TY - JOUR
T1 - Clinical evaluation of a blood assay to diagnose paucibacillary tuberculosis via bacterial antigens
AU - Liu, Chang
AU - Lyon, Christopher J.
AU - Bu, Yang
AU - Deng, Zaian
AU - Walters, Elisabetta
AU - Li, Yan
AU - Zhang, Liqun
AU - Hesseling, Anneke C.
AU - Graviss, Edward A.
AU - Hu, Ye
N1 - Funding Information:
Employment or Leadership: C. Liu, Arizona State University; Y. Hu, Arizona State University, Houston Methodist Research Institute. Consultant or Advisory Role: None declared. Stock Ownership: None declared. Honoraria: None declared. Research Funding: Y. Hu, Arizona State University. Support for the performance of this study was provided by the US National Institute of Allergy and Infectious Diseases grants R01 Al113725-01A1 and R01 AI122932-01A1, and the US Eunice Kennedy Shriver National Institute of Child Health & Human Development grant R01 HD090927-01A1. Expert Testimony: None declared. Patents: None declared.
Publisher Copyright:
© 2017 American Association for Clinical Chemistry.
PY - 2018/5
Y1 - 2018/5
N2 - BACKGROUND: The diagnosis of active tuberculosis (TB) cases primarily relies on methods that detect Mycobacterium tuberculosis (Mtb) bacilli or their DNA in patient samples (e.g., mycobacterial culture and Xpert MTB/RIF assays), but these tests have low clinical sensitivity for patients with paucibacillary TB disease. Our goal was to evaluate the clinical performance of a newly developed assay that can rapidly diagnose active TB cases by direct detection of Mtb-derived antigens in patients’ blood samples. METHODS: Nanoparticle (NanoDisk)-enriched peptides derived from the Mtb virulence factors CFP-10 (10-kDa culture factor protein) and ESAT-6 (6-kDa early secretory antigenic target) were analyzed by high-throughput mass spectrometry (MS). Serum from 294 prospectively enrolled Chinese adults were analyzed with this NanoDisk-MS method to evaluate the performance of direct serum Mtbantigen measurement as a means for rapid diagnosis of active TB cases. RESULTS: NanoDisk-MS diagnosed 174 (88.3%) of the study’s TB cases, with 95.8% clinical specificity, and with 91.6% and 85.3% clinical sensitivity for culture-positive and culture-negative TB cases, respectively. NanoDisk-MS also exhibited 88% clinical sensitivity for pulmonary and 90% for extrapulmonary TB, exceeding the diagnostic performance of mycobacterial culture for these cases. CONCLUSIONS: Direct detection and quantification of serum Mtb antigens by NanoDisk-MS can rapidly and accurately diagnose active TB in adults, independent of disease site or culture status, and outperform Mycobacterium-based TB diagnostics.
AB - BACKGROUND: The diagnosis of active tuberculosis (TB) cases primarily relies on methods that detect Mycobacterium tuberculosis (Mtb) bacilli or their DNA in patient samples (e.g., mycobacterial culture and Xpert MTB/RIF assays), but these tests have low clinical sensitivity for patients with paucibacillary TB disease. Our goal was to evaluate the clinical performance of a newly developed assay that can rapidly diagnose active TB cases by direct detection of Mtb-derived antigens in patients’ blood samples. METHODS: Nanoparticle (NanoDisk)-enriched peptides derived from the Mtb virulence factors CFP-10 (10-kDa culture factor protein) and ESAT-6 (6-kDa early secretory antigenic target) were analyzed by high-throughput mass spectrometry (MS). Serum from 294 prospectively enrolled Chinese adults were analyzed with this NanoDisk-MS method to evaluate the performance of direct serum Mtbantigen measurement as a means for rapid diagnosis of active TB cases. RESULTS: NanoDisk-MS diagnosed 174 (88.3%) of the study’s TB cases, with 95.8% clinical specificity, and with 91.6% and 85.3% clinical sensitivity for culture-positive and culture-negative TB cases, respectively. NanoDisk-MS also exhibited 88% clinical sensitivity for pulmonary and 90% for extrapulmonary TB, exceeding the diagnostic performance of mycobacterial culture for these cases. CONCLUSIONS: Direct detection and quantification of serum Mtb antigens by NanoDisk-MS can rapidly and accurately diagnose active TB in adults, independent of disease site or culture status, and outperform Mycobacterium-based TB diagnostics.
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U2 - 10.1373/clinchem.2017.273698
DO - 10.1373/clinchem.2017.273698
M3 - Article
C2 - 29348166
AN - SCOPUS:85046143822
SN - 0009-9147
VL - 64
SP - 791
EP - 800
JO - Clinical Chemistry
JF - Clinical Chemistry
IS - 5
ER -