Polymorphisms in the RANTES gene increase susceptibility to active tuberculosis in Tunisia

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Abstract

RANTES plays a pivotal role in attracting and activating various leukocyte populations that control Mycobacterium tuberculosis infection. The present study investigated the relationship between the RANTES polymorphisms (-28C/G; rs2280788, and -403G/A; rs2107538) and susceptibility to active tuberculosis (TB) in Tunisian populations. A total of 168 patients with pulmonary TB (pTB), 55 with extrapulmonary TB (epTB), and 150 control subjects were studied. Genotype analyses were carried out using polymerase chain reaction-restriction fragment length polymorphism method. We found that the -28 GG genotype was significantly associated with susceptibility to pTB (odds ratio [OR]=11.19; 95% confidence intervals [CI], 5.14-25; P corrected for the number of genotypes [Pc]=10 -8) and epTB (OR=11.67; 95% CI, 4.74-29.33; Pc=10 -8). However, the -28 CC genotype was found to be significantly associated with resistance to pTB (OR=0.08; 95% CI, 0.04-0.16; Pc=10 -8) and epTB development (OR=0.11; 95% CI, 0.05-0.27; Pc=10 -8). -403A allele was associated with increased risk development of epTB (OR=2.21; 95% CI, 1.18-4.14; p=0.007). G-G and A-C haplotypes and the AG/GC diplotype were associated with increase susceptibility to pTB (OR=7.88, 95% CI, 5.38-11.55; Pc=3.10 -8; OR=2.32, 95% CI, 1.32-4.11; Pc=3.10 -3; OR=13.26, 95% CI, 6.06-29.89; Pc=3.10 -8; respectively) and epTB (OR=6.64, 95% CI, 4-11.05; Pc=3.10 -8; OR=2.6, 95% CI, 1.26-5.35; Pc=12.10 -3; OR=11.26, 95% CI, 4.44-29.28; Pc=3.10 -8; respectively). Collectively, our findings suggested an association of the RANTES -28C/G and -403G/A functional polymorphisms with susceptibility to Mycobacterium tuberculosis infection in Tunisian populations. © Copyright 2011, Mary Ann Liebert, Inc.

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Ben-Selma, W., Harizi, H., Bougmiza, I., Kahla, I. B., Letaief, M., & Boukadida, J. (2011). Polymorphisms in the RANTES gene increase susceptibility to active tuberculosis in Tunisia. DNA and Cell Biology, 30(10), 789–800. https://doi.org/10.1089/dna.2010.1200

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