Affiliation:
1. Departments of Medicine
2. Biochemistry
3. Microbiology & Immunology, Albert Einstein College of Medicine, Bronx, New York
4. Pathology
Abstract
ABSTRACT
The immunodominance of
Mycobacterium tuberculosis
proteins malate synthase (MS) and MPT51 has been demonstrated in case-control studies with patients from countries in which tuberculosis (TB) is endemic. The value of these antigens for the serodiagnosis of TB now is evaluated in a cross-sectional study of pulmonary TB suspects in the United States diagnosed to have TB, HIV-associated TB, or other respiratory diseases (ORD). Serum antibody reactivity to recombinant purified MS and MPT51 was determined by enzyme-linked immunosorbent assays (ELISAs) of samples from TB suspects and well-characterized control groups. TB suspects were diagnosed with TB (
n
= 87; 49% sputum microscopy negative, 20% HIV
+
) or ORD (
n
= 63; 58% HIV
+
). Antibody reactivity to MS and MPT51 was significantly higher in U.S. HIV
+
/TB samples than in HIV
−
/TB samples (
P
< 0.001), and it was significantly higher in both TB groups than in control groups with latent TB infection (
P
< 0.001). Antibody reactivity to both antigens was higher in U.S. HIV
+
/TB samples than in HIV
+
/ORD samples (
P
= 0.052 for MS,
P
= 0.001 for MPT51) but not significantly different between HIV
−
/TB and HIV
−
/ORD. Among U.S. HIV
+
TB suspects, a positive anti-MPT51 antibody response was strongly and significantly associated with TB (odds ratio, 11.0; 95% confidence interval, 2.3 to 51.2;
P
= 0.002). These findings have implications for the adjunctive use of TB serodiagnosis with these antigens in HIV
+
subjects.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
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