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Pathogenesis of coxsackievirus B3-induced myocarditis: role of macrophage migration inhibitory factor

YU Xiao-hua LI Shuang-jie CHEN Rui-zhen YANG Ying-zhen ZHANG Ping

中华医学杂志(英文版)2012,Vol.125Issue(1):50-55,6.
中华医学杂志(英文版)2012,Vol.125Issue(1):50-55,6.DOI:10.3760/cma.j.issn.0366-6999.2012.01.010

Pathogenesis of coxsackievirus B3-induced myocarditis: role of macrophage migration inhibitory factor

Pathogenesis of coxsackievirus B3-induced myocarditis: role of macrophage migration inhibitory factor

YU Xiao-hua 1LI Shuang-jie 2CHEN Rui-zhen 3YANG Ying-zhen 4ZHANG Ping4

作者信息

  • 1. School of Nursing , University of South China, Hengyang, Hunan 421001, China
  • 2. Life Science Research Center, University of South China, Hengyang, Hunan 421001, China
  • 3. Department of Infection, Hunan Children's Hospital, Changsha,Hunan 410000, China
  • 4. Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai 200032, China
  • 折叠

摘要

Abstract

Background Macrophage migration inhibitory factor (MIF) is an upstream regulator in immune and inflammatory responses.However,its role in viral myocarditis remains unknown.In this study,we investigated the role of the MIF in coxsackievirus B3 (CVB3)-induced myocarditis.Methods Mice were randomized into two groups receiving either Eagle's minimal essential medium (EMEM,control group) or virus solution (infected group).Subsets of mice in the infected group were sacrificed on days 3,7,14 and 28 after inoculation.Expression of MIF was detected using an enzyme-linked immunosorbent assay (ELISA),reverse transcription polymerase chain reaction and immunohistochemistry.A neutralizing antibody (Ab) to MIF was injected intraperitoneally from day 0 to 7 after inoculation.Disease severity was estimated by histopathology of the heart and by the heart weight to body weight ratio,and the interleukin-1β (IL-1β) and tumor necrosis factor α (TNF-α) in the myocardium were measured by ELISA on day 14.Results The serum MIF concentration and expression levels of myocardial MIF mRNA and protein were significantly elevated in mice on days 7 and 14 post-infection.The survival rate was markedly higher and disease severity was obviously less in mice treated with anti-MIF Ab.Furthermore,MIF blockade significantly decreased the IL-1β and TNF-α in the myocarditic heart.Conclusion These results demonstrate that MIF is an important naturally occurring inflammatory cytokine in CVB3-induced myocarditis,and anti-MIF Ab may lessen the inflammatory response.

关键词

myocarditis/coxsackievirus B3/macrophage migration inhibitory factor/interleukin- 1 β/tumor necrosis factor-a/inflammation

Key words

myocarditis/coxsackievirus B3/macrophage migration inhibitory factor/interleukin- 1 β/tumor necrosis factor-a/inflammation

引用本文复制引用

YU Xiao-hua,LI Shuang-jie,CHEN Rui-zhen,YANG Ying-zhen,ZHANG Ping..Pathogenesis of coxsackievirus B3-induced myocarditis: role of macrophage migration inhibitory factor[J].中华医学杂志(英文版),2012,125(1):50-55,6.

基金项目

This stuay was supported by the grants trom the National Natural Science Foundation of China (No.30271665),and the Plan Project of Hunan Provincial Science & Technology Department of China (No.2009JT4010). (No.30271665)

中华医学杂志(英文版)

OACSCDCSTPCDMEDLINESCI

0366-6999

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