【自身免疫性肠病累及肾脏】。

Annales de pediatrie Pub Date : 1993-02-01
R Habib, A Beziau, O Goulet, S Blanche, P Niaudet
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引用次数: 0

摘要

作者报告了一例以自身免疫性肠病为特征的婴儿,其特征为长期腹泻、新生儿胰岛素依赖型糖尿病和皮炎,并在4个月大时发展为肾病综合征。肾活检显示膜性肾小球肾炎(MGN), IgG在肾小管基底膜(TMB)呈线性沉积。间接免疫荧光法在患者血清中检测到抗肠细胞抗体、抗tmb抗体和抗肾刷边(BB)抗体。病人服用了各种免疫抑制药物,但都未能改善病情。在病程中,抗tbm抗体逐渐消失,而BB抗体持续存在。对文献的回顾表明,自身免疫性肠病累及肾脏并不罕见,有5例被报道为与MGN存在相关的肾病综合征。在这些病例中,4例MGN与抗tbm抗体的存在有关,其余1例与抗bb抗体有关。本病例报告表明,在人类病理中,针对BB蛋白的自身抗体,以及在实验模型中,可能是导致MGN发展的原因。提示肾BB蛋白与肠上皮蛋白之间有密切的关系(可能有共同的表位)。
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[Renal involvement in autoimmune enteropathies].

The authors report on a infant who presented with an auto-immune enteropathy characterized by the association of a protracted diarrhea, a neonatal insulin-dependent diabetes, and a dermatitis and who developed a nephrotic syndrome at 4 months of age. A renal biopsy showed a membranous glomerulonephritis (MGN) with IgG linear deposits along the tubular basement membranes (TMB). By indirect immunofluorescence anti-enterocyte antibodies together with anti-TMB antibodies and anti-renal brush border (BB) antibodies were found in the serum of the patient. The patient received various immunosuppressive drugs that failed to improve the disease. In the course of the disease the anti-TBM antibodies disappeared progressively but the BB antibodies persisted. A review of the literature indicates that renal involvement is not uncommon in auto-immune enteropathy and in 5 cases it has been reported as being characterized by a nephrotic syndrome related to the presence of a MGN. In 4 of these cases MGN was associated with the presence of anti-TBM antibodies and in the remaining one with anti-BB antibodies. This case report shows that in human pathology, auto-antibodies to BB proteins may, as well as in experimental models, be responsible for the development of a MGN. It suggests a close relationship (probably a common epitope) between the renal BB proteins and the proteins of the gut epithelium.

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