Lügering N, Stoll R, Schmid K W, Kucharzik T, Stein H, Burmeister G, Sorg C, Domschke W
Department of Medicine B, University of Münster, Germany.
Eur J Clin Invest. 1995 Sep;25(9):659-64. doi: 10.1111/j.1365-2362.1995.tb01982.x.
MRP8, MRP14 and their heterodimer MRP8/14 (27E10 antigen) are myeloic related proteins which have been shown to have a major role in inflammatory and immunological responses. In the present study monospecific antibodies against MRPs were used to investigate immunohistochemically the distribution of these proteins in routinely processed bowel tissues from 23 patients with ulcerative colitis (UC). MRP8, MRP14 and their heterocomplex MRP8/14 were demonstrated in the majority of granulocytes and macrophages in tissues of patients with active UC. Furthermore by employing the ELISA technique we measured MRP8/14 serum levels in 62 patients with UC and the results were compared with those for healthy controls. Disease activities were determined by established clinical activity indices. Serum MRP8/14 concentrations were significantly (P < 0.0001) increased in patients with active ulcerative colitis. No enhancement of serum levels were found for MRP14 and MRP8 alone, respectively. The follow-up of individual patients with initially active disease showed a decrease of MRP8/14 serum levels in parallel with clinical improvement following the start of therapy. It is thus concluded that MRP8/14 accurately reflects the degree of disease activity in UC. Further, possible biological function of MRPs seems to be associated with the heterodimeric form (27E10 antigen) rather than with individual proteins. Our morphological results confirm the finding of enhanced MRP8/14 serum levels in patients with active UC.
MRP8、MRP14及其异源二聚体MRP8/14(27E10抗原)是髓系相关蛋白,已被证明在炎症和免疫反应中起主要作用。在本研究中,使用针对MRP的单特异性抗体,通过免疫组织化学方法研究了这些蛋白在23例溃疡性结肠炎(UC)患者常规处理的肠道组织中的分布。在活动期UC患者的组织中,大多数粒细胞和巨噬细胞中都检测到了MRP8、MRP14及其异源复合物MRP8/14。此外,我们采用酶联免疫吸附测定(ELISA)技术检测了62例UC患者的MRP8/14血清水平,并将结果与健康对照者进行了比较。疾病活动度通过既定的临床活动指数来确定。活动期溃疡性结肠炎患者的血清MRP8/14浓度显著升高(P<0.0001)。单独检测MRP14和MRP8时,未发现血清水平升高。对最初患有活动期疾病的个体患者进行随访发现,开始治疗后,随着临床症状改善,MRP8/14血清水平下降。因此得出结论,MRP8/14能准确反映UC的疾病活动程度。此外,MRP的可能生物学功能似乎与异源二聚体形式(27E10抗原)有关,而非与单个蛋白有关。我们的形态学结果证实了活动期UC患者血清中MRP8/14水平升高这一发现。