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Interleukin-10 promoter polymorphism predicts initial response of chronic hepatitis B to interferon alfa

机译:Interleukin-10启动子多态性预测慢性乙型肝炎对干扰素α的初始反应

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摘要

In order to examine whether variation in interleukin-10 promoter polymorphism would predict the likelihood of sustain response of chronic hepatitis B to treatment with interferon alfa (IFN-α), the inheritance of 3 biallelic polymorphisms in the IL-10 gene promoter in patients with 52 chronic hepatitis B were determined by polymerase chain reaction (PCR)-bared techniques, restriction enzyme digestion or direct sequencing. The relationship to the outcome of antiviral therapy for chronic HBV infection was studied in 24 patients who had a virologically sustained response(SR) and in 28 non-responder(NR) to interferon alfa-2b and several IL-10 variants were more frequent among SR compared with NR. Carriage of the -592A allele, -592A/A genotype and -1082/-1819/-592 ATA haplotype was associated with SR. Our findings indicate that heterogeneity in the promoter region of the IL-10 gene has a role in determining the initial response of chronic hepatitis B to IFN-α therapy.
机译:为了检查白介素10启动子多态性的变异是否可以预测慢性乙型肝炎对干扰素α(IFN-α)治疗的持续反应的可能性,对IL-10基因启动子中3种双等位基因多态性的遗传通过裸露的聚合酶链反应(PCR)技术,限制酶消化或直接测序法确定了52例慢性乙型肝炎。研究了24例对病毒性持续反应(SR)有病毒学持续应答(SR)的患者和28例对干扰素alfa-2b无应答者(NR)的抗病毒治疗与慢性HBV感染抗病毒治疗结果之间的关系,其中几种IL-10变体更为频繁SR与NR相比。 -592A等位基因,-592A / A基因型和-1082 / -1819 / -592 ATA单体型的携带与SR相关。我们的发现表明,IL-10基因启动子区域的异质性决定了慢性乙型肝炎对IFN-α治疗的初始反应。

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