Augustin Merja T, Kokkonen Jorma, Karttunen Tuomo J
Department of Pathology, University of Oulu, Oulu, Finland.
Scand J Gastroenterol. 2005 Dec;40(12):1398-406. doi: 10.1080/00365520510023765.
Pathogenetic mechanisms of cow's milk protein-sensitive enteropathy (CMSE) are poorly defined, but elevated serum granzyme levels and an increase in duodenal intraepithelial lymphocytes (IELs) expressing TIA-1 suggest the involvement of abnormal lymphocyte cytotoxicity. To evaluate cytotoxicity in CMSE we analysed the expression of cytotoxic granule components in duodenal IELs. For comparison, we studied subjects with coeliac disease (CD), in which lymphocyte cytotoxicity is pathogenically important.
Fifty-four children were examined by endoscopy for gastrointestinal complaints. Twenty-one subjects had a final diagnosis of CMSE, 15 children had untreated CD and 18 controls showed no definite gastrointestinal disease. Mucosal samples furnished from the bulb and descending duodenum were stained for CD3, perforin, granzymes A and B and TIA-1.
In both CMSE and CD, increase of mid-duodenal TIA-1, perforin and granzyme A expressing IELs was seen, the counts in CD being much higher, and increased expression was also seen in the bulb. Granzyme B expression was increased only in CD. In CMSE, no evidence of villous atrophy was seen.
Increase in duodenal IELs expressing cytotoxic granules is a characteristic feature in CMSE, although to a lesser degree than in CD. Cytotoxicity is suggested to be involved in the pathogenesis of intestinal dysfunction in CMSE, but based on the absence of villous abnormalities may not be mainly targeted to enterocytes. The mechanisms leading to the accumulation of these cells in CMSE need further investigation.
牛奶蛋白敏感性肠病(CMSE)的发病机制尚不清楚,但血清颗粒酶水平升高以及十二指肠上皮内淋巴细胞(IEL)中表达TIA-1的细胞增多提示存在异常淋巴细胞细胞毒性。为评估CMSE中的细胞毒性,我们分析了十二指肠IEL中细胞毒性颗粒成分的表达。作为对照,我们研究了乳糜泻(CD)患者,其中淋巴细胞细胞毒性在发病机制中起重要作用。
对54名因胃肠道不适接受内镜检查的儿童进行了研究。21名受试者最终诊断为CMSE,15名儿童患有未经治疗的CD,18名对照者未发现明确的胃肠道疾病。取自十二指肠球部和降部的黏膜样本进行了CD3、穿孔素、颗粒酶A和B以及TIA-1染色。
在CMSE和CD中,均可见十二指肠中部表达TIA-1、穿孔素和颗粒酶A的IEL增多,CD中的计数更高,在十二指肠球部也可见表达增加。颗粒酶B的表达仅在CD中增加。在CMSE中,未发现绒毛萎缩的证据。
十二指肠中表达细胞毒性颗粒的IEL增多是CMSE的一个特征,尽管程度低于CD。细胞毒性被认为参与了CMSE肠道功能障碍的发病机制,但基于绒毛无异常,可能并非主要针对肠上皮细胞。导致这些细胞在CMSE中积聚的机制需要进一步研究。