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单一细菌分离加抗 GPL-Core IgA 抗体诊断非结核分枝杆菌肺病。

The Diagnosis of Nontuberculous Mycobacterial Pulmonary Disease by Single Bacterial Isolation Plus Anti-GPL-Core IgA Antibody.

机构信息

National Hospital Organization Osaka Toneyama Medical Center, Toyonaka, Osaka, Japan.

Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

出版信息

Microbiol Spectr. 2022 Feb 23;10(1):e0140621. doi: 10.1128/spectrum.01406-21. Epub 2022 Jan 5.

Abstract

Although serum anti-glycopeptidolipid (GPL)-core IgA antibody is a highly specific test for infection with Mycobacterium avium complex (MAC), Mycobacterium abscessus, and its subspecies , subsp. , and subsp. (MAB), its use for the definitive diagnosis of MAC pulmonary disease (PD) and MAB-PD are unknown. To clarify the diagnostic accuracy of the anti-GPL-core IgA antibody test among patients with radiologically suspected MAC-PD or MAB-PD who already have a single positive sputum culture test. The first isolations of MAC and MAB from patients with radiologically suspected MAC-PD or MAB-PD at the Osaka Toneyama Medical Center between January 2006 and December 2020 were collected. Patients were enrolled when their serum anti-GPL-core IgA antibody was measured during the 3 months before and after the first isolation. We retrospectively compared the results of anti-GPL-core IgA antibody testing with the final diagnoses based on the current guidelines. We included 976 patients for analysis. The serum anti-GPL-core IgA antibody was positive in 699 patients (71.6%). The positive predictive value of anti-GPL-core IgA antibody for the diagnosis of MAC-PD or MAB-PD was 97.4%. The median time required for the second positive culture after the first isolation was 51 days (interquartile range 12 to 196 days). The positive serum anti-GPL-core IgA antibody test allowed an early and definitive diagnosis of MAC-PD or MAB-PD in those who already had a single positive sputum culture test. To satisfy the microbiologic criteria of the current diagnostic guideline for nontuberculous mycobacterial pulmonary disease (PD), at least two positive sputum cultures of the same species of mycobacteria from sputum are required to avoid the casual isolation of mycobacteria. This study showed that the positivity of a serum anti-glycopeptidolipid (GPL)-core IgA antibody test has an excellent diagnostic ability among patients with radiologically suspected Mycobacterium avium complex (MAC)-PD or Mycobacterium abscessus (MAB)-PD who already had a single positive sputum culture test. The usage of single culture isolation plus anti-GPL-core IgA antibody as another diagnostic criterion has a time, cost, and effort-saving effect. Furthermore, it will facilitate the diagnosis of MAC-PD or MAB-PD in the early stage of disease because serum anti-GPL-core IgA antibody becomes high in these patients. Therefore, we proposed adding single culture isolation plus anti-GPL-core IgA antibody as "combined microbiological and serological criteria" to the diagnostic guidelines for MAC-PD and MAB-PD.

摘要

虽然血清抗糖肽脂(GPL)核心 IgA 抗体是感染鸟分枝杆菌复合群(MAC)、脓肿分枝杆菌及其亚种、亚种和亚种(MAB)的高度特异性试验,但它在 MAC 肺疾病(PD)和 MAB-PD 的明确诊断中的用途尚不清楚。为了阐明在已经有单一阳性痰培养试验的影像学疑似 MAC-PD 或 MAB-PD 患者中,抗-GPL 核心 IgA 抗体试验的诊断准确性。收集了 2006 年 1 月至 2020 年 12 月期间大阪豊中医疗中心影像学疑似 MAC-PD 或 MAB-PD 患者的首次分离物 MAC 和 MAB。当患者在首次分离后的 3 个月内测量血清抗-GPL 核心 IgA 抗体时,他们被纳入研究。我们回顾性地将抗-GPL 核心 IgA 抗体检测结果与现行指南的最终诊断进行比较。我们对 976 名患者进行了分析。699 名患者(71.6%)的血清抗-GPL 核心 IgA 抗体呈阳性。抗-GPL 核心 IgA 抗体对 MAC-PD 或 MAB-PD 的诊断阳性预测值为 97.4%。首次分离后第二次阳性培养的中位时间为 51 天(四分位距 12 至 196 天)。阳性血清抗-GPL 核心 IgA 抗体试验允许在已经有单一阳性痰培养试验的情况下,对 MAC-PD 或 MAB-PD 进行早期和明确的诊断。为了满足非结核分枝杆菌肺病(PD)现行诊断指南的微生物学标准,需要从痰中至少分离出两种相同种属分枝杆菌的阳性痰培养物,以避免分枝杆菌的偶然分离。这项研究表明,在已经有单一阳性痰培养试验的影像学疑似鸟分枝杆菌复合群(MAC)-PD 或脓肿分枝杆菌(MAB)-PD 患者中,血清抗糖肽脂(GPL)核心 IgA 抗体试验具有极好的诊断能力。使用单一培养分离加抗-GPL 核心 IgA 抗体作为另一种诊断标准具有节省时间、成本和精力的效果。此外,由于这些患者的血清抗-GPL 核心 IgA 抗体水平升高,因此将有助于疾病早期诊断 MAC-PD 或 MAB-PD。因此,我们建议将单一培养分离加抗-GPL 核心 IgA 抗体作为“组合微生物学和血清学标准”添加到 MAC-PD 和 MAB-PD 的诊断指南中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7736/8729764/08522f58d0c6/spectrum.01406-21-f001.jpg

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