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Field evaluation of a blood based test for active tuberculosis in endemic settings
Author(s) -
Aasia Khaliq,
Resmi Ravindran,
Syed Fahadulla Hussainy,
Viwanathan V. Krishnan,
Atiqa Ambreen,
Noshin Wasim Yusuf,
Shagufta Irum,
H.A. Abdul-Rashid,
Muhammad Jamil,
Fareed Zaffar,
Muhammad Nawaz Chaudhry,
Puneet Kumar Gupta,
Muhammad Akhtar,
Imran Khan
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0173359
Subject(s) - medicine , sputum , lipoarabinomannan , tuberculosis , multiplex , serology , mycobacterium tuberculosis , population , immunology , intensive care medicine , virology , antibody , environmental health , pathology , bioinformatics , biology
Over 9 million new active tuberculosis (TB) cases emerge each year from an enormous pool of 2 billion individuals latently infected with Mycobacterium tuberculosis ( M . tb .) worldwide. About 3 million new TB cases per year are unaccounted for, and 1.5 million die. TB, however, is generally curable if diagnosed correctly and in a timely manner. The current diagnostic methods for TB, including state-of-the-art molecular tests, have failed in delivering the capacity needed in endemic countries to curtail this ongoing pandemic. Efficient, cost effective and scalable diagnostic approaches are critically needed. We report a multiplex TB serology panel using microbead suspension array containing a combination of 11 M . tb . antigens that demonstrated overall sensitivity of 91% in serum/plasma samples from TB patients confirmed by culture. Group wise sensitivities for sputum smear positive and negative patients were 95%, and 88%, respectively. Specificity of the test was 96% in untreated COPD patients and 91% in general healthy population. The sensitivity of this test is superior to that of the frontline sputum smear test with a comparable specificity (30–70%, and 93–99%, respectively). The multiplex serology test can be performed with scalability from 1 to 360 patients per day, and is amenable to automation for higher (1000s per day) throughput, thus enabling a scalable clinical work flow model for TB endemic countries. Taken together, the above results suggest that well defined antibody profiles in blood, analyzed by an appropriate technology platform, offer a valuable approach to TB diagnostics in endemic countries.

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