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本文引用的文献

1
Antibody-negative Goodpasture's disease.抗体阴性的肺出血肾炎综合征
NDT Plus. 2010 Jun;3(3):253-256. doi: 10.1093/ndtplus/sfq003. Epub 2010 Mar 30.
2
Frequently relapsing anti-glomerular basement membrane antibody disease with changing clinical phenotype and antibody characteristics over time.频繁复发的抗肾小球基底膜抗体病,其临床表型和抗体特征随时间变化。
Clin Kidney J. 2016 Oct;9(5):661-4. doi: 10.1093/ckj/sfw048. Epub 2016 Jun 19.
3
Multiple recurrences of anti-glomerular basement membrane disease with variable antibody detection: can the laboratory be trusted?抗肾小球基底膜病多次复发伴抗体检测结果各异:实验室检测结果可靠吗?
Clin Kidney J. 2016 Oct;9(5):657-60. doi: 10.1093/ckj/sfw038. Epub 2016 May 17.
4
Factors Associated With Pathogenicity of Anti-Glomerular Basal Membrane Antibodies: A Case Report.抗肾小球基底膜抗体致病性相关因素:一例报告
Medicine (Baltimore). 2016 May;95(19):e3654. doi: 10.1097/MD.0000000000003654.
5
The clinicopathologic characteristics and outcome of atypical anti-glomerular basement membrane nephritis.非典型抗肾小球基底膜肾炎的临床病理特征和转归。
Kidney Int. 2016 Apr;89(4):897-908. doi: 10.1016/j.kint.2016.02.001.
6
Atypical anti-glomerular basement membrane disease.非典型抗肾小球基底膜病
Clin Kidney J. 2016 Apr;9(2):211-21. doi: 10.1093/ckj/sfv140. Epub 2015 Dec 30.
7
Seronegative anti-GBM Disease with Coexistent ANCA Positivity.血清阴性抗肾小球基底膜病合并ANCA阳性
Bull Hosp Jt Dis (2013). 2014;72(4):301-4.
8
Autoimmunity to the alpha 3 chain of type IV collagen in glomerulonephritis is triggered by 'autoantigen complementarity'.肾小球肾炎中针对IV型胶原α3链的自身免疫是由“自身抗原互补性”引发的。
J Autoimmun. 2015 May;59:8-18. doi: 10.1016/j.jaut.2015.01.003. Epub 2015 Apr 2.
9
Chapter 14: Anti-glomerular basement membrane antibody glomerulonephritis.第14章:抗肾小球基底膜抗体肾小球肾炎。
Kidney Int Suppl (2011). 2012 Jun;2(2):240-242. doi: 10.1038/kisup.2012.27.
10
Circulating anti-glomerular basement membrane antibodies with predominance of subclass IgG4 and false-negative immunoassay test results in anti-glomerular basement membrane disease.循环中抗肾小球基底膜抗体以 IgG4 亚类为主且抗肾小球基底膜病免疫检测结果呈假阴性。
Am J Kidney Dis. 2014 Feb;63(2):289-93. doi: 10.1053/j.ajkd.2013.08.032. Epub 2013 Nov 1.

非典型抗肾小球基底膜病:经验教训

Atypical anti-glomerular basement membrane disease: lessons learned.

作者信息

Glassock Richard J

机构信息

David Geffen School of Medicine at UCLA , Laguna Niguel, Los Angeles, CA , USA.

出版信息

Clin Kidney J. 2016 Oct;9(5):653-6. doi: 10.1093/ckj/sfw068. Epub 2016 Jul 28.

DOI:10.1093/ckj/sfw068
PMID:27679709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5036901/
Abstract

Anti-glomerular basement membrane (GBM) disease usually pursues a self-limited course, at least from the immunological perspective. In addition, circulating antibodies to cryptic, conformational epitopes within the NC1 domain of the alpha 3 chain of Type IV Collagen are commonly found at the zenith of the clinical disease. However, exceptions to these general rules do occur, as exemplified by two remarkable cases reported in this issue of the Clinical Kidney Journal. The possible explanations for and the lessons learned from these uncommon occurrences are discussed in this short commentary.

摘要

抗肾小球基底膜(GBM)疾病通常呈自限性病程,至少从免疫学角度来看是这样。此外,在临床疾病的高峰期,通常会发现针对IV型胶原α3链NC1结构域内隐蔽性构象表位的循环抗体。然而,这些一般规律也有例外情况,本期《临床肾脏杂志》报道的两个显著病例就是例证。本简短评论将讨论这些罕见病例出现的可能原因及从中吸取的经验教训。