Ghamari Ehsan, Farnia Poopak, Saif Shima, Marashian Mehran, Ghanavi Jaladein, Farnia Parissa, Velayati Ali Akbar
Mycobacteriology Research Centre (MRC), National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical Sciences Tehran, Iran.
Mycobacteriology Research Centre (MRC), National Research Institute of Tuberculosis and Lung Disease (NRITLD), Shahid Beheshti University of Medical SciencesTehran, Iran; Department of Biotechnology, Advanced Technologies in Medicine, Shahid Beheshti University of Medical SciencesTehran, Iran.
Am J Clin Exp Immunol. 2016 Nov 30;5(4):55-61. eCollection 2016.
Since apoptosis and survival of the immune cells are crucially important in prevention or predisposition of individual from/to infections, especially in intracellular ones, the current study was performed to assess the correlation of host genetic polymorphisms with susceptibility to TB. For this reason, we investigated the difference of the single nucleotide polymorphisms [SNPs] in tumor necrosis factors [TNF-α] genes at (-238, -308, -857 and -863 position) and tumor necrosis factors receptors two [TNFR2] at (T 587 G position) between patients [n=151] and control [n=83]. The genotyping was studied by using PCR-RFLP which had high sensitivity in detecting compared with other techniques. The results showed a strong correlation between two polymorphisms in different loci of TNF-α gene including TNF-α T-857 C and A 238 G. But no association were found in TNFR2 genes with susceptibility to TB. And we found no correlation between TNFR2 and TNF-α gene polymorphisms. Therefore, the TNF-α T 857 C and A 238 G SNPs could be promising marker for identifying risk populations.
由于免疫细胞的凋亡和存活在个体预防感染或易感性方面至关重要,尤其是在细胞内感染中,因此开展了本研究以评估宿主基因多态性与结核病易感性之间的相关性。为此,我们调查了151例患者和83例对照者之间肿瘤坏死因子(TNF-α)基因在(-238、-308、-857和-863位点)的单核苷酸多态性(SNP)以及肿瘤坏死因子受体2(TNFR2)在(T587G位点)的差异。采用PCR-RFLP进行基因分型,与其他技术相比,该方法在检测方面具有高灵敏度。结果显示,TNF-α基因不同位点的两个多态性之间存在强相关性,包括TNF-α T-857C和A238G。但未发现TNFR2基因与结核病易感性之间存在关联。并且我们发现TNFR2与TNF-α基因多态性之间无相关性。因此,TNF-α T857C和A238G SNP可能是识别风险人群的有前景的标志物。