Kusugami K, Haruta J, Ieda M, Shinoda M, Ando T, Kuroiwa A, Ina K, Iokawa H, Ishihara A, Sarai S
First Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Dig Dis Sci. 1995 Jan;40(1):198-210. doi: 10.1007/BF02063967.
Intestinal T-cell lines were generated from lamina propria mononuclear cells isolated from colonoscopic biopsies in ulcerative colitis patients and controls. In both ulcerative colitis and controls, expanded cells were constituted largely by T-cell receptor alpha beta+, CD4+, CD45RA- (helper), and CD8+, CD11b- (cytotoxic) phenotypes. T-cell receptor V beta gene usage was not significantly changed after cell expansion and no difference was observed between ulcerative colitis and controls. Ulcerative colitis cells, especially those derived from the patients with long-standing disease, showed significantly higher levels of cytotoxicity against the target cells, including those of colonic epithelial origin, and enhanced production of tumor necrosis factor-alpha and interferon-gamma after short incubation with anti-CD3 antibody. Generation of T-cell lines from colonoscopic biopsy specimens may be useful for detailed functional characterization of locally infiltrating T cells in ulcerative colitis patients.
肠道T细胞系由溃疡性结肠炎患者和对照者结肠镜活检分离的固有层单核细胞生成。在溃疡性结肠炎患者和对照者中,扩增的细胞主要由T细胞受体αβ+、CD4+、CD45RA-(辅助性)以及CD8+、CD11b-(细胞毒性)表型组成。细胞扩增后T细胞受体Vβ基因的使用情况没有显著变化,溃疡性结肠炎患者和对照者之间也未观察到差异。溃疡性结肠炎细胞,尤其是来自患有长期疾病患者的细胞,对靶细胞(包括结肠上皮来源的靶细胞)表现出显著更高的细胞毒性水平,并且在与抗CD3抗体短时间孵育后,肿瘤坏死因子-α和干扰素-γ的产生增加。从结肠镜活检标本中生成T细胞系可能有助于对溃疡性结肠炎患者局部浸润T细胞进行详细的功能表征。