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抗中性粒细胞胞浆抗体及其临床意义。

Anti-neutrophil cytoplasmic antibodies and their clinical significance.

机构信息

Center of Excellence in Immunology and Immune-mediated diseases, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Division of Pediatric Nephrology, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Clin Rheumatol. 2018 Apr;37(4):875-884. doi: 10.1007/s10067-018-4062-x. Epub 2018 Mar 10.

DOI:10.1007/s10067-018-4062-x
PMID:29525845
Abstract

Anti-neutrophil cytoplasmic antibodies (ANCA) are a group of autoantibodies that cause systemic vascular inflammation by binding to target antigens of neutrophils. These autoantibodies can be found in serum from patients with systemic small-vessel vasculitis and they are considered as a biomarker for ANCA-associated vasculitis (AAV). A conventional screening test to detect ANCA in the serum is indirect immunofluorescence study, and subsequently confirmed by enzyme-linked immunosorbent assay. A positive staining of ANCA can be classified into three main categories based on the staining patterns: cytoplasmic, perinuclear, and atypical. Patients with granulomatosis with polyangiitis (GPA) mostly have a positive cytoplasmic staining pattern (c-ANCA) whilst a perinuclear pattern (p-ANCA) is more common in microscopic polyangiitis (MPA) and eosinophilic granulomatosis with polyangiitis (EGPA) patients. Atypical pattern (a-ANCA) is rarely seen in patients with systemic small-vessel vasculitis but it can be found in other conditions. Here, techniques for ANCA detection, ANCA staining patterns and their clinical significances are reviewed.

摘要

抗中性粒细胞胞浆抗体 (ANCA) 是一组自身抗体,通过与中性粒细胞的靶抗原结合引起系统性血管炎症。这些自身抗体可在系统性小血管血管炎患者的血清中检出,被认为是 ANCA 相关性血管炎 (AAV) 的生物标志物。检测血清中 ANCA 的常规筛选试验是间接免疫荧光研究,随后通过酶联免疫吸附试验进行确认。根据染色模式,ANCA 的阳性染色可分为三种主要类型:细胞质型、核周型和非典型型。肉芽肿性多血管炎 (GPA) 患者大多呈阳性细胞质染色模式 (c-ANCA),而显微镜下多血管炎 (MPA) 和嗜酸性肉芽肿性多血管炎 (EGPA) 患者则更常见核周型 (p-ANCA)。非典型型 (a-ANCA) 在系统性小血管血管炎患者中很少见,但也可见于其他疾病。本文综述了 ANCA 的检测技术、染色模式及其临床意义。

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本文引用的文献

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Position paper: Revised 2017 international consensus on testing of ANCAs in granulomatosis with polyangiitis and microscopic polyangiitis.立场文件:2017 年关于肉芽肿性多血管炎和显微镜下多血管炎抗中性粒细胞胞浆抗体检测的国际共识修订版。
Nat Rev Rheumatol. 2017 Nov;13(11):683-692. doi: 10.1038/nrrheum.2017.140. Epub 2017 Sep 14.
2
ANCA-Associated Vasculitis: Pathogenesis, Models, and Preclinical Testing.抗中性粒细胞胞质抗体相关性血管炎:发病机制、模型和临床前检测。
Semin Nephrol. 2017 Sep;37(5):418-435. doi: 10.1016/j.semnephrol.2017.05.016.
3
Prospective monitoring of in vitro produced PR3-ANCA does not improve relapse prediction in granulomatosis with polyangiitis.
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Biomolecules. 2024 Aug 25;14(9):1054. doi: 10.3390/biom14091054.
4
Three cases of relapsed eosinophilic sinusitis without eosinophilia during mepolizumab maintenance therapy for eosinophilic granulomatosis with polyangiitis.例三为嗜酸性粒细胞性肉芽肿伴多血管炎患者在美泊利单抗维持治疗期间出现复发性无嗜酸性粒细胞性鼻旁窦炎。
Clin Rheumatol. 2024 Nov;43(11):3577-3580. doi: 10.1007/s10067-024-07133-w. Epub 2024 Sep 9.
5
The value of the current histological scores and classifications of ANCA glomerulonephritis in predicting long-term outcome.抗中性粒细胞胞浆抗体相关性肾小球肾炎当前的组织学评分及分类在预测长期预后方面的价值。
Clin Kidney J. 2024 May 6;17(7):sfae125. doi: 10.1093/ckj/sfae125. eCollection 2024 Jul.
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Ren Fail. 2024 Dec;46(2):2357743. doi: 10.1080/0886022X.2024.2357743. Epub 2024 Jun 7.
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Clinical and prognostic features of Korean patients with MPO-ANCA, PR3-ANCA and ANCA-negative vasculitis.韩国MPO-ANCA、PR3-ANCA及ANCA阴性血管炎患者的临床和预后特征
Clin Exp Rheumatol. 2017 Mar-Apr;35 Suppl 103(1):111-118. Epub 2017 Mar 23.
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Predictors of Poor Outcome in ANCA-Associated Vasculitis (AAV).抗中性粒细胞胞浆抗体相关性血管炎(AAV)不良预后的预测因素。
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Medicine (Baltimore). 2016 Oct;95(40):e5096. doi: 10.1097/MD.0000000000005096.