Author/Authors :
Mostafavi-Pour, Zohreh Recombinant Protein Laboratory - Department of Biochemistry - School of Medicine, Shiraz University of Medical Sciences , Safaee Ardekani, Leila Recombinant Protein Laboratory - Department of Biochemistry - School of Medicine, Shiraz University of Medical Sciences , Zare, Razie Recombinant Protein Laboratory - Department of Biochemistry - School of Medicine, Shiraz University of Medical Sciences , Mokarram, Pooneh Recombinant Protein Laboratory - Department of Biochemistry - School of Medicine, Shiraz University of Medical Sciences , Movahedi, Bahram Recombinant Protein Laboratory - Department of Biochemistry - School of Medicine, Shiraz University of Medical Sciences , Hemmati, Mina Department of Biochemistry - Faculty of Medicine, Birjand University of Medical Sciences , Mosavari, Nader Department of PPD Tuberculin - Razi Vaccine and Serum Research Institute, Tehran,
Abstract :
Background: Discriminating latent tuberculosis infection
(LTBI) from active TBI may be challenging. The objective of this
study was to produce the recombinant L-alanine dehydrogenase
(AlaDH) antigen and evaluate individuals with LTBI, those
with active TBI, and uninfected individuals by enzyme-linked
immunospot assay (ELISPOT) in order to distinguish LTBI
from active TBI.
Methods: This exploratory study was performed in the Iranian
city of Shiraz from 2014 to 2015. The study population (N=99)
was divided into 3 groups: individuals with newly diagnosed
active TBI (n=33), their household contacts (n=33), and
controls (n=33). AlaDH was produced through PCR and cloning
methods. The diagnostic characteristics of AlaDH vs. ESAT-6/
CFP-10 were evaluated in responses to interferon-γ (IFN-γ)
and interleukin-2 (IL-2) with ELISPOT. Differences between
the groups were assessed with the Kruskal–Wallis and Mann–
Whitney tests for nonparametric data analysis. The statistical
analyses were performed with SPSS, version 16.
Results: IFN-γ responses to both ESAT-6/CFP-10 (P=0.81)
and AlaDH (P=0.18) revealed that there were no significant
differences between the individuals with LTBI and those with
active TBI. The same results were determined for IL-2 responses
to ESAT-6/CFP-10 between the 2 groups, while significantly
higher IL-2 responses to AlaDH were observed in LTBI than
in active TBI. According to the ROC curve analysis, a cutoff
value of 275 SFC showed sensitivity of 75.8% and specificity
of 78.8% for distinguishing LTBI from active TBI by IL-2
responses to AlaDH.
Keywords :
Interferon-gamma , Interleukin-2 , Enzyme-linked immunospot assay , Mycobacterium tuberculosis