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IL-28B polymorphisms and the response to antiviral therapy in HCV genotype 2 and 3 varies by ethnicity: a meta-analysis.IL-28B 多态性与 HCV 基因型 2 和 3 对抗病毒治疗的反应因种族而异:一项荟萃分析。
J Viral Hepat. 2013 Jun;20(6):377-84. doi: 10.1111/jvh.12039. Epub 2013 Jan 7.
2
Sofosbuvir for previously untreated chronic hepatitis C infection.索磷布韦片治疗未经治疗的慢性丙型肝炎感染。
N Engl J Med. 2013 May 16;368(20):1878-87. doi: 10.1056/NEJMoa1214853. Epub 2013 Apr 23.
3
Meta-analysis: IL28B polymorphisms predict sustained viral response in HCV patients treated with pegylated interferon-α and ribavirin.荟萃分析:IL28B 多态性可预测聚乙二醇干扰素-α和利巴韦林治疗的 HCV 患者的持续病毒应答。
Aliment Pharmacol Ther. 2012 Jul;36(2):91-103. doi: 10.1111/j.1365-2036.2012.05131.x. Epub 2012 May 16.
4
An update on treatment of genotype 1 chronic hepatitis C virus infection: 2011 practice guideline by the American Association for the Study of Liver Diseases.1型慢性丙型肝炎病毒感染治疗的最新进展:美国肝病研究协会2011年实践指南
Hepatology. 2011 Oct;54(4):1433-44. doi: 10.1002/hep.24641. Epub 2011 Sep 26.
5
Limited use of interleukin 28B in the setting of response-guided treatment with detailed on-treatment virological monitoring.在基于详细治疗中病毒学监测的应答指导治疗中,白细胞介素 28B 的应用有限。
Hepatology. 2011 Sep 2;54(3):772-80. doi: 10.1002/hep.24458. Epub 2011 Jul 21.
6
Interleukin 28B gene variation at rs12979860 determines early viral kinetics during treatment in patients carrying genotypes 2 or 3 of hepatitis C virus.白细胞介素 28B 基因变异 rs12979860 决定了携带丙型肝炎病毒基因型 2 或 3 的患者在治疗过程中的早期病毒动力学。
J Infect Dis. 2011 Jun 15;203(12):1748-52. doi: 10.1093/infdis/jir193.
7
Complementary role of vitamin D deficiency and the interleukin-28B rs12979860 C/T polymorphism in predicting antiviral response in chronic hepatitis C.维生素 D 缺乏与白细胞介素-28B rs12979860 C/T 多态性在预测慢性丙型肝炎抗病毒反应中的互补作用。
Hepatology. 2011 Apr;53(4):1118-26. doi: 10.1002/hep.24201.
8
IL28B polymorphisms, IP-10 and viral load predict virological response to therapy in chronic hepatitis C.IL28B 多态性、IP-10 和病毒载量可预测慢性丙型肝炎治疗的病毒学应答。
Aliment Pharmacol Ther. 2011 May;33(10):1162-72. doi: 10.1111/j.1365-2036.2011.04635.x. Epub 2011 Mar 28.
9
IL28B genetic variation and treatment response in patients with hepatitis C virus genotype 3 infection.IL28B 基因变异与丙型肝炎病毒基因型 3 感染患者的治疗反应。
Hepatology. 2011 Mar;53(3):746-54. doi: 10.1002/hep.24154.
10
EASL Clinical Practice Guidelines: management of hepatitis C virus infection.欧洲肝脏研究学会临床实践指南:丙型肝炎病毒感染的管理
J Hepatol. 2011 Aug;55(2):245-64. doi: 10.1016/j.jhep.2011.02.023. Epub 2011 Mar 1.

白细胞介素 28B 多态性可预测丙型肝炎病毒基因型 2 和 3 感染患者的应答。

Interleukin 28B polymorphisms as predictor of response in hepatitis C virus genotype 2 and 3 infected patients.

机构信息

Alessandra Mangia, Leonardo Mottola, Rosanna Santoro, Liver Unit-IRCCS, "Casa Sollievo della Sofferenza", San Giovanni Rotondo, 71013 FG, Italy.

出版信息

World J Gastroenterol. 2013 Dec 21;19(47):8924-8. doi: 10.3748/wjg.v19.i47.8924.

DOI:10.3748/wjg.v19.i47.8924
PMID:24379617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3870545/
Abstract

Single nucleotide polymorphisms near the interleukin 28B (IL-28B) gene have been identified as strong predictors of both spontaneous or Peg-interferon (Peg-IFN) and ribavirin (RBV) induced clearance of hepatitis C virus (HCV). Several studies have shown that, in patients with genotype 1 (GT-1), rs12979860 C/C and rs8099917 T/T substitutions are associated with a more than twofold increase in sustained virological response rate to Peg-IFN and RBV treatment. Although new treatment regimens based on combination of DAA with or without IFN are in the approval phase, until combination regimens with a backbone of Peg-IFN will be used, we can expect that IL28B holds its importance. The clinical relevance of IL28B genotyping in treatment of patients infected with HCV genotype 2 (GT-2) and 3 (GT-3) remains controversial. Therefore, after a careful examination of the available literature, we analyzed the impact of IL28B in GT-2 and -3. Simple size of the studies and GT-2 and GT-3 proportion were discussed. An algorithm for the practical use of IL28B in these patients was suggested at the aim of optimizing treatment.

摘要

白细胞介素 28B(IL-28B)基因附近的单核苷酸多态性已被确定为自发性或聚乙二醇干扰素(Peg-IFN)和利巴韦林(RBV)诱导丙型肝炎病毒(HCV)清除的强有力预测因子。多项研究表明,在基因型 1(GT-1)患者中,rs12979860 C/C 和 rs8099917 T/T 取代与 Peg-IFN 和 RBV 治疗持续病毒学应答率增加两倍以上相关。尽管基于 DAA 与 IFN 联合或不联合的新治疗方案处于批准阶段,但在使用 Peg-IFN 作为骨干的联合方案之前,我们可以预期 IL28B 仍然具有重要意义。IL28B 基因分型在治疗丙型肝炎基因型 2(GT-2)和 3(GT-3)感染患者中的临床相关性仍存在争议。因此,在仔细检查了现有文献后,我们分析了 IL28B 在 GT-2 和 GT-3 中的作用。讨论了研究的简单规模和 GT-2 和 GT-3 的比例。为了优化治疗,针对这些患者提出了 IL28B 的实际应用算法。