用糖肽类核心抗原的IgA抗体进行禽分枝杆菌复合体的血清诊断。

Kekkaku : [Tuberculosis] Pub Date : 2016-02-01
Yoshitsugu Higashi, Shigeki Nakamura, Hiromi Tomono, Shotaro Ide, Takahiro Takazono, Taiga Miyazaki, Koichi Izumikawa, Katsunori Yanagihara, Yoshihiro Yamamoto, Shigeru Kohno
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引用次数: 0

摘要

目的:鸟分枝杆菌复合肺部疾病(MAC-PD)的诊断具有挑战性。一种检测血清抗糖肽类脂(GPL)核心IgA抗体的血清诊断酶免疫测定(EIA)试剂盒最近已商品化;然而,其在MAC-PD诊断中的临床应用尚不清楚。本研究旨在评估该试剂盒的可用性,并确定影响检测准确性的因素。方法:我们对2012年11月至2014年3月期间在长崎大学医院用EIA试剂盒进行评估的195例患者进行回顾性研究。结果:16例MAC患者中有12例(75.0%)存在基础疾病;16例患者中有8例(50%)有与呼吸道疾病相关的并发症。确诊MAC-PD患者的血清阳性和血清阴性背景无显著差异。在准确性方面,血清诊断EIA试剂盒的敏感性为81.3%,特异性为88.3%(临界值为0.7 U/ml)。在假阳性的支气管扩张患者中,28.6%的患者对抗mac治疗反应良好,这表明EIA试剂盒的敏感性可能高于基于培养的诊断,因为临床诊断为MAC-PD的患者也包括在假阳性人群中。结论:在本研究中,血清诊断EIA试剂盒对MAC-PD的诊断具有良好的敏感性和特异性。需要进一步的临床研究来明确该试剂盒在明确诊断MAC感染中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[SERODIAGNOSIS OF THE MYCOBACTERIUM AVIUM COMPLEX BY USING IgA ANTIBODIES FOR THE GLYCOPEPTIDOLIPID CORE ANTIGEN].

Purpose: The diagnosis of Mycobacterium avium complex pulmonary disease (MAC-PD) can be challenging. A serodiagnosis enzyme immunoassay (EIA) kit, which detects the serum anti-glycopeptidolipid (GPL) core IgA antibody, has been commercialized recently; however, its clinical usefulness in the diagnosis of MAC-PD is still unclear. This study aimed to evaluate the availability of this kit and identify factors affecting testing accuracy.

Methods: We performed a retrospective study of 195 patients who were evaluated with an EIA kit at Nagasaki University Hospital between November 2012 and March 2014.

Results: 12 of 16 (75.0%) MAC patients have underlying diseases ; 8 of 16 (50%) had complications associated with respiratory diseases. There were no significant differences between the seropositive and seronegative background of patients with confirmed MAC-PD. Regarding the accuracy of serodiagnosis EIA kit, its sensitivity and specificity were 81.3% and 88.3% (with a cut-off value of 0.7 U/ml), respectively. Of false-positive patients with bronchiectasis, 28.6 % demonstrated a good response to anti-MAC treatment, indicating that the sensitivity of the EIA kit might be higher than that of culture-based diagnosis because patients with clinically diagnosed MAC-PD were included in the false-positive population.

Conclusions: In the current study, the serodiagnosis EIA kit demonstrated good sensitivity and specificity for the diagnosis of MAC-PD. Further clinical investigations are necessary to clarify the role of this kit in definitively diagnosing MAC infections.

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