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九种抗抗体检测方法的头对头比较:回顾性评估。

Head-to-Head Comparison of Nine Assays for the Detection of Anti- Antibodies: A Retrospective Evaluation.

机构信息

Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, Medizinische Fakultät, LMU München, Munich, Germany.

Division of Infectious Diseases and Tropical Medicine, University Hospital Ludwig-Maximilian University Munich, Munich, Germany.

出版信息

Ann Lab Med. 2024 Mar 1;44(2):155-163. doi: 10.3343/alm.2023.0212. Epub 2023 Oct 26.

Abstract

BACKGROUND

Echinococcosis is a neglected tropical disease that is severely underdiagnosed in resource-limited settings. In developed countries, diagnosing echinococcosis is challenging, and reliable serological assays are urgently needed. In the Central European Alps, EM is more common than EG; however, data on the diagnostic performance of assays for EM cases are scarce. We evaluated the suitability of nine antibody assays for routine diagnostics.

METHODS

Nine commercially available serological assays for detecting anti- antibodies were compared head-to-head using samples collected from 50 patients with echinococcosis and 50 age- and sex-matched control subjects. The assays are Anti- ELISA (IgG) (Euroimmun), IgG ELISA (DRG), IgG ELISA (IBL International), Western Blot IgG (LDBIO Diagnostics), EUROLINE WB (Euroimmun), Hydatidosis ELISA IgG (VirCell), Hydatidosis VIRCLIA IgG Monotest (VirCell), Ridascreen IgG (R-Biopharm), and Virapid Hydatidosis (VirCell). The cases were ranked according to the WHO-Informal Working Group on Echinococcosis (WHO-IWGE) criteria as confirmed, probable, or possible.

RESULTS

The performance of the assays varied greatly, with overall sensitivities ranging between 50% and 88% and specificities between 62% and 100%. We observed a trend toward better performance with cases classified as "confirmed" using the WHO-IWGE criteria. Combined analysis with sequential screening and confirmatory testing resulted in a maximum sensitivity of 84% and specificity of 100%. Differentiation between EG and EM infections is clinically relevant but was found to be unreliable.

CONCLUSIONS

serological assays are highly variable in terms of sensitivity and specificity. Knowledge of the pre-test probability in the patient cohort is required to choose a suitable assay. A combined approach with screening and confirmatory assays may be the best diagnostic strategy in many situations.

摘要

背景

包虫病是一种被忽视的热带病,在资源有限的环境中严重诊断不足。在发达国家,包虫病的诊断具有挑战性,迫切需要可靠的血清学检测方法。在中欧阿尔卑斯山地区,细粒棘球蚴比多房棘球蚴更常见;然而,针对细粒棘球蚴病例的检测方法的诊断性能数据却很少。我们评估了 9 种抗体检测方法用于常规诊断的适用性。

方法

使用从 50 例包虫病患者和 50 名年龄和性别匹配的对照者中采集的样本,对头对头比较了 9 种市售的用于检测抗-抗体的血清学检测方法。这些检测方法包括:抗-ELISA(IgG)(Euroimmun)、IgG ELISA(DRG)、IgG ELISA(IBL International)、Western Blot IgG(LDBIO Diagnostics)、EUROLINE WB(Euroimmun)、Hydatidosis ELISA IgG(VirCell)、Hydatidosis VIRCLIA IgG Monotest(VirCell)、Ridascreen IgG(R-Biopharm)和 Virapid Hydatidosis(VirCell)。根据世界卫生组织(WHO)非正式棘球蚴病工作组(WHO-IWGE)的标准,病例被分为确诊、可能和疑似。

结果

检测方法的性能差异很大,总体敏感性范围在 50%到 88%之间,特异性在 62%到 100%之间。我们观察到,使用 WHO-IWGE 标准将病例分类为“确诊”时,检测方法的性能有改善的趋势。采用序贯筛查和确认检测的联合分析,可获得 84%的最高敏感性和 100%的特异性。区分细粒棘球蚴和多房棘球蚴感染具有临床意义,但结果不可靠。

结论

血清学检测方法在敏感性和特异性方面差异很大。需要了解患者队列的先验概率,才能选择合适的检测方法。在许多情况下,筛查和确认检测方法的联合应用可能是最佳的诊断策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d58a/10628756/b97b1da74dcb/alm-44-2-155-f1.jpg

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