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Insulin resistance impairs sustained response rate to peginterferon plus ribavirin in chronic hepatitis C patients.胰岛素抵抗会损害慢性丙型肝炎患者对聚乙二醇干扰素加利巴韦林的持续应答率。
Gastroenterology. 2005 Mar;128(3):636-41. doi: 10.1053/j.gastro.2004.12.049.
2
CXCR3, IP-10, and Mig are required for CD4+ T cell recruitment during the DTH response to HSV-1 yet are independent of the mechanism for viral clearance.在对单纯疱疹病毒1型的迟发型超敏反应中,CD4+T细胞募集需要CXCR3、IP-10和Mig,但它们与病毒清除机制无关。
Virology. 2005 Mar 1;333(1):1-9. doi: 10.1016/j.virol.2005.01.005.
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Gene expression profile of T-cell-specific chemokines in human hepatocyte-derived cells: evidence for a synergistic inducer effect of cytokines and hepatitis C virus proteins.人肝细胞衍生细胞中T细胞特异性趋化因子的基因表达谱:细胞因子与丙型肝炎病毒蛋白协同诱导作用的证据
J Viral Hepat. 2005 Jan;12(1):27-37. doi: 10.1111/j.1365-2893.2005.00540.x.
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Predictors of response to therapy for chronic hepatitis C.慢性丙型肝炎治疗反应的预测因素。
Semin Liver Dis. 2004;24 Suppl 2:25-31. doi: 10.1055/s-2004-832925.
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Association of serum interleukin-8 with virologic response to antiviral therapy in patients with chronic hepatitis C.慢性丙型肝炎患者血清白细胞介素-8与抗病毒治疗病毒学应答的相关性
J Hepatol. 2004 May;40(5):845-52. doi: 10.1016/j.jhep.2004.01.007.
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Host factors and failure of interferon-alpha treatment in hepatitis C virus.宿主因素与丙型肝炎病毒α干扰素治疗失败
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7
Peginterferon-alpha2a and ribavirin combination therapy in chronic hepatitis C: a randomized study of treatment duration and ribavirin dose.聚乙二醇干扰素α-2a与利巴韦林联合治疗慢性丙型肝炎:治疗疗程和利巴韦林剂量的随机研究
Ann Intern Med. 2004 Mar 2;140(5):346-55. doi: 10.7326/0003-4819-140-5-200403020-00010.
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Increased circulating and intrahepatic T-cell-specific chemokines in chronic hepatitis C: relationship with the type of virological response to peginterferon plus ribavirin combination therapy.慢性丙型肝炎患者循环及肝内T细胞特异性趋化因子水平升高:与聚乙二醇干扰素联合利巴韦林治疗病毒学反应类型的关系
Aliment Pharmacol Ther. 2004 Mar 1;19(5):551-62. doi: 10.1111/j.1365-2036.2004.01872.x.
9
Predicting the therapeutic response in patients with chronic hepatitis C: the role of viral kinetic studies.预测慢性丙型肝炎患者的治疗反应:病毒动力学研究的作用。
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10
Expression of the chemokine IP-10 (CXCL10) by hepatocytes in chronic hepatitis C virus infection correlates with histological severity and lobular inflammation.在慢性丙型肝炎病毒感染中,肝细胞趋化因子IP-10(CXCL10)的表达与组织学严重程度及小叶炎症相关。
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1型慢性丙型肝炎感染患者治疗前血清干扰素γ诱导蛋白10水平与聚乙二醇干扰素联合利巴韦林治疗持续病毒学应答的相关性

Association of pretreatment serum interferon gamma inducible protein 10 levels with sustained virological response to peginterferon plus ribavirin therapy in genotype 1 infected patients with chronic hepatitis C.

作者信息

Diago M, Castellano G, García-Samaniego J, Pérez C, Fernández I, Romero M, Iacono O L, García-Monzón C

机构信息

Section of Hepatology, University General Hospital, Valencia, Spain.

出版信息

Gut. 2006 Mar;55(3):374-9. doi: 10.1136/gut.2005.074062. Epub 2005 Sep 8.

DOI:10.1136/gut.2005.074062
PMID:16150856
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1856069/
Abstract

BACKGROUND

Increased serum and intrahepatic interferon gamma inducible protein 10 (IP-10) levels in patients with chronic hepatitis C (CHC) have been described.

AIM

To analyse the possible association of serum IP-10 levels with different outcomes to antiviral therapy.

PATIENTS

A total of 137 CHC patients treated with peginterferon plus ribavirin.

METHODS

Serum IP-10 levels were determined by enzyme linked immunosorbent assay before therapy, after 12 weeks of treatment, and 24 weeks after cessation of therapy. Variables significantly associated with a sustained virological response (SVR) on univariate analysis were included in a multivariate logistic regression model.

RESULTS

Pretreatment serum IP-10 levels in patients with SVR were significantly lower than in non-responders (NR) (332.4 (222.1) v 476.8 (305.3) pg/ml, respectively; p=0.004). Serum IP-10 concentrations significantly decreased in patients with SVR (pretreatment: 332.4 (222.1) pg/ml; post-treatment: 170.2 (140.1) pg/ml; p<0.001) but not in NR (pretreatment: 476.8 (305.3) pg/ml; post treatment: 387.3 (268.1) pg/ml; p=0.06). By multivariate analysis, non-1 genotype (odds ratio (OR) 3.5 (95% confidence interval (CI) 1.1-10.4); p=0.003) and low viral load at baseline (OR 0.34 (95% CI 0.14-0.79); p=0.01) were independent predictors of SVR in all patients. When multivariate analysis was restricted to patients with genotype 1, only baseline viral load (OR 0.38 (95% CI 0.155-0.96); p=0.04) and pretreatment serum IP-10 levels (OR 0.99 (95% CI 0.996-0.999); p=0.03) were identified as predictive factors of SVR.

CONCLUSION

Pretreatment serum IP-10 behaves as a predictive factor of SVR to peginterferon plus ribavirin therapy in genotype 1 infected patients.

摘要

背景

已有报道称慢性丙型肝炎(CHC)患者血清及肝内干扰素γ诱导蛋白10(IP-10)水平升高。

目的

分析血清IP-10水平与抗病毒治疗不同结局之间的可能关联。

患者

共137例接受聚乙二醇干扰素联合利巴韦林治疗的CHC患者。

方法

采用酶联免疫吸附测定法在治疗前、治疗12周后及治疗停止后24周测定血清IP-10水平。单因素分析中与持续病毒学应答(SVR)显著相关的变量纳入多因素逻辑回归模型。

结果

SVR患者治疗前血清IP-10水平显著低于无应答者(NR)(分别为332.4(222.1)与476.8(305.3)pg/ml;p = 0.004)。SVR患者血清IP-10浓度显著降低(治疗前:332.4(222.1)pg/ml;治疗后:170.2(140.1)pg/ml;p < 0.001),但NR患者未降低(治疗前:476.8(305.3)pg/ml;治疗后:387.3(268.1)pg/ml;p = 0.06)。多因素分析显示,非1基因型(比值比(OR)3.5(95%置信区间(CI)1.1 - 10.4);p = 0.003)和基线低病毒载量(OR 0.34(95% CI 0.14 - 0.79);p = 0.01)是所有患者SVR的独立预测因素。当多因素分析仅限于1基因型患者时,仅基线病毒载量(OR 0.38(95% CI 0.155 - 0.96);p = 0.04)和治疗前血清IP-10水平(OR 0.99(95% CI 0.996 - 0.999);p = 0.03)被确定为SVR的预测因素。

结论

治疗前血清IP-10是1基因型感染患者对聚乙二醇干扰素联合利巴韦林治疗SVR的预测因素。