Author:
Kumar Nathella Pavan,Nancy Arul,Viswanathan Vijay,Sivakumar Shanmugam,Thiruvengadam Kannan,Ahamed Shaik Fayaz,Hissar Syed,Kornfeld Hardy,Babu Subash
Abstract
IntroductionChitinase, Indoleamine 2,3-dioxygenesae-1 (IDO-1) and heme oxygenase-1 (HO-1) are candidate diagnostic biomarkers for tuberculosis (TB). Whether these immune markers could also serve as predictive biomarkers of unfavorable treatment outcomes in pulmonary TB (PTB) is not known.MethodsA cohort of newly diagnosed, sputum culture-positive adults with drug-sensitive PTB were recruited. Plasma chitinase protein, IDO protein and HO-1 levels measured before treatment initiation were compared between 68 cases with unfavorable outcomes (treatment failure, death, or recurrence) and 108 control individuals who had recurrence-free cure.ResultsPlasma chitinase and IDO protein levels but not HO-1 levels were lower in cases compared to controls. The low chitinase and IDO protein levels were associated with increased risk of unfavourable outcomes in unadjusted and adjusted analyses. Receiver operating characteristic analysis revealed that chitinase and IDO proteins exhibited high sensitivity and specificity in differentiating cases vs controls as well as in differentiating treatment failure vs controls and recurrence vs controls, respectively. Classification and regression trees (CART) were used to determine threshold values for these two immune markers.DiscussionOur study revealed a plasma chitinase and IDO protein signature that may be used as a tool for predicting adverse treatment outcomes in PTB.
Funder
Department of Biotechnology, Ministry of Science and Technology, India
CRDF Global
Division of Intramural Research, National Institute of Allergy and Infectious Diseases
Subject
Immunology,Immunology and Allergy
Cited by
4 articles.
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