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Clinical and Diagnostic Laboratory Immunology, January 2005, p. 44-51, Vol. 12, No. 1
1071-412X/05/$08.00+0 doi:10.1128/CDLI.12.1.44-51.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Department of Host Defense, Osaka City University Graduate School of Medicine, Abeno-ku,1 Toneyama Institute for Tuberculosis Research, Toyonaka-shi,3 Department of Internal Medicine, Toneyama National Hospital, Toyonaka-shi, Osaka,2 Japan BCG Laboratory, Kiyose-shi, Tokyo, Japan4
Received 6 February 2004/ Returned for modification 20 May 2004/ Accepted 6 October 2004
We report the development of a serodiagnostic method for Mycobacterium avium complex (MAC) disease with an enzyme immunoassay (EIA) with the MAC-specific glycopeptidolipid (GPL) core as the antigen. In this study, we confirmed by EIA that the GPL core antibody was in the sera of immunocompetent patients with MAC disease. The EIA for quantifying the GPL core antibody was evaluated as a clinical tool for serodiagnosis of pulmonary MAC disease. A significant increase in GPL core antibodies (immunoglobulins G, A, and M) was detected in sera of patients with MAC pulmonary diseases when they were compared to patients who were colonized with MAC, patients with Mycobacterium kansasii disease or tuberculosis, and healthy subjects. The sensitivities and specificities of the GPL core-based EIA for diagnosis of MAC pulmonary disease were 72.6% and 92.2%, respectively, for IgG, 92.5% and 95.1%, respectively, for IgA, and 78.3% and 91.0%, respectively, for IgM. The best sensitivity and specificity were obtained by measuring immunoglobulin A antibodies against GPL core antigen. The level of GPL core antibodies reflected disease activity, since it decreased in cured MAC patients who had responded to chemotherapy. Measurement of serum antibodies against GPL core is useful for both diagnosis and assessment of disease activity in MAC disease of the lung.
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