کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6087019 | 1589427 | 2016 | 11 صفحه PDF | دانلود رایگان |
- PBMC's transcriptional profiles are distinct in tuberculosis associated or not with NIDDM
- NCF1 and ORM discriminate TBP from LTBI and non-infected in general population
- FPR2 transcriptional levels discriminate TBP from LTBI and non-infected in NIDDM
- NCF1, ORM and FPR2 are potential diagnostic biomarkers for PTB
Our objective was to identify transcriptional biomarkers in peripheral blood mononuclear cells (PBMC) that discriminate individuals with latent tuberculosis infection (LTBI) from those with pulmonary tuberculosis (PTB) in subjects with non-insulin-dependent diabetes mellitus (NIDDM) and in individuals without NIDDM. Using gene expression microarrays we identified differentially expressed genes from lungs of mice infected with Mycobacterium tuberculosis (Mtb) or a mutant (ÎsigH) representing a non-inflammatory model. Genes expressed in blood, with inflammatory related functions were evaluated in humans by RT-qPCR. NCF1 and ORM transcripts have the better discriminatory capacity to identify PTB subjects from LTBI and non-infected controls (NICs) independently of the presence of NIDDM. The sequential evaluation of the mRNA levels of NCF1 and ORM as multiple diagnostic tests showed 95% Sensitivity (Se) and 80% Specificity (Sp). In addition, FPR2 promises to be a good biomarker for the PTB detection in subjects with NIDDM (Se = 100%; Sp = 90%).
Journal: Clinical Immunology - Volume 162, January 2016, Pages 107-117