Serodiagnosis of Mycobacterium avium-complex pulmonary disease using an enzyme immunoassay kit

被引:87
|
作者
Kitada, Seigo [1 ]
Kobayashi, Kazuo [2 ]
Ichiyama, Satoshi [3 ]
Takakura, Shunij [3 ]
Sakatani, Mitsunori [4 ]
Suzuki, Katsuhiro [4 ]
Takashima, Tetsuya [5 ]
Nagai, Takayuki [5 ]
Sakurabayashi, Ikunosuke [6 ]
Ito, Masami [7 ]
Maekura, Ryoji [1 ]
机构
[1] Natl Hosp Org Natl Toneyama, Dept Internal Med, Toyonaka, Osaka 5608552, Japan
[2] NIAID, Dept Immunol, Tokyo, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Clin Lab Med, Kyoto, Japan
[4] NHO Kinki Chuo Chest Med Ctr, Dept Internal Med, Sakai, Osaka, Japan
[5] Osaka Prefect Med Ctr Resp & Allerg Dis, Dept Med, Habikino Shi, Osaka, Japan
[6] Jich Med Univ, Saitama Med Ctr, Dept Lab Med, Saitama Shi, Japan
[7] Sakamoto Hosp, Dept Internal Med, Toyonaka, Osaka, Japan
关键词
nontuberculous mycobacteria; immunocompetence; sensitivity and specificity;
D O I
10.1164/rccm.200705-771OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale The diagnosis of Mycobacterium avium-complex pulmonary disease (MAC-PD) and/or its discrimination from pulmonary tuberculosis (TB) is sometimes complicated and time consuming. Objectives: We investigated in a six-institution multicenter study whether a serologic test based on an enzyme immunoassay (EIA) kit was useful for diagnosing MAC-PD and for distinguishing it from other lung diseases. Methods: An EIA kit detecting serum IgA antibody to glycopeptido-lipid core antigen specific for MAC was developed. Antibody levels were measured in sera from 70 patients with MAC-PD, 18 with MAC contamination, 37 with pulmonary TB, 45 with other lung diseases, and 76 healthy subjects. Measurements and Main Results: Significantly higher serum IgA antibody levels were detected in patients with MAC-PD than in the other groups (P < 0.0001). Setting the cutoff point at 0.7 U/ml resulted in a sensitivity and specificity of the kit for diagnosing MAC-PD of 843 and 100%, respectively. Significantly higher antibody levels were also found in patients with nodular-bronchiectatic disease compared with fibrocavitary disease in MAC-PD (P < 0.05). There was a positive correlation between the extent of disease on chest computed tomography scans and the levels of antibody (r = 0.43, P < 0.05) in patients with MAC-PD. Conclusions: The EIA kit is useful for the rapid diagnosis of MAC-PD and for differentiating MAC-PD from pulmonary TB and, if validated by studies in other populations, could find wide application in clinical practice.
引用
收藏
页码:793 / 797
页数:5
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