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风湿性多肌痛和/或巨细胞(颞)动脉炎患者的一种新的血清学反应:通过间接免疫荧光检测到补体C4和C3成分在大鼠肾脏结构上的沉积。

A new serological reaction in patients with polymyalgia rheumatica and/or giant cell (temporal) arteritis: deposition of complement C4 and C3 components on rat kidney structures detected by indirect immunofluorescence.

作者信息

Vaith P, Maas D, von Stackelberg G, Peter H H

出版信息

Rheumatol Int. 1986;6(6):255-61. doi: 10.1007/BF00541316.

Abstract

Using indirect immunofluorescence deposition of complement C4 and C3 components to rat kidney medullary structures was demonstrated. This serological reaction (C4/C3-IFT) is regularly obtained with fresh sera of patients suffering from active polymyalgia rheumatica (PMR) and/or giant cell (temporal) arteritis (GCA). Sera of normal controls and of steroid-treated PMR and/or GCA patients in clinical remission have a negative C4/C3-IFT reaction. A positive conversion of the test in steroid-treated patients indicates enhanced disease activity. Because of its technical simplicity, C4/C3-IFT can be routinely used first, as a reliable serological marker in the primary diagnosis of PMR and/or GCA and second, as a sensitive criterion of disease activity in these patients. C4/C3-IFT reactivity is, however, not specific for GCA and/or PMR. Various systemic inflammatory diseases may have a positive reaction as well (e.g., certain viral and bacterial infections, malignant tumors, vasculitides, inflammatory joint diseases of different etiology). Recent experimental findings suggest that C-reactive protein (CRP) in patients' sera mediates an activation of the classical complement pathway resulting in a deposition of C4 and C3 complement components to certain rat kidney structures.

摘要

已证实可利用间接免疫荧光法检测补体C4和C3成分在大鼠肾髓质结构中的沉积。这种血清学反应(C4/C3免疫荧光试验)在患有活动性风湿性多肌痛(PMR)和/或巨细胞(颞)动脉炎(GCA)的患者新鲜血清中经常出现。正常对照以及处于临床缓解期的接受类固醇治疗的PMR和/或GCA患者血清的C4/C3免疫荧光试验反应为阴性。接受类固醇治疗的患者试验结果呈阳性转变表明疾病活动增强。由于其技术操作简单,C4/C3免疫荧光试验首先可常规用作PMR和/或GCA初步诊断中的可靠血清学标志物,其次可作为这些患者疾病活动的敏感标准。然而,C4/C3免疫荧光试验反应并非GCA和/或PMR所特有。各种全身性炎症性疾病也可能出现阳性反应(例如,某些病毒和细菌感染、恶性肿瘤、血管炎、不同病因的炎性关节疾病)。最近的实验结果表明,患者血清中的C反应蛋白(CRP)介导经典补体途径的激活,导致C4和C3补体成分沉积于某些大鼠肾脏结构。

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