丙型肝炎病毒NS3蛋白的组织表达与慢性丙型肝炎患者的组织学或临床特征无关。

Chang Gung medical journal Pub Date : 2011-05-01
Wei-Hsuan Liao, Shui-Yi Tung, Cheng-Han Shen, Kam-Fai Lee, Cheng-Shyong Wu
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引用次数: 0

摘要

背景:在慢性乙型肝炎中,肝组织中HBcAg病毒蛋白与血清转氨酶水平、血清乙型肝炎病毒DNA和组织学活性呈正相关。目前尚不清楚慢性丙型肝炎是否也存在类似的关系。本研究试图确定丙型肝炎病毒(HCV-NS3)肝细胞NS3蛋白的表达是否与血清HCV-RNA载量、肝炎活度或其他临床参数相关。方法:回顾性分析214例慢性丙型肝炎患者的临床和组织学资料。采用小鼠单克隆抗体检测肝细胞中的HCV-NS3。将染色强度半定量评分为0~3+,并分析其与血清HCV-RNA载量、肝炎活动性等临床参数的相关性。结果:214例肝活检中HCV-NS3阳性202例(94%),HCV-NS3染色强度12例(6%)为0,181例(84%)为1+,21例(10%)为2+。样本中HCV- ns3表达强度与患者年龄(p = 0.302,方差分析)、患者性别(p = 0.130, Fisher确切检验)、丙氨酸转氨酶水平(p = 0.177,方差分析)、血清HCV- rna水平(p = 0.305,方差分析)、HCV抗体滴度(p = 0.139, χ 2检验)、肝炎活动性指数评分(p = 0.861, χ 2检验)、持续病毒反应率(p = 0.861, χ 2检验)无关。结论:HCV- ns3免疫组化染色法检测肝标本HCV是可靠的。肝细胞表达HCV-NS3与血清病毒载量、肝损伤严重程度或治疗反应无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue expression of the hepatitis C virus NS3 protein does not correlate with histological or clinical features in patients with chronic hepatitis C.

Background: In chronic hepatitis B, the HBcAg viral protein in liver tissue demonstrates a positive correlation with serum aminotransferase levels, serum hepatitis B viral DNA, and histological activities. Little is known if similar relationships exist for chronic hepatitis C. This study attempted to determine if expression of the hepatocyte NS3 protein of the hepatitis C virus (HCV-NS3) was correlated with the serum HCV-RNA load, hepatitis activity, or other clinical parameters.

Methods: Clinical and histological data of 214 patients with chronic hepatitis C were retrospectively reviewed. A mouse monoclonal antibody was used to detect HCV-NS3 in hepatocytes. The staining intensity was scored semiquantitatively as 0~3+, and its correlations with the serum HCV-RNA load, hepatitis activity, and other clinical parameters were analyzed.

Results: In total, 202 (94%) of the 214 liver biopsies were positive for HCV-NS3, and the intensity of HCV-NS3 staining was 0 in 12 (6%), 1+ in 181 (84%), and 2+ in 21 patients (10%). The intensity of HCV-NS3 expression in the samples did not correlate with patient age (p = 0.302, ANOVA), patient gender (p = 0.130, Fisher's exact test), the alanine transaminase level (p = 0.177, ANOVA), serum HCV-RNA level (p = 0.305, ANOVA), HCV antibody titer (p = 0.139, Chi-squared test), hepatitis activity index score (p = 0.861, Chisquared test), or sustained viral response rate (p = 0.861, Chi-squared test).

Conclusions: This HCV-NS3 immunohistochemical staining method was reliable for detecting HCV in liver specimens. Hepatocyte expression of HCV-NS3 was not correlated with the serum viral load, severity of hepatic injury, or treatment response.

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