Tuberc Respir Dis > Volume 45(2); 1998 > Article
Tuberculosis and Respiratory Diseases 1998;45(2):271-279.
DOI: https://doi.org/10.4046/trd.1998.45.2.271    Published online April 1, 1998.
Diagnostic Significance of the Serologic Test Using Antigen of Mycobacterium Tuberculosis for Antibody Detection by ELISA.
Jae Min Park, Yeon Soo Park, Yeon Soo Chang, Young Sam Kim, Kang Hyun Ahn, Se Kyu Kim, Joon Chang, Sung Kyu Kim, Won Young Lee, Shang Rae Cho
1Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
2Institute of Chest Diseases, Yonsei University College of Medicine, Seoul, Korea.
3Department of Microbiology, Yonsei University College of Medicine, Seoul, Korea.
Abstract
BACKGROUND
Diagnosis by direct microscopy and/or by culture of the Mycobacterium tuberculosis from body fluids or biopsy specimens is "Gold standard". However, the sensitivity of direct microscopy after Ziehl-Neelsen staining is relatively low and culture of mycobacteria is time consuming. Detection of mycobacterial DNA in clinical samples by the polymerase chain reaction is highly sensitive but laborious and expensive. Therefore, rapid, sensitive and readily applicable new tests need to be developed. So we had evaluated the clinical significance of serologic detection of antibody to 38 kDa antigen, which is known as the most specific to the M. tuberculosis complex, and culture filtrate antigen by ELISA in sputum AFB smear negative patients. METHOD: In this study, culture tests for acid fast bacilli with sputa or bronchial washing fluids of 183 consecutive patients who were negative of sputum AFB smear were performed. Simultaneously serum antibodies to 38 kDa antigen and unheated culture filtrate of M. tuberculosis were detected by an ELISA method. RESULTS: The optical densities of ELISA test with 38 kDa and culture filtrate antigen were significantly higher in active pulmonary tuberculosis cases than in non tuberculous pulmonary diseases (p<0.05), but in patients with active pulmonary tuberculosis, those of the sputum culture positive patients for M. tuberculosis were not significantly different from those of the sputum culture negative cases(p>O.05). In the smear-negative active pulmonary tuberculosis patients, the sensitivity of the ELISA using 38 kDa antigen and culture filtrate was 20.0% and 31.4%, respectively. The specificity was 95.3% and 93.9%, respectively. CONCLUSION: In active pulmonary tuberculosis but smear negative, the serologic detection of antibody to 38 kDa antigen and culture filtrate by ELISA cannot substitute traditional diagnostic tests and does not have clinically significant role to differenciate the patient with active pulmonary tuberculosis from other with non-tuberculous pulmonary diseases.
Key Words: Active pulmonary tuberculosis, Serologic detection of antibody, 38 kDa antigen, Culture filtrate


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