Choy M Y, Walker-Smith J A, Williams C B, MacDonald T T
Department of Paediatric Gastroenterology, St Bartholomew's Hospital, London.
Gut. 1990 Dec;31(12):1365-70. doi: 10.1136/gut.31.12.1365.
Many interleukin-2 receptor (CD25) bearing cells can be identified by alkaline phosphatase immunohistochemistry in the diseased intestinal lamina propria of children with Crohn's disease or ulcerative colitis, but rarely in normal intestine. In both diseases, the CD25+ cells are present as aggregates in the lamina propria below the epithelium, and constitute a large proportion of the lamina propria mononuclear cells. In Crohn's disease, but not ulcerative colitis, CD25+ cells are abundant in the submucosa. The CD25+ cells in Crohn's disease are 58-88% CD3+, CD4+, CD8-, indicating that they are T cells, whereas in ulcerative colitis the CD25+ cells are greater than 80% CD3-, CD4+, HLA-DR+, indicating that they are macrophages. Thus, differential expression of CD25 on T cells and macrophages serves to distinguish the immunologic lesions in ulcerative colitis and Crohn's disease.
通过碱性磷酸酶免疫组织化学方法可在患有克罗恩病或溃疡性结肠炎儿童的病变肠固有层中识别出许多携带白细胞介素-2受体(CD25)的细胞,但在正常肠道中却很少见。在这两种疾病中,CD25+细胞以上皮下方固有层中的聚集形式存在,并构成固有层单核细胞的很大一部分。在克罗恩病而非溃疡性结肠炎中,黏膜下层有大量CD25+细胞。克罗恩病中的CD25+细胞58 - 88%为CD3+、CD4+、CD8-,表明它们是T细胞,而在溃疡性结肠炎中,CD25+细胞大于80%为CD3-、CD4+、HLA-DR+,表明它们是巨噬细胞。因此,T细胞和巨噬细胞上CD25的差异表达有助于区分溃疡性结肠炎和克罗恩病中的免疫损伤。