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[利用针对糖肽脂核心抗原的IgA抗体对鸟分枝杆菌复合群进行血清学诊断]

[SERODIAGNOSIS OF THE MYCOBACTERIUM AVIUM COMPLEX BY USING IgA ANTIBODIES FOR THE GLYCOPEPTIDOLIPID CORE ANTIGEN].

作者信息

Higashi Yoshitsugu, Nakamura Shigeki, Tomono Hiromi, Ide Shotaro, Takazono Takahiro, Miyazaki Taiga, Izumikawa Koichi, Yanagihara Katsunori, Yamamoto Yoshihiro, Kohno Shigeru

出版信息

Kekkaku. 2016 Feb;91(2):27-32.

Abstract

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.

摘要

目的

鸟分枝杆菌复合群肺病(MAC - PD)的诊断可能具有挑战性。一种检测血清抗糖脂肽(GPL)核心IgA抗体的血清学诊断酶免疫分析(EIA)试剂盒最近已商业化;然而,其在MAC - PD诊断中的临床实用性仍不明确。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月间在长崎大学医院使用EIA试剂盒进行评估的195例患者进行了回顾性研究。

结果

16例MAC患者中有12例(75.0%)有基础疾病;16例中有8例(50%)有与呼吸系统疾病相关的并发症。确诊为MAC - PD的患者血清阳性和血清阴性背景之间无显著差异。关于血清学诊断EIA试剂盒的准确性,其敏感性和特异性分别为81.3%和88.3%(临界值为0.7 U/ml)。在支气管扩张的假阳性患者中,28.6%对抗MAC治疗有良好反应,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的患者被纳入了假阳性人群。

结论

在本研究中,血清学诊断EIA试剂盒在MAC - PD诊断中显示出良好的敏感性和特异性。需要进一步的临床研究来阐明该试剂盒在明确诊断MAC感染中的作用。

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