Haruta J, Kusugami K, Kuroiwa A, Ina K, Shinoda M, Morise K, Iokawa H, Morita M, Ishihara A, Sarai S
First Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Am J Gastroenterol. 1992 Apr;87(4):448-54.
Phenotypic and functional analysis was performed with lamina propria mononuclear cells (LPMCs) isolated from colonoscopic biopsies in 27 patients with ulcerative colitis (UC). The proportion of T lymphocytes displaying HLA-DR antigens, interleukin 2 (IL-2) receptor, and transferrin receptor was greater in active UC than in control diseases. When LPMCs were cultured with IL-2 or phytohemagglutinin for 72 h, there were no significant differences in the proportion of cells bearing these activation markers between active UC and controls. The proportion of CD56+ cells and lymphokine-activated killer (LAK) cell activity was lower in LPMCs from active UC than in control cells, and depletion of CD56+ cells from control lamina propria cells essentially eliminated LAK cell activity. Mucosal T lymphocytes may be activated in vivo during active inflammation in UC, and lower levels of intestinal LAK cell activity may be related to the decrease of CD56+ cells under these conditions.
对27例溃疡性结肠炎(UC)患者结肠镜活检分离出的固有层单核细胞(LPMC)进行了表型和功能分析。活动性UC中显示HLA-DR抗原、白细胞介素2(IL-2)受体和转铁蛋白受体的T淋巴细胞比例高于对照疾病。当LPMC与IL-2或植物血凝素培养72小时时,活动性UC与对照之间携带这些活化标记的细胞比例无显著差异。活动性UC的LPMC中CD56+细胞比例和淋巴因子激活的杀伤(LAK)细胞活性低于对照细胞,从对照固有层细胞中去除CD56+细胞基本消除了LAK细胞活性。黏膜T淋巴细胞可能在UC活动性炎症期间在体内被激活,在这些情况下肠道LAK细胞活性水平较低可能与CD56+细胞减少有关。