肠病相关T细胞淋巴瘤。

Cancer surveys Pub Date : 1997-01-01
D H Wright
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摘要

肠病相关T细胞淋巴瘤(EATCL)是乳糜泻最严重的并发症。HLA基因分型显示,EATCL患者存在与乳糜泻相关的DQA1*0501、DQB1*0201表型。其他可能与成人发病乳糜泻相关的HLA-DR/DQ等位基因似乎是淋巴瘤发展的额外危险因素。腹腔疾病患者的小肠黏膜和EATCL患者的肠病性肠中发现小肠上皮内细胞毒性T细胞数量增加。EATCL的肿瘤细胞具有上皮内细胞毒性T细胞的免疫表型,可能表现为上皮性。T细胞受体基因和免疫组织化学分析表明,远离肿瘤的肠黏膜含有小T细胞克隆群体,通常与高级别T细胞淋巴瘤具有相同的克隆。大多数慢性溃疡性肠炎病例可能是同一疾病过程的一部分。慢性溃疡性肠炎和肠病相关T细胞淋巴瘤的溃疡可能是由于细胞毒性T细胞和肿瘤细胞释放细胞溶解酶所致。这些发现表明,EATCL出现在乳糜泻的背景下,可能在麦胶蛋白肽的抗原驱动下,从上皮内淋巴细胞增生到低级别淋巴瘤发展到高级别肿瘤。这些肽可能由携带乳糜泻相关HLA-DQ等位基因的上皮细胞直接呈递给上皮内细胞毒性T细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enteropathy associated T cell lymphoma.

Enteropathy associated T cell lymphoma (EATCL) is the most serious complication of coeliac disease. HLA genotyping shows that patients with EATCL have the coeliac disease associated DQA1*0501, DQB1*0201 phenotype. Other HLA-DR/DQ alleles that may be associated with adult onset coeliac disease appear to represent additional risk factors for lymphoma development. Increased numbers of small intestinal intraepithelial cytotoxic T cells are found in the small intestinal mucosa of patients with coeliac disease and in the enteropathic bowel of patients with EATCL. The neoplastic cells of EATCL have the immunophenotype of intraepithelial cytotoxic T cells and may exhibit epitheliotropism. Analysis of T cell receptor genes and immunohistochemistry have shown that the intestinal mucosa distant from the tumour contains clonal populations of small T cells, often of the same clone as the high grade T cell lymphoma. Most cases of chronic ulcerative enteritis are probably part of the same disease process. The ulceration seen in chronic ulcerative enteritis and in enteropathy associated T cell lymphoma may be due to the release of cytolytic enzymes by cytotoxic T cells and tumour cells. These findings suggest that EATCL arises in the setting of coeliac disease and evolves from intraepithelial lymphocytosis through low grade lymphoma to a high grade tumour, possibly under antigen drive from gliadin peptides. These peptides may be presented to the intraepithelial cytotoxic T cells directly by epithelial cells bearing the coeliac disease associated HLA-DQ alleles.

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