Levels of Circulating Immune Complexes Containing Mycobacterium Tuberculosis-specific Antigens in Pulmonary Tuberculosis and Sarcoidosis Patients

• Published in: Indian journal of medical microbiology 2017-04, Vol.35 (2), p.290-292
• Main Authors: Goyal, B., Sheikh, J.A., Agarwal, R., Verma, I.
• Format: Article
• Language: English
• Subjects: Antigen-antibody complexes; Antigens; Biochemistry; Circulating immune complexes; Deoxyribonucleic acid; DNA; Enzyme-linked immunosorbent assay; Filtrate; Health education; Immunoassay; Immunoassays; Immunoglobulins; Laboratories; Mathematical analysis; Patients; Peptides; Proteins; pulmonary tuberculosis; regions of differences antigens; sandwich ELISA; Sarcoidosis; Smear; Studies; Tuberculosis
• ISSN: 0255-0857; 1998-3646
• DOI: 10.4103/0255-0857.209569

The present study was conducted to understand the aetiological link between tuberculosis (TB) and sarcoidosis. Sera from smear-positive TB subjects (n = 24), smear-negative TB subjects (n = 24), sarcoidosis patients (n = 24) and healthy controls (n = 24) were collected and circulating immune complexes were isolated. Sandwich ELISA was performed for detecting four highly specific mycobacterial regions of difference (RD) proteins (early secretory antigenic target 6 [ESAT6], 10 KDa culture filtrate protein [CFP10], 21 KDa CFP [CFP21] and mycobacterial protein from species TB [MPT 64]). Sensitivity and specificity was calculated, and receiver operating characteristic plots were plotted. Non-parametric Mann–Whitney U-test was used to calculate statistical significance. Seventy per cent of sarcoidosis patients showed the presence of immune complexes of mycobacterial RD proteins similar to that observed in the sera of smear-negative TB patients as opposed to antibody-based detection assay based on these RD proteins. Thus, immunoassays based on specific mycobacterial RD proteins also need to be developed and validated carefully to differentiate TB and sarcoidosis, a close mimic of smear-negative tuberculosis.