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Journal of Clinical Microbiology, June 2000, p. 2227-2231, Vol. 38, No. 6
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
A Comparison of Seven Tests for Serological Diagnosis
of Tuberculosis
Sudha
Pottumarthy,
Virginia
C.
Wells, and
Arthur J.
Morris*
Department of Microbiology, Green Lane and
National Women's Hospitals, Auckland, New Zealand
Received 23 September 1999/Returned for modification 19 November
1999/Accepted 29 February 2000
Seven serological tests, two immunochromatographic tests, ICT
Tuberculosis and RAPID TEST TB, and five enzyme-linked
immunosorbent assays, TUBERCULOSIS IgA EIA, PATHOZYME-TB complex,
PATHOZYME-MYCO IgG, PATHOZYME-MYCO IgA, and PATHOZYME-MYCO IgM,
were evaluated simultaneously with 298 serum samples from three groups
of individuals: 44 patients with active tuberculosis, 204 controls who
had undergone the Mantoux test (89 Mantoux test-positive and 115 Mantoux test-negative controls), and 50 anonymous controls. The
sensitivities of the tests with sera from patients with active
tuberculosis were poor to modest, ranging from 16 to 57%. All the
tests performed equally with sera from subgroups of those with active
tuberculosis, those with pulmonary (33 patients) versus extrapulmonary
(11 patients) disease, and those who were smear positive (24 patients)
versus smear negative (12 patients) (P > 0.05). The
specificities of the tests ranged from 80 to 97% with sera from the
Mantoux test controls and 62 to 100% with sera from the anonymous
controls. The TUBERCULOSIS IgA EIA had the highest sensitivity (57%)
with sera from patients with active tuberculosis, with a high
specificity of 93% with sera from the Mantoux test controls, but a
very poor specificity of 62% with sera from the anonymous controls.
Overall, ICT Tuberculosis followed by PATHOZYME-MYCO IgG had the best
performance characteristics, with sensitivities of 41 and 55%,
respectively, with sera from patients with active tuberculosis and
specificities of 96 and 89%, respectively, with sera from the Mantoux
test controls and 88 and 90%, respectively, with sera from the
anonymous controls. By combining all the test results, a maximum
sensitivity of 84% was obtained, with reciprocal drops in
specificities to 55 and 42% for the Mantoux test controls and
anonymous controls, respectively. The best combination was that of ICT
Tuberculosis and PATHOZYME-MYCO IgG, with a sensitivity of 66% and a
specificity of 86% for the Mantoux test controls and a sensitivity and
specificity of 78% for the anonymous controls. While a negative result
by any one of these tests would be useful in helping to exclude disease
in a population with a low prevalence of tuberculosis, a positive result may aid in clinical decision making when applied to symptomatic patients being evaluated for active tuberculosis.
*
Corresponding author. Mailing address: Microbiology
Laboratory, Green Lane Hospital, Green Lane West, Auckland 1003, New
Zealand. Phone: (649) 630-9943 ext. 3935. Fax: (649) 630-9785. E-mail: arthurm{at}ahsl.co.nz.
Journal of Clinical Microbiology, June 2000, p. 2227-2231, Vol. 38, No. 6
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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