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患有特发性迁延性腹泻和肠上皮细胞自身抗体的儿童空肠活检组织中的HLA产物表达及淋巴细胞亚群

HLA product expression and lymphocyte subpopulations in jejunum biopsies of children with idiopathic protracted diarrhoea and enterocyte autoantibodies.

作者信息

Mirakian R, Hill S, Richardson A, Milla P J, Walker-Smith J A, Bottazzo G F

机构信息

Department of Immunology, Middlesex Hospital Medical School, London.

出版信息

J Autoimmun. 1988 Jun;1(3):263-77. doi: 10.1016/0896-8411(88)90032-7.

DOI:10.1016/0896-8411(88)90032-7
PMID:3266956
Abstract

Mature enterocytes from normal human small intestine express HLA Class II molecules, whereas the immature enterocytes of the crypts are devoid of these products. By the use of the Avidin/Biotin immunofluorescence technique, we examined HLA Class I and II expression on cryostat sections of jejunum biopsies from 10 children with idiopathic protracted diarrhoea (IPD) and circulating enterocyte autoantibodies (Ec-Abs). The results were compared with those obtained on gut specimens from nine children with protracted diarrhoea but no evidence of circulating Ec-Abs and from one child affected by gluten-sensitive enteropathy. HLA Class I expression was similar in control and pathological specimens but jejunum biopsies from children with IPD and high titres of Ec-Abs (greater than or equal to 1:64) showed 'inappropriate' Class II molecule expression in the crypt epithelial cells. This was in contrast with normal or only mildly increased Class II reactivity in the mature villi enterocytes. Conversely, jejunum biopsies from children with IPD but with low levels of Ec-Abs (less than or equal to 1:4) possessed a moderate but distinct decrease of Class II expression in mature enterocytes with a decreased number of CD3 and CD8 intraepithelial lymphocytes. It is speculated that quantitative and qualitative variations of HLA product expression in the gut epithelium of children with IPD could reflect the severity of the autoimmune process underlying the clinical picture and point to heterogeneities within the autoimmune enteropathy syndrome.

摘要

正常人类小肠的成熟肠上皮细胞表达HLA - II类分子,而隐窝中的未成熟肠上皮细胞则不表达这些产物。通过抗生物素蛋白/生物素免疫荧光技术,我们检测了10例患有特发性慢性腹泻(IPD)和循环肠上皮细胞自身抗体(Ec - Abs)的儿童空肠活检组织冰冻切片上的HLA - I类和II类表达情况。将结果与9例患有慢性腹泻但无循环Ec - Abs证据的儿童以及1例患有麸质敏感性肠病的儿童的肠道标本检测结果进行了比较。对照组和病理标本中的HLA - I类表达相似,但IPD患儿且Ec - Abs滴度高(大于或等于1:64)的空肠活检组织在隐窝上皮细胞中显示出“不适当的”II类分子表达。这与成熟绒毛肠上皮细胞中正常或仅轻度增加的II类反应性形成对比。相反,IPD患儿但Ec - Abs水平低(小于或等于1:4)的空肠活检组织在成熟肠上皮细胞中II类表达有中度但明显的降低,且上皮内CD3和CD8淋巴细胞数量减少。据推测,IPD患儿肠道上皮中HLA产物表达的定量和定性变化可能反映了临床症状背后自身免疫过程的严重程度,并指出自身免疫性肠病综合征内的异质性。

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