Bookman M A, Bull D M
Gastroenterology. 1979 Sep;77(3):503-10.
Immunologic characteristics of intestinal mucosal lymphoid cells from patients with inflammatory bowel disease and controls have been compared. Mononuclear cells isolated by enzymatic means from intestinal tissues involved with inflammatory bowel disease were present in greater numbers, with increased proportions of macrophages and B-lymphocytes, particularly cells bearing intrinsic membrane immunoglobulin G. Synthesis of immunoglobulin G, measured by radioimmunoassay, was increased tenfold in inflammatory bowel disease, while immunoglobulin A synthesis per 10(6) cells was unchanged. "Null" or K-lymphocytes were absent from all populations, and antibody-dependent cellular cytotoxicity (a K-cell-mediated function) was not demonstrable. Taken together, the results fail to support a role for antibody-dependent cellular cytotoxicity or a defect in secretory immunoglobulin A, but rather focus attention upon possible forms of immunoglobulin G-mediated tissue damage in the pathogenesis or perpetuation of inflammatory bowel disease.
对炎症性肠病患者和对照组的肠道黏膜淋巴细胞的免疫特性进行了比较。通过酶法从患有炎症性肠病的肠道组织中分离出的单核细胞数量更多,巨噬细胞和B淋巴细胞的比例增加,尤其是携带内在膜免疫球蛋白G的细胞。通过放射免疫测定法测得,炎症性肠病中免疫球蛋白G的合成增加了10倍,而每10(6)个细胞中免疫球蛋白A的合成没有变化。所有群体中均不存在“无标记”或K淋巴细胞,且未证实抗体依赖性细胞毒性(一种K细胞介导的功能)。综上所述,这些结果不支持抗体依赖性细胞毒性的作用或分泌性免疫球蛋白A的缺陷,而是将注意力集中在炎症性肠病发病机制或持续存在中免疫球蛋白G介导的组织损伤的可能形式上。