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白细胞介素-10 启动子多态性预测慢性乙型肝炎对干扰素 alfa 的初始反应。

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

机构信息

Department of Infectious Diseases, the Fuzhou General Hospital, Fu Zhou, Fujian Province 350003, China.

出版信息

Virol J. 2011 Jan 20;8:28. doi: 10.1186/1743-422X-8-28.

Abstract

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.

摘要

为了研究白细胞介素 10 启动子多态性的变异是否能预测慢性乙型肝炎患者对干扰素 alfa(IFN-α)治疗的持续应答的可能性,采用聚合酶链反应(PCR)-裸露技术、限制性内切酶消化或直接测序,检测了 52 例慢性乙型肝炎患者 IL-10 基因启动子中 3 个双等位基因多态性的遗传。在 24 例对干扰素 alfa-2b 具有病毒学持续应答(SR)和 28 例无应答(NR)的慢性 HBV 感染患者中研究了其与抗病毒治疗结局的关系。与 NR 相比,SR 中存在更多的 -592A 等位基因、-592A/A 基因型和 -1082/-1819/-592 ATA 单倍型。携带-592A 等位基因、-592A/A 基因型和-1082/-1819/-592 ATA 单倍型与 SR 相关。我们的研究结果表明,IL-10 基因启动子区域的异质性在决定慢性乙型肝炎对 IFN-α治疗的初始反应中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d3/3034702/484d21336f64/1743-422X-8-28-1.jpg

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