Bhagwan Mahavir Medical Research Centre, Hyderabad, India.
Scand J Immunol. 2014 Mar;79(3):197-205. doi: 10.1111/sji.12136.
Cytokine gene polymorphisms are known to be associated with functional differences in cytokine regulation and may affect host susceptibility to tuberculosis (TB). Contacts are important group in developing tuberculosis infection and are 10-60 times more likely to develop TB than general population. The present study was carried out in patients with TB (N = 176), their household contacts (HHC; N = 155) from Free Chest TB Clinic PPM DOTS (1TU) covering 500,000 population at Mahavir Hospital and Research Centre, Hyderabad, and healthy controls (HC; N = 170) also included. The association of single-nucleotide polymorphisms (SNPs) in the promoter region of TNF-α (-308G/A), IL-2 (-330T/G), IL-4 (-589C/T) and in exon region of TGF-β1 (+869T/C) genes was assessed by ARMS & PCR-RFLP using specific primers in the above-mentioned subjects. The differences in allelic or genotypic frequencies of TNF-α (-308G/A) between patients, their HHC and HC were not statistically significant (P > 0.05). IL-2 (-330T/G) TG genotype was significantly different between patients, HHC compared to HC (P < 0.002, OR-1.997, 95%CI-1.260-3.168, P < 0.03, OR-1.602, 955CI-1.003-2.561).IL-4 (-589C/T) CC genotype was significantly different between patients and HC (P < 0.03, OR-1.791, 95%CI-1.009-3.189) as well as between HHC and HC at P < 0.0001, OR-2.56, 95%CI-1.448-4.545. In addition, the TGF-β 1 (+869T/C) TC genotype was significantly associated with susceptibility to tuberculosis in patients when compared against HC(P < 0.0001, OR-3.416, 95%CI-2.063-5.670) and HHC (P < 0.0001, OR-2.357, 95%CI-1.439-3.868), respectively.MDR analysis indicated that TT genotype of TGF-β1 with TT and CT genotypes of IL-4 showed high risk with GA, TT genotypes of TNF-α, IL-2, respectively. Our results suggest that IL-2 (-330T/G), IL-4 (-589 C/T) and TGF-β1 (+869T/C) gene polymorphisms may be associated with TB susceptibility.
细胞因子基因多态性与细胞因子调节的功能差异有关,可能影响宿主对结核病(TB)的易感性。接触者是发展结核感染的重要群体,比一般人群更容易患结核病(TB),患病风险是 10-60 倍。本研究在来自 PPM DOTS(1TU)免费胸部结核病诊所的结核病(TB)患者(N=176)、其家庭接触者(HHC;N=155)和健康对照者(HC;N=170)中进行。使用特定引物,通过 ARMS 和 PCR-RFLP 评估 TNF-α(-308G/A)、IL-2(-330T/G)、IL-4(-589C/T)和 TGF-β1(+869T/C)基因启动子区域的单核苷酸多态性(SNP)。患者、其 HHC 和 HC 之间 TNF-α(-308G/A)的等位基因或基因型频率差异无统计学意义(P>0.05)。与 HC 相比,患者和 HHC 之间的 IL-2(-330T/G)TG 基因型差异显著(P<0.002,OR-1.997,95%CI-1.260-3.168,P<0.03,OR-1.602,955CI-1.003-2.561)。IL-4(-589C/T)CC 基因型在患者与 HC 之间(P<0.03,OR-1.791,95%CI-1.009-3.189)以及 HHC 与 HC 之间差异显著(P<0.0001,OR-2.56,95%CI-1.448-4.545)。此外,与 HC 相比,TGF-β1(+869T/C)TC 基因型与患者的结核病易感性显著相关(P<0.0001,OR-3.416,95%CI-2.063-5.670)和 HHC(P<0.0001,OR-2.357,95%CI-1.439-3.868)。多因素回归分析表明,TGF-β1 的 TT 基因型与 IL-4 的 TT 和 CT 基因型、TNF-α、IL-2 的 TT 基因型具有高风险。我们的结果表明,IL-2(-330T/G)、IL-4(-589C/T)和 TGF-β1(+869T/C)基因多态性可能与结核病易感性有关。