Loading…

Detection of Antibody to Mycobacterium tuberculosis Protein Antigens in the Cerebrospinal Fluid of Patients with Tuberculous Meningitis

Antibodies against Mycobacterium tuberculosis antigens were detected by enzyme-linked immunosorbent assay in cerebrospinal fluid (CSF) samples obtained from 442 patients with tuberculous meningitis (TBM) and 102 control patients. Antibodies were found in the CSF of 87% of patients with clinical (cul...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of infectious diseases 2002-09, Vol.186 (5), p.678-683
Main Authors: Chandramuki, Akepati, Lyashchenko, Konstantin, Kumari, Haradara Bahubali Veena, Khanna, Neelam, Brusasca, PierNatale, Gourie-Devi, Mandavalli, Satishchandra, Parthasarathy, Shankar, Sursarla Krishna, Ravi, Vasanthapuram, Alcabes, Philip, Kanaujia, Ganga Vishnu, Gennaro, Maria Laura
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Antibodies against Mycobacterium tuberculosis antigens were detected by enzyme-linked immunosorbent assay in cerebrospinal fluid (CSF) samples obtained from 442 patients with tuberculous meningitis (TBM) and 102 control patients. Antibodies were found in the CSF of 87% of patients with clinical (culture-negative) TBM, 72% of patients with culture-positive TBM, and 65% of patients with autopsy-proven TBM. That anti–M. tuberculosis antibodies were detected in the CSF of patients with clinically diagnosed cases more frequently than in patients with culture-positive cases suggests that the detection of antibodies in CSF tends to decrease as bacillary load increases. Of the patients with clinical TBM who were coinfected with human immunodeficiency virus (HIV), 70% exhibited anti–M. tuberculosis antibody in CSF, which suggests that antibody responses in this group were substantially weaker than those in HIV-negative patients with clinical TBM. Some groups showed a stronger response to certain antigens, which suggests that antigen recognition patterns may be specific for the stage of disease
ISSN:0022-1899
1537-6613
DOI:10.1086/342293