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[抗中性粒细胞胞浆抗体在血管炎中的诊断及致病意义]

[Diagnostic and pathogenic significance of antineutrophil cytoplasmic antibodies in vasculitides].

作者信息

Bartůnková J, Tesar V, Fucíková T, Janatková I, Zabka J, Krystůfková O, Rychlík I

机构信息

Oddĕlení klinické imunologie, 1. lékarské fakulty Univerzity Karlovy v Praze.

出版信息

Bratisl Lek Listy. 1995 Oct;96(10):528-33.

PMID:8620323
Abstract

OBJECTIVES

The study represents a complex report on diagnostic and pathogenic significance of antineutrophil cytoplasmic autoantibodies (ANCA). Our report is founded on the results of our clinical and experimental studies.

METHODS

ANCA was examined by indirect immunofluorescence, or ELISA-anti MPO. The data for evaluation of diagnostic ANCA associations were gained by means of questionnaires. The experimental part involved examination of the impact of sera containing ANCA and monoclonal antibodies (MoAb) against proteinase 3 and control MoaB specific for neutrophils.

RESULTS

Within the course of 1 year we have examined 1010 samples, ANCA was found in 65 patients: 26 cases of systemic vasculitis, 12 cases of other autoimmune diseases, 9 cases of isolated glomerulonephritis, 7 cases of inflammatory intestinal diseases, 6 cases of ophthalmic inflammatory diseases, and 6 cases of other diseases. Vasculitis of small vessels found in our group of patients are concomitted by ANCA positivity in 90% (Wegener's granulomatosis 15/16, Churg--Strauss's syndrome 3/5, MPA 9/9), vasculitis of medium vessels 12% (classical polyarteritis nodosa 1/2, Kawasaki disease 0/2, Henoch--Schönlein's purpura 0/4, Takayasu's arteritis 1/4). The ANCA-containing sera inhibit the candidacidal activity by 65% in average. THe inhibitory impact is yielded by anti-proteinase MoAb, in contrast to the control MoAb.

CONCLUSION

c-ANCA in high concentration is specific for active form of Wegener's granulomatosis, other types of ANCA in low titres are not of diagnostic value for vasculitis. ANCA is concomitted especially by small vessels vasculitis. The proved inhibition of microbicidal PMN activity by ANCA can participate in some clinical signs of immunodeficiencies in vasculitis. (Tab. 5, Ref. 18.).

摘要

目的

本研究是关于抗中性粒细胞胞浆自身抗体(ANCA)诊断及致病意义的综合报告。本报告基于我们的临床和实验研究结果。

方法

通过间接免疫荧光法或酶联免疫吸附测定法(ELISA)-抗髓过氧化物酶(MPO)检测ANCA。通过问卷调查获取评估诊断性ANCA相关性的数据。实验部分包括检测含ANCA的血清以及针对蛋白酶3的单克隆抗体(MoAb)和中性粒细胞特异性对照MoAb的影响。

结果

在1年的时间里,我们检测了1010份样本,65例患者中发现了ANCA:26例系统性血管炎、12例其他自身免疫性疾病、9例孤立性肾小球肾炎、7例炎症性肠病、6例眼部炎症性疾病以及6例其他疾病。在我们的患者组中,发现小血管血管炎与90%的ANCA阳性相关(韦格纳肉芽肿15/16、变应性肉芽肿性血管炎3/5、显微镜下多血管炎9/9),中血管血管炎为12%(经典结节性多动脉炎1/2、川崎病0/2、过敏性紫癜0/4、大动脉炎1/4)。含ANCA的血清平均抑制杀念珠菌活性65%。与对照MoAb相比,抗蛋白酶MoAb产生抑制作用。

结论

高浓度的c-ANCA对韦格纳肉芽肿的活动形式具有特异性,低滴度的其他类型ANCA对血管炎无诊断价值。ANCA尤其与小血管血管炎相关。已证实ANCA对PMN杀菌活性的抑制可能参与血管炎免疫缺陷的某些临床体征。(表5,参考文献18。)

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