对治疗有反应的慢性HCV患者树突状细胞中肿瘤坏死因子受体1表达上调。

Hepatitis research and treatment Pub Date : 2010-01-01 Epub Date: 2010-08-03 DOI:10.1155/2010/429243
Raul Cubillas, Katherine Kintner, Frances Phillips, Nitin J Karandikar, Dwain L Thiele, Geri R Brown
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引用次数: 11

摘要

目前的研究评估了接受干扰素α/利巴韦林治疗(Ifn/R)的慢性HCV患者外周血单个核细胞(PBMCs)亚群中肿瘤坏死因子受体(TNFR)的表达水平。方法。采用实时荧光定量PCR法(RTPCRs)检测39例HCV+患者和21例对照HCV-患者PBMC中TNFR家族成员mRNA的表达。通过抗cd123、抗cd33、抗TNFR1染色或通过RTPCR检测TNFR1 mRNA,对HCV +患者(未治疗(U)、持续病毒学应答(SVR)和无应答(NR)/复发(Rel)) PBMC进行进一步的亚群分析。结果。在未经治疗的HCV+基因型1患者和对照组中,PBMC中TNFR1 mRNA水平相似。HCV+合并SVR患者PBMC中TNFR1和TNFR2 mRNA水平与HCV(-)患者有统计学差异。从SVR中分离的CD123+ PBMC的TNFR1峰值与NR/Rel之间存在显著差异。结论。TNFR1表达上调,发生在CD123+树突状细胞的一个特定亚群中,出现在HCV+ SVR患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tumor necrosis factor receptor 1 expression is upregulated in dendritic cells in patients with chronic HCV who respond to therapy.

Tumor necrosis factor receptor 1 expression is upregulated in dendritic cells in patients with chronic HCV who respond to therapy.

Tumor necrosis factor receptor 1 expression is upregulated in dendritic cells in patients with chronic HCV who respond to therapy.

Tumor necrosis factor receptor 1 expression is upregulated in dendritic cells in patients with chronic HCV who respond to therapy.

The present studies assessed the level of tumor necrosis factor receptor (TNFR) expression in peripheral blood mononuclear cells (PBMCs) subsets from patients with chronic HCV undergoing interferon α/ribavirin-based therapy (Ifn/R). Methods. TNFR family member mRNA expression was determined using quantitative real-time PCR assays (RTPCRs) in PBMC from 39 HCV+ patients and 21 control HCV- patients. Further subset analysis of HCV + patients (untreated (U), sustained virological responders (SVR), and nonresponders (NR)/relapsers (Rel)) PBMC was performed via staining with anti-CD123, anti-CD33, anti-TNFR1 or via RTPCR for TNFR1 mRNA. Results. A similar level of TNFR1 mRNA in PBMC from untreated HCV+ genotype 1 patients and controls was noted. TNFR1 and TNFR2 mRNA levels in PBMC from HCV+ patients with SVR were statistically different than levels in HCV(-) patients. A significant difference was noted between the peak values of TNFR1 of the CD123+ PBMC isolated from SVR and the NR/Rel. Conclusion. Upregulation of TNFR1 expression, occurring in a specific subset of CD123+ dendritic cells, appeared in HCV+ patients with SVR.

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