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细胞因子基因多态性与土耳其人群皮肤利什曼病易感性的关联。

Association of cytokine gene polymorphisms with susceptibility to cutaneous leishmaniasis in a Turkish population.

机构信息

Department of Medical Microbiology, Faculty of Medicine, Nigde Ömer Halisdemir University, Niğde, Turkey.

Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.

出版信息

Parasite Immunol. 2020 Nov;42(11):e12775. doi: 10.1111/pim.12775. Epub 2020 Jul 30.

Abstract

AIMS

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.

METHODS AND RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法与结果

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。

结论

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。

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