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Circulating granulysin levels in healthcare workers and latent tuberculosis infection estimated using interferon-gamma release assays.

Authors :
Thuong PH
Tam DB
Sakurada S
Hang NT
Hijikata M
Hong LT
Ngoc PT
Anh PT
Cuong VC
Matsushita I
Lien LT
Keicho N
Source :
BMC infectious diseases [BMC Infect Dis] 2016 Oct 18; Vol. 16 (1), pp. 580. Date of Electronic Publication: 2016 Oct 18.
Publication Year :
2016

Abstract

Background: Granulysin (GNLY) is produced by human lymphocyte subpopulations and exhibits antimicrobial activity against Mycobacterium tuberculosis. We examined the association between GNLY levels in blood and latent tuberculosis (TB) infection.<br />Methods: Latency of TB infection among Vietnamese healthcare workers was estimated using interferon-gamma release assays (IGRA), and serum GNLY concentrations were measured using enzyme-linked immunosorbent assays. The levels of GNLY expression in whole blood and the presence of GNLY alleles with the exon-4 polymorphism rs11127 were also determined using PCR-based methods.<br />Results: Among 109 study participants, 41 (37.6 %) were IGRA positive and had significantly lower serum GNLY concentrations compared with IGRA-negative participants (adjusted mean, 95 % confidence interval; 2.03, 1.72-2.44 vs. 2.48, 2.10-2.92 ng/ml, P = 0.0127; analysis of covariance). Serum GNLY concentrations and TB antigen-stimulated interferon-gamma values were weakly inversely correlated (r = -0.20, P = 0.0333). Serum GNLY concentrations varied with GNLY genotypes even after adjustment for gender and age (adjusted P = 0.0015) and were moderately correlated with GNLY expression in blood cells (r = 0.40, P < 0.0001). In subsequent analyses, low serum GNLY concentrations were significantly associated with IGRA status (adjusted odds ratio and 95 % confidence interval, 0.55 and 0.31-0.98, respectively), although GNLY genotype and mRNA levels were not.<br />Conclusions: Decreased GNLY, presumably at the protein level, is linked to the immunological condition of latent TB infection.

Details

Language :
English
ISSN :
1471-2334
Volume :
16
Issue :
1
Database :
MEDLINE
Journal :
BMC infectious diseases
Publication Type :
Academic Journal
Accession number :
27756230
Full Text :
https://doi.org/10.1186/s12879-016-1911-6