Department of Medical Microbiology, Faculty of Medicine, Nigde Ömer Halisdemir University, Niğde, Turkey.
Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Parasite Immunol. 2020 Nov;42(11):e12775. doi: 10.1111/pim.12775. Epub 2020 Jul 30.
The objective of this study was to determine the association of TNF-α -308 G/A, IFN-γ +874 T/A, IL-12B + 1188 A/C, IL-10 -1082 G/A and IL-4 -590 C/T polymorphisms with susceptibility to CL.
A total of 55 CL patients and 110 controls from Sanlıurfa province of Turkey were included to this study. Polymorphisms were genotyped by 'polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP)' and 'amplification refractory mutation system-PCR (ARMS-PCR)' methods. A statistically significant difference was noted in the allele (P < .001, P = .002) and genotype (P < .001, P = .001,) frequencies of TNF-α -308 G/A and IL-4 -590 C/T, respectively. TNF-α 308 GG versus GA genotype (OR = 19.556 [95% CI 8.310-46.019] P < .001), GG versus GA + AA genotype (OR = 20.444 [95% CI 8.707-48.004] P < .001) and G versus A allele (OR = 6.968 [95% CI 3.903-12.440] P < .001) revealed significant association with CL. IL-4 -590 CC versus TT + CT genotype (OR = 2.049 [95% CI 1.025-4.096], P = .041) and C versus T allele (OR = 2.441 [95% CI 1.355-4.396], P = .002) revealed significant association with CL.
Our study indicates that TNF-α 308 G/A and IL-4-590 C/T polymorphisms are significantly associated with susceptibility to CL. Individuals carrying A allele at TNF-α promoter -308 position and T allele at IL-4 promoter -590 position are at a higher risk for CL.
本研究旨在确定 TNF-α-308 G/A、IFN-γ+874 T/A、IL-12B+1188 A/C、IL-10-1082 G/A 和 IL-4-590 C/T 多态性与 CL 易感性的关联。
本研究共纳入 55 例 CL 患者和 110 例来自土耳其桑利乌尔法省的对照者。通过“聚合酶链反应-限制性片段长度多态性(PCR-RFLP)”和“扩增受阻突变系统-PCR(ARMS-PCR)”方法对多态性进行基因分型。TNF-α-308 G/A 和 IL-4-590 C/T 的等位基因(P<.001,P=.002)和基因型(P<.001,P=.001)频率存在统计学差异。TNF-α 308 GG 与 GA 基因型(OR=19.556[95%CI 8.310-46.019],P<.001)、GG 与 GA+AA 基因型(OR=20.444[95%CI 8.707-48.004],P<.001)和 G 等位基因(OR=6.968[95%CI 3.903-12.440],P<.001)与 CL 显著相关。IL-4-590 CC 与 TT+CT 基因型(OR=2.049[95%CI 1.025-4.096],P=.041)和 C 等位基因(OR=2.441[95%CI 1.355-4.396],P=.002)与 CL 显著相关。
本研究表明 TNF-α-308 G/A 和 IL-4-590 C/T 多态性与 CL 易感性显著相关。TNF-α 启动子-308 位置携带 A 等位基因和 IL-4 启动子-590 位置携带 T 等位基因的个体患 CL 的风险更高。