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TNFSF14及其受体LTβR和HVEM在病毒肝炎中的作用

李桂清 尚宇航 曹朝晖 杨菲 郑权友 王庆红 许桂莲

中国免疫学杂志2015,Vol.31Issue(12):1591-1594,4.
中国免疫学杂志2015,Vol.31Issue(12):1591-1594,4.DOI:10.3969/j.issn.1000-484X.2015.12.002

TNFSF14及其受体LTβR和HVEM在病毒肝炎中的作用

Role of TNFSF14 and its receptors LTβR and HVEM in pathogenesis of virus hepatitis

李桂清 1尚宇航 1曹朝晖 1杨菲 1郑权友 2王庆红 3许桂莲1

作者信息

  • 1. 第三军医大学基础部免疫学教研室,重庆 400038
  • 2. 第三军医大学附属大坪医院泌尿外科,重庆 400042
  • 3. 重庆医科大学附属儿童医院儿科研究所流式细胞室,重庆 400014
  • 折叠

摘要

Abstract

Objective:To explore the role of TNFSF14 and its receptors LTβR and HVEM in the pathogenesis of virus hepatitis.Methods:Marine fulminant viral hepatitis model was established by infecting mice with MHV-3.Liver tissue destruction in LIGHT KO and WT mice were analyzed by HE staining and ALT levels in serum by automatic biochemical analyzer .The mRNA levels of HVEM and LTβR in the liver and spleen tissues in the indicated time points ( 0 h, 12 h, 24 h, 48 h, 72 h ) were detected by quantitative-PCR.The expression of HVEM and LTβR on PBMC in patients with severe hepatitis were measured by flow cytometry.Results:In the MHV-3-induced murine fulminant hepatitis model ,liver injury in LIGHT KO mice was obviously decreased than that of WT mice,and ALT levels was also significantly lower than that of WT mice (P<0.01).The mRNA of HVEM and LTβR in the spleen were increased significantly after 48 h postinfection with MHV-3 ( P<0.05 );The level of LTβR mRNA in liver was significantly up-regulated in 12 h postinfection with MHV-3(P<0.01).Compared to healthy volunteers,the expression of both HVEM and LTβR on PBMC in patients with severe hepatitis was remarkably enhanced .Conclusion: TNFSF14 and its receptors LTβR and HVEM play a critical role in the pathogenesis of viral fulminant hepatitis .

关键词

TNFSF14/LTβR/HVEM/病毒性肝炎

Key words

TNFSF14/LTβR/HVEM/Viral hepatitis

分类

医药卫生

引用本文复制引用

李桂清,尚宇航,曹朝晖,杨菲,郑权友,王庆红,许桂莲..TNFSF14及其受体LTβR和HVEM在病毒肝炎中的作用[J].中国免疫学杂志,2015,31(12):1591-1594,4.

基金项目

本文受国家自然科学基金面上项目(31270929)和重庆市自然科学基金面上项目(cstc2013jcyjA10129)资助. (31270929)

中国免疫学杂志

OA北大核心CSCDCSTPCD

1000-484X

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