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小儿乳糜泻中的淋巴细胞性胃炎——上皮内淋巴细胞成分的免疫组织化学研究

Lymphocytic gastritis in pediatric celiac disease -- immunohistochemical study of the intraepithelial lymphocytic component.

作者信息

Drut Ricardo, Drut Rosa M

机构信息

Department of Pathology, Hospital de Nińos 'Superiora Sor Mar a Ludovica', La Plata, Argentina.

出版信息

Med Sci Monit. 2004 Jan;10(1):CR38-42.

Abstract

BACKGROUND

Lymphocytic gastritis (LG) is defined by the recognition of >25 intraepithelial lymphocytes (IEL) per 100 surface epithelial cells. Approximately 50% of children with celiac disease (CD) present LG, which mainly involves the gastric antrum and disappears after a gluten-free diet. This intraepithelial population of lymphocytes has not been immunophenotypically characterized for this age group.

MATERIAL/METHODS: We immunohistochemically analyzed 5 formalin-fixed, paraffin embedded biopsies of LG in children with untreated celiac disease using a panel of antibodies. All patients were diagnosed on the bases of clinical, laboratory and histopathological data.

RESULTS

All showed similar results. IEL proved to be CD45RO, CD3, CD7, CD8, and Tia-1 positive, while CD4, CD20, CD79a, CD56, CD57, granzyme B, perforin, TCR gamma-delta, TCR beta (V-19), CD95 (FAS), CD95-L (FAS-L) and HLA II were negative. Many IEL were in apoptosis. CD45RO, CD3 and CD7 presented as membranous staining, while Tia-1 resulted in intracytoplasmic granular brown dots. In 3 cases there were rare lymphocytes with granzyme B-positive granules localized to the lamina propria. None presented Helicobacter pylori -like organisms at the luminal surface.

CONCLUSIONS

LG associated with CD in children contains a peculiar CD8+ intraepithelial T-lymphocyte population which immunohistochemically lacks perforin and granzyme B, undergoes apoptosis, and is not associated with substantial damage to the epithelial cells. Our results fit with those reported in adults except for the negative results for granzyme B. The findings appear disparate from the ones described in the duodeno-jejunal mucosa in untreated celiac disease.

摘要

背景

淋巴细胞性胃炎(LG)的定义为每100个表面上皮细胞中存在超过25个上皮内淋巴细胞(IEL)。约50%的乳糜泻(CD)患儿存在LG,主要累及胃窦,无麸质饮食后可消失。该年龄组的这种上皮内淋巴细胞群体尚未进行免疫表型特征分析。

材料/方法:我们使用一组抗体对5例未经治疗的乳糜泻患儿的LG福尔马林固定、石蜡包埋活检组织进行了免疫组织化学分析。所有患者均根据临床、实验室和组织病理学数据确诊。

结果

所有结果相似。IEL被证明CD45RO、CD3、CD7、CD8和Tia-1呈阳性,而CD4、CD20、CD79a、CD56、CD57、颗粒酶B、穿孔素、TCRγ-δ、TCRβ(V-19)、CD95(FAS)、CD95-L(FAS-L)和HLA II呈阴性。许多IEL处于凋亡状态。CD45RO、CD3和CD7呈膜性染色,而Tia-1表现为胞质内颗粒状棕色点。3例中固有层有罕见的颗粒酶B阳性颗粒的淋巴细胞。管腔表面均未发现幽门螺杆菌样生物体。

结论

儿童中与CD相关的LG含有一种特殊的CD8+上皮内T淋巴细胞群体,免疫组织化学显示其缺乏穿孔素和颗粒酶B,会发生凋亡,且与上皮细胞的实质性损伤无关。除颗粒酶B结果为阴性外,我们的结果与成人报道的结果相符。这些发现与未经治疗的乳糜泻十二指肠-空肠黏膜中描述的结果不同。

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