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肾炎因子:一种新的定量检测方法的描述及肾小球肾炎的研究结果

Nephritic factor: Description of a new quantitative assay and findings in glomerulonephritis.

作者信息

Border W A, Wilson C B, Götze O

出版信息

Kidney Int. 1976 Oct;10(4):311-8. doi: 10.1038/ki.1976.114.

DOI:10.1038/ki.1976.114
PMID:62864
Abstract

A sensitive quantitative test for nephritic factor (NF) in human serum is reported. The test is based on the capacity of NF to initiate fluid phase consumption of the third complement (C) component in the presence of magnesium ions (Mg++) and of factors of the alternative pathway of C activation. These factors as well as C3 and C5 were supplied by the incorporation of normal human serum (NHS) into the assay mixture. In order to prevent C3 (and C5) consumption via the Ca++- and Mg++-dependent classical pathway, the test was performed in the presence of the chelating agent Mg-ethylene bis (oxyethylene-nitrilo) tetraacetic acid (Mg EGTA) which interacts preferentially with Ca++. The Mg EGTA concentration was found to be critical, a final concentration of 5 mM in the assay mixture being required for optimal results. By its heat stability (54 degrees to 56 degrees C, 30 min), NF could be distinguished from other, heat-labile NF-like factors. The NF test was applied to five categories of patients with glomerulonephritis (GN). Heat-stable NF activity was found in seven of 17 sera in the membranoproliferative glomerulonephritis (MPGN) group. Two of the 12 acute poststreptococcal GN sera had NF-like activity which disappeared upon heating. Serum C3 and proactivator (PA) concentrations varied widely in all groups but a clear positive relationship was found between the presence of NF and low serum C3 concentrations in MPGN. Renal immunofluorescence in MPGN indicated a lesser amount of lg deposited in glomeruli from patients with NF when compared to the NF-negative patients. Both groups had heavy C3 deposits. The availability of a sensitive, quantitative assay for NF may help to provide further insight into the various pathogenic mechanisms in different forms of MPGN.

摘要

本文报道了一种检测人血清中肾炎因子(NF)的灵敏定量试验。该试验基于NF在镁离子(Mg++)及补体激活替代途径相关因子存在的情况下,启动第三补体(C)成分液相消耗的能力。这些因子以及C3和C5通过在检测混合物中加入正常人血清(NHS)来提供。为防止通过依赖钙离子(Ca++)和镁离子的经典途径消耗C3(及C5),试验在螯合剂乙二醇双(氧乙腈)四乙酸镁(Mg EGTA)存在的情况下进行,Mg EGTA优先与Ca++相互作用。发现Mg EGTA浓度至关重要,检测混合物中最终浓度为5 mM时可获得最佳结果。通过其热稳定性(54℃至56℃,30分钟),NF可与其他热不稳定的类NF因子相区分。NF试验应用于五类肾小球肾炎(GN)患者。在膜增生性肾小球肾炎(MPGN)组的17份血清中,有7份发现了热稳定的NF活性。12份急性链球菌感染后GN血清中有2份具有类NF活性,加热后消失。所有组中血清C3和前激活剂(PA)浓度差异很大,但在MPGN中发现NF的存在与低血清C3浓度之间存在明显的正相关。MPGN的肾脏免疫荧光显示,与NF阴性患者相比,NF阳性患者肾小球中沉积的免疫球蛋白(lg)量较少。两组均有大量C3沉积。一种用于NF的灵敏定量检测方法的可用性可能有助于进一步深入了解不同形式MPGN的各种致病机制。

相似文献

1
Nephritic factor: Description of a new quantitative assay and findings in glomerulonephritis.肾炎因子:一种新的定量检测方法的描述及肾小球肾炎的研究结果
Kidney Int. 1976 Oct;10(4):311-8. doi: 10.1038/ki.1976.114.
2
[Complement and nephritic activity in membranoproliferative glomerulonephritis].[膜增生性肾小球肾炎中的补体与肾炎活性]
Arch Fr Pediatr. 1979 Nov;36(9 Suppl):LXIV-LXXIV.
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C3 metabolism in acute glomerulonephritis: implications for sites of complement activation.
Kidney Int. 1984 Jun;25(6):937-41. doi: 10.1038/ki.1984.113.
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Differences between membranoproliferative glomerulonephritis types I and III in clinical presentation, glomerular morphology, and complement perturbation.膜增生性肾小球肾炎I型和III型在临床表现、肾小球形态及补体紊乱方面的差异。
Am J Kidney Dis. 1987 Feb;9(2):115-20. doi: 10.1016/s0272-6386(87)80088-4.
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A hemolytic method for the measurement of nephritic factor.一种用于测量肾炎因子的溶血方法。
J Immunol Methods. 2008 Jun 1;335(1-2):1-7. doi: 10.1016/j.jim.2007.12.001. Epub 2007 Dec 31.
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Membranoproliferative glomerulonephritis. Localization of early components of complement in glomerular deposits.膜增生性肾小球肾炎。补体早期成分在肾小球沉积物中的定位。
Am J Pathol. 1976 Aug;84(2):283-98.
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C3 nephritic factor and C4 nephritic factor in the serum of two patients with hypocomplementaemic membranoproliferative glomerulonephritis.两名低补体血症性膜增生性肾小球肾炎患者血清中的C3肾炎因子和C4肾炎因子
Clin Exp Immunol. 1989 Apr;76(1):82-5.
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[Partial lipodystrophy, hypocomplementemia and glomerulonephritis].[部分性脂肪营养不良、低补体血症和肾小球肾炎]
Arch Fr Pediatr. 1977 Aug-Sep;34(7 Suppl):CXCVII-CCXII.
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Membranoproliferative glomerulonephritis and C3 glomerulonephritis: frequency, clinical features, and outcome in children.膜增生性肾小球肾炎和C3肾小球肾炎:儿童中的发病率、临床特征及预后
Nephrology (Carlton). 2015 Apr;20(4):286-92. doi: 10.1111/nep.12382.
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Discordant renal histopathologic findings and complement profiles in membranoproliferative glomerulonephritis type III.III型膜增生性肾小球肾炎中不一致的肾脏组织病理学表现和补体谱。
Am J Kidney Dis. 1996 Dec;28(6):804-10. doi: 10.1016/s0272-6386(96)90379-0.

引用本文的文献

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Causes of alternative pathway dysregulation in dense deposit disease.致密物沉积病中旁路途径调控异常的原因。
Clin J Am Soc Nephrol. 2012 Feb;7(2):265-74. doi: 10.2215/CJN.07900811. Epub 2012 Jan 5.
2
Complement activation by circulating serum factors in human glomerulonephritis.人肾小球肾炎中循环血清因子介导的补体激活。
Clin Exp Immunol. 1985 Feb;59(2):276-84.
3
Heterogeneity of nephritic factor and its identification as an immunoglobulin.肾炎因子的异质性及其作为免疫球蛋白的鉴定
Proc Natl Acad Sci U S A. 1977 Sep;74(9):3980-3. doi: 10.1073/pnas.74.9.3980.