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抗肾小球基底膜病中的叠加性肾小球免疫复合物

Superimposed glomerular immune complexes in anti-glomerular basement membrane disease.

作者信息

Savige J A, Dowling J, Kincaid-Smith P

机构信息

Department of Nephrology, Royal Melbourne Hospital, Melbourne, Australia.

出版信息

Am J Kidney Dis. 1989 Aug;14(2):145-53. doi: 10.1016/s0272-6386(89)80190-8.

Abstract

The association of anti-glomerular basement membrane (GBM) antibody-mediated glomerulonephritis and glomerular immune complexes is common and probably arises from a number of mechanisms. In the series, glomerular immune complexes were identified in 6 of 17 patients who initially presented with anti-GBM disease. In four cases, glomerular immune complexes were noted in renal biopsies obtained at clinical presentation; in the other two, they were first demonstrated seven and 28 months after presentation, when circulating anti-GBM antibody levels were undetectable. Circulating immune complexes were detected in only two of six patients, either 28 months before or 17 months after the demonstration of the glomerular membranous lesion. The association of glomerular immune complexes and anti-GBM disease may be coincidental with immunologically-unrelated immune complexes localizing in the GBM for physico-chemical reasons; or the presence of glomerular-bound anti-GBM antibodies may predispose to the deposition of molecules with particular affinity for these antibodies. One patient with glomerular immune complexes used heroin, which may be associated with immune complex formation and the development of glomerulonephritis; and one patient was subsequently thought to have systemic lupus erythematosus (SLE). An antecedent infection was found in two of the four patients who had glomerular complexes at presentation, but in only three of 13 with uncomplicated anti-GBM disease. Three of 6 patients with superimposed glomerular complexes had a history of exposure to organic solvents before the onset of disease, while none in the group with anti-GBM disease alone had.

摘要

抗肾小球基底膜(GBM)抗体介导的肾小球肾炎与肾小球免疫复合物的关联很常见,可能由多种机制引起。在该系列研究中,17例最初表现为抗GBM病的患者中有6例发现了肾小球免疫复合物。4例患者在临床表现时进行的肾活检中发现了肾小球免疫复合物;另外2例患者在临床表现后7个月和28个月首次发现,此时循环抗GBM抗体水平无法检测到。在6例患者中只有2例检测到循环免疫复合物,分别在肾小球膜性病变出现前28个月或出现后17个月。肾小球免疫复合物与抗GBM病的关联可能是巧合,即免疫无关的免疫复合物因物理化学原因定位于GBM;或者肾小球结合的抗GBM抗体的存在可能促使对这些抗体具有特殊亲和力的分子沉积。1例有肾小球免疫复合物的患者使用海洛因,这可能与免疫复合物形成和肾小球肾炎的发生有关;1例患者随后被认为患有系统性红斑狼疮(SLE)。在临床表现时有肾小球复合物的4例患者中有2例发现有前驱感染,但在13例单纯抗GBM病患者中只有3例有前驱感染。6例有叠加肾小球复合物的患者中有3例在疾病发作前有接触有机溶剂的病史,而单纯抗GBM病组中无一例有此病史。

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