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大样本抗核抗体检测中 HEp-2 间接免疫荧光法的复杂模式。

Complex patterns on HEp-2 indirect immunofluorescence assay in a large sample referred for anti-cell autoantibodies detection.

机构信息

Immunology Division, Sabin Medicina and Health, Brasília, Brazil.

Long-term Care Unit, Hospital Geral de Fortaleza, Fortaleza, Ceará, Brazil.

出版信息

Front Immunol. 2024 Jan 12;14:1256526. doi: 10.3389/fimmu.2023.1256526. eCollection 2023.

DOI:10.3389/fimmu.2023.1256526
PMID:38283335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10811459/
Abstract

INTRODUCTION

The combination of patterns is a frequent and challenging situation in the daily laboratory routine of autoantibodies testing using HEp-2 cells indirect immunofluorescence assay (HEp-2-IFA). Recently, the Brazilian Consensus on Autoantibodies (BCA) named these combinations as complex patterns (CPs) and organized them into 3 subtypes: multiple, mixed, and composite. This study aimed to describe the most frequent combinations of HEp-2-IIF patterns according to this new nomenclature.

METHODS

Routine HEp-2-IFA results reported in January and June 2017 were reviewed using the new BCA classification. Visual pattern recognition was performed by experts on HEp-2-IFA readings, using the International Consensus on Antinuclear Antibodies (ANA) Patterns (ICAP) and BCA recommendations.

RESULTS

54,990 serum samples from different patients were tested for ANA-HEp-2, and 11,478 (20.9%) were positive at a titer ≥ 1/80. Among these positive samples, 1,111 (9.7%) displayed CPs, divided into 95 different combinations. A higher proportion of CPs was observed in the pediatric age group. Multiple, mixed, and composite patterns were present in 85.3, 5.4, and 9.5% of the samples, respectively. In the multiple/mixed pattern group (n=1,005), double, triple, and quadruple combinations (ICAP/BCA codes) were observed in 97.7%, 2.2%, and 0.1%, respectively. The double nuclear pattern was the most prevalent combination observed (67.6%). The most common CPs registered were AC-4 (nuclear fine speckled) + AC-6,7 (nuclear discrete dots) (n=264); AC-2 (nuclear dense fine speckled) + AC-6,7 (n=201); AC-4+AC-8,9,10 (nucleolar) (n=129); and AC-3 (centromere)+AC-4 (n=124). All of these combinations were in the multiple subgroup.

CONCLUSION

Almost 10% of positive results in the HEp-2 procedure displayed CPs. Among the 3 subtypes of CPs proposed, the multiple pattern was the most prevalent, especially in the pediatric population. The AC-4, AC-2, and AC-6,7 were the most prevalent single patterns observed in the combinations described in this study. There was a significant association between age and the prevalence of most combined patterns. The AC-4+AC-6,7 combination was the most prevalent complex pattern detected regardless of the age group. The AC-2+AC-6,7 was more prevalent in younger individuals. The concepts involved in the CPs definition should add value to the reading and interpretation of the HEp-2-IIF assay.

摘要

简介

在使用 HEp-2 细胞间接免疫荧光法(HEp-2-IFA)进行自身抗体检测的日常实验室工作中,模式组合是一种常见且具有挑战性的情况。最近,巴西自身抗体共识(BCA)将这些组合命名为复杂模式(CPs),并将它们分为 3 个亚型:多重、混合和复合。本研究旨在根据这一新命名法描述 HEp-2-IIF 模式中最常见的组合。

方法

使用新的 BCA 分类回顾了 2017 年 1 月和 6 月报告的常规 HEp-2-IFA 结果。专家使用国际核抗体共识(ANA)模式(ICAP)和 BCA 建议对 HEp-2-IFA 读数进行视觉模式识别。

结果

对来自不同患者的 54,990 份血清样本进行了抗核抗体-HEp-2 检测,11,478 份(20.9%)滴度≥1/80 为阳性。在这些阳性样本中,有 1,111 份(9.7%)显示 CPs,分为 95 种不同的组合。在儿科年龄组中观察到更高比例的 CPs。多、混和复合模式分别占样本的 85.3%、5.4%和 9.5%。在多/混模式组(n=1,005)中,双、三、四重组合(ICAP/BCA 码)分别观察到 97.7%、2.2%和 0.1%。最常见的组合是双核模式(67.6%)。登记的最常见 CPs 是 AC-4(核细点状)+AC-6,7(核离散点)(n=264);AC-2(核密集细点状)+AC-6,7(n=201);AC-4+AC-8,9,10(核仁)(n=129);和 AC-3(着丝粒)+AC-4(n=124)。所有这些组合都属于多亚组。

结论

HEp-2 程序中近 10%的阳性结果显示 CPs。在所提出的 3 种 CPs 亚型中,多重模式最为常见,尤其是在儿科人群中。在本研究中描述的组合中,最常见的单一模式是 AC-4、AC-2 和 AC-6,7。年龄与大多数联合模式的流行率之间存在显著关联。无论年龄组如何,AC-4+AC-6,7 复合模式都是最常见的复杂模式。CPs 定义中涉及的概念应该为 HEp-2-IIF 检测的阅读和解释增加价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/2b8b192116c1/fimmu-14-1256526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/7949f5c2d92f/fimmu-14-1256526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/34ed715b6f0d/fimmu-14-1256526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/86397e4dac2f/fimmu-14-1256526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/2b8b192116c1/fimmu-14-1256526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/7949f5c2d92f/fimmu-14-1256526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/34ed715b6f0d/fimmu-14-1256526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/86397e4dac2f/fimmu-14-1256526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54e1/10811459/2b8b192116c1/fimmu-14-1256526-g004.jpg

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