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一名患有膜性肾病和双侧肾盂输尿管狭窄的患者体内存在针对刷状缘抗原(Fx1A)的循环抗体。与特发性膜性肾病的比较。

Presence of circulating antibodies against brush border antigens (Fx1A) in a patient with membranous nephropathy and bilateral pyeloureteral stenosis. Comparison with idiopathic membranous nephropathy.

作者信息

González-Cabrero J, de Nicolas R, Ortíz A, Mampaso F, Hernando L, Egido J

机构信息

Fundación Jiménez Díaz, Universidad Autónoma, CSIC, Madrid, Spain.

出版信息

Nephrol Dial Transplant. 1992;7(4):293-9. doi: 10.1093/oxfordjournals.ndt.a092131.

DOI:10.1093/oxfordjournals.ndt.a092131
PMID:1317518
Abstract

In a patient with membranous nephropathy and bilateral pyeloureteral stenosis with hydronephrosis, we examined the possibility that an increase in the intratubular pressure could facilitate the passage of the Fx1A antigens to the circulation. Elevated serum anti-Fx1A antibodies were detected in this particular patient by ELISA on three occasions during the disease follow-up, even though he was in clinical remission. These antibodies reacted in vitro with the tubular brush border of a normal human kidney. The anti-Fx1A antibodies isolated from the patient's sera by affinity chromatography competed with the rabbit anti-Fx1A antisera binding to plates coated with human Fx1A antigen. In immunoblotting studies the isolated specific IgG antibodies from that patient reacted with a 180 kDa antigen of the human Fx1A and with less intensity with 75 kDa and 50-55 kDa polypeptides. In none of 12 patients with idiopathic membranous nephropathy could the circulating anti-Fx1A antibodies be demonstrated. On the whole, this particular case suggests that on some occasions increased intratubular pressure could cause the release of Fx1A antigens, facilitating an autologous immunocomplex nephritis. These antigens, by contrast, do not seem to play any role in most cases of membranous nephropathy in man.

摘要

在一名患有膜性肾病且双侧肾盂输尿管狭窄伴肾积水的患者中,我们研究了肾小管内压力升高是否可能促进Fx1A抗原进入循环的可能性。在该疾病随访期间,通过ELISA在该特定患者身上三次检测到血清抗Fx1A抗体升高,尽管他处于临床缓解期。这些抗体在体外与人正常肾脏的肾小管刷状缘发生反应。通过亲和层析从患者血清中分离出的抗Fx1A抗体与兔抗Fx1A抗血清竞争结合包被有人Fx1A抗原的平板。在免疫印迹研究中,从该患者分离出的特异性IgG抗体与人类Fx1A的180 kDa抗原发生反应,并与75 kDa以及50 - 55 kDa多肽发生较弱反应。在12例特发性膜性肾病患者中均未检测到循环抗Fx1A抗体。总体而言,这个特殊病例表明,在某些情况下,肾小管内压力升高可能导致Fx1A抗原释放,从而引发自身免疫复合物性肾炎。相比之下,这些抗原在大多数人类膜性肾病病例中似乎不起任何作用。

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Presence of circulating antibodies against brush border antigens (Fx1A) in a patient with membranous nephropathy and bilateral pyeloureteral stenosis. Comparison with idiopathic membranous nephropathy.一名患有膜性肾病和双侧肾盂输尿管狭窄的患者体内存在针对刷状缘抗原(Fx1A)的循环抗体。与特发性膜性肾病的比较。
Nephrol Dial Transplant. 1992;7(4):293-9. doi: 10.1093/oxfordjournals.ndt.a092131.
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