMUNOHISTOCHEMICAL DISTRIBUTION AND SERUM LEVELS OF THE CA2+-BINDING PROTEINS MRP8, MRP14 AND THEIR HETERODIMERIC FORM MRP8/14 IN CROHNS-DISEASE

被引:98
作者
LUGERING, N
STOLL, R
KUCHARZIK, T
SCHMID, KW
ROHLMANN, G
BURMEISTER, G
SORG, C
DOMSCHKE, W
机构
[1] UNIV MUNSTER,DEPT PATHOL,D-48129 MUNSTER,GERMANY
[2] UNIV MUNSTER,INST EXPTL DERMATOL,D-48129 MUNSTER,GERMANY
[3] BMA BIOMED AG,AUGST,SWITZERLAND
关键词
CALCIUM-BINDING PROTEINS; MRP8; MRP; 14; 27E10; CROHNS DISEASE; IMMUNOHISTOCHEMISTRY; IMMUNOASSAY;
D O I
10.1159/000201267
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In previous histochemical studies the distribution of the two Ca2+-binding proteins MRP8 and MRP14 as well as their heterocomplex MRP8/14 has been demonstrated in different inflammatory diseases. Monoclonal antibodies against MRP8 and MRP14 and their heterodimer MRP8/14 (27E10 epitope) were used to investigate immunohistochemically the distribution of these proteins in routinely processed small and large bowel tissues from patients with Crohn's disease (CD). Furthermore, we used a sandwich immunoassay to measure serum concentrations of MRPs in 62 patients with CD and in 20 healthy controls. Disease activities of CD patients were simultaneously assessed by the Crohn's disease activity index (CDAI) and the severity activity index of Goebell (SAI). In our immunohistochemical study, MRP8, MRP 14 and the heterocomplex MRP8/14 were demonstrated in the majority of granulocytes and macrophages in active CD. Additionally, a strong complex MRP8/14 immunoreactivity was present in epithelial cells adjacent to ulcerative and fissuring lesions in the bowel. Serum MRP8/14 concentrations were significantly (p < 0.0001) increased in patients with active CD (CDAI > 150, SAI > 120). No correlations were found for level of MRP 14 and MRP8 alone, respectively. The follow-up of individual patients with initially active CD showed a further increase in MRP8/14 levels during acute attacks of the inflammatory process. We suggest that our assay for MRP8/14 discriminates well between active and inactive CD and may have considerable potential in the analysis of clinical disease activity in CD patients. Our morphological results confirm the finding of increased MRP8/14 serum levels in patients with active CD.
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页码:406 / 414
页数:9
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