Adsorptive Depletion of Elevated Proinflammatory CD14+CD16+DR++Monocytes in Patients With Inflammatory Bowel Disease

CD14型 CD16 促炎细胞因子 医学 单核细胞 炎症性肠病 免疫学 溃疡性结肠炎 内科学 流式细胞术 炎症 抗原 CD3型 疾病 CD8型
作者
Hiroyuki Hanai,Takayuki Iida,Ken Takeuchi,Fumio Watanabe,Masami Yamada,Masataka Kikuyama,Yasushi Maruyama,Yasushi Iwaoka,Kazuhisa Hirayama,Seiji Nagata,Kenji Takai
出处
期刊:The American Journal of Gastroenterology [American College of Gastroenterology]
卷期号:103 (5): 1210-1216 被引量:100
标识
DOI:10.1111/j.1572-0241.2007.01714.x
摘要

BACKGROUND In human blood, two monocyte populations exist, CD14++CD16− classical monocytes and CD14+CD16+ proinflammatory monocytes, which account for about 10% of total monocytes, but can expand to promote inflammatory conditions. CD14+CD16+ monocytes produce large amounts of inflammatory cytokines including TNF-α and IL-1. Adacolumn adsorptive carriers adsorb from the blood in the column most of the monocytes/macrophages and granulocytes and this has been associated with clinical efficacy in patients with active inflammatory bowel disease (IBD). This study was to investigate the CD14+CD16+ monocyte profile in patients with IBD and the impact of Adacolumn on this proinflammatory phenotype. METHODS A total of 58 patients with ulcerative colitis (UC, N = 37) or Crohn's disease (CD, N = 21) together with 11 healthy controls were included in this study. Peripheral blood CD14+CD16+ monocytes were determined by three-color immunofluorescence and flow cytometry. RESULTS The percentage of CD14+CD16+ monocytes in patients with active CD was significantly (P= 0.0089) higher than the level in the control group, in patients with quiescent CD (P= 0.0419) or quiescent UC (P= 0.0063). Further, the percentage of CD14+CD16+ monocytes in patients with active UC who were on prednisolone (PSL) was less than the level in those not on PSL (P < 0.0001), thus PSL might have a suppressive effect on CD14+CD16+ monocytes. Patients with active IBD were each given up to 10 Adacolumn granulocye/monocyte adsorption (GMA) sessions over an 8-wk period. The percentage of CD14+CD16+ monocytes decreased dramatically (P= 0.0077 in UC and P= 0.0117 in CD) compared with entry levels. CONCLUSIONS A significant reduction in peripheral CD14+CD16+ monocytes by GMA should mitigate the inflammatory drive and contribute to the clinical efficacy of this procedure. Reduction of CD14+CD16+ monocytes by corticosteroids was also seen. Hence, corticosteroids should enhance the efficacy of GMA. This is the first report on CD14+CD16+ monocytes being decreased by Adacolumn GMA in patients with IBD.

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