Transcriptome profile within the mouse central nervous system and activation of myelin-reactive T cells following murine coronavirus infection

被引:11
作者
Gruslin, E [1 ]
Moisan, S [1 ]
St-Pierre, Y [1 ]
Desforges, M [1 ]
Talbot, PJ [1 ]
机构
[1] INRS Inst Armand Frappier, Lab Neuroimmunovirol, Laval, PQ H7V 1B7, Canada
基金
加拿大健康研究院;
关键词
autoimmunity; coronavirus; inflammation; multiple sclerosis; T cells; transcriptome;
D O I
10.1016/j.jneuroim.2005.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is an autoimmune disease associated with environmental factors, possibly including several viruses such as the coronaviruses. Indeed, murine coronavirus (MHV) infection provides a well-known experimental model for MS studies. Intracerebral infection of C57BL/6 mice with MHV-A59 revealed that viral replication was efficient and that clearance of infectious virus occurred as soon as 7 days post-infection. Using cDNA arrays, analysis of gene expression profile in the brain revealed a modulation of 80 different genes following infection, with at least 27 of these genes having previously been directly related to innate or acquired immune responses. Concordingly, an important activation of auto-reactive T cells specific to myelin basic protein was demonstrated. Altogether, these results indicate that an MHV infection of the central nervous system (CNS) leads to an important host genomic response implicating immunity-related genes and to the activation of myelin-reactive autoimmune T cells. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 70
页数:11
相关论文
共 53 条
[1]   Persistent infection of human oligodendrocytic and neuroglial cell lines by human coronavirus 229E [J].
Arbour, N ;
Ekandé, S ;
Côté, G ;
Lachance, C ;
Chagnon, F ;
Tardieu, M ;
Cashman, NR ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 1999, 73 (04) :3326-3337
[2]   Neuroinvasion by human respiratory coronaviruses [J].
Arbour, N ;
Day, R ;
Newcombe, J ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 2000, 74 (19) :8913-8921
[3]   Acute and persistent infection of human neural cell lines by human coronavirus OC43 [J].
Arbour, N ;
Côté, G ;
Lachance, C ;
Tardieu, M ;
Cashman, NR ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 1999, 73 (04) :3338-3350
[4]   THE OLFACTORY NERVE AND NOT THE TRIGEMINAL NERVE IS THE MAJOR SITE OF CNS ENTRY FOR MOUSE HEPATITIS-VIRUS, STRAIN JHM [J].
BARNETT, EM ;
PERLMAN, S .
VIROLOGY, 1993, 194 (01) :185-191
[5]   OLFACTORY NEURAL PATHWAY IN MOUSE HEPATITIS-VIRUS NASOENCEPHALITIS [J].
BARTHOLD, SW .
ACTA NEUROPATHOLOGICA, 1988, 76 (05) :502-506
[6]   Infection of primary cultures of human neural cells by human coronaviruses 229E and OC43 [J].
Bonavia, A ;
Arbour, N ;
Yong, VW ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 1997, 71 (01) :800-806
[7]   2 CORONAVIRUSES ISOLATED FROM CENTRAL NERVOUS-SYSTEM TISSUE OF 2 MULTIPLE-SCLEROSIS PATIENTS [J].
BURKS, JS ;
DEVALD, BL ;
JANKOVSKY, LD ;
GERDES, JC .
SCIENCE, 1980, 209 (4459) :933-934
[8]   B7-H3:: A costimulatory molecule for T cell activation and IFN-γ production [J].
Chapoval, AI ;
Ni, J ;
Lau, JS ;
Wilcox, RA ;
Flies, DB ;
Liu, D ;
Dong, HD ;
Sica, GL ;
Zhu, GF ;
Tamada, K ;
Chen, LP .
NATURE IMMUNOLOGY, 2001, 2 (03) :269-274
[9]   PHYSICOCHEMICAL PROPERTIES OF MURINE HEPATITIS-VIRUS, STRAIN-A59 [J].
DANIEL, C ;
TALBOT, PJ .
ARCHIVES OF VIROLOGY, 1987, 96 (3-4) :241-248
[10]   CENTRAL-NERVOUS-SYSTEM MYELIN - STRUCTURE, FUNCTION, AND PATHOLOGY [J].
DEBER, CM ;
REYNOLDS, SJ .
CLINICAL BIOCHEMISTRY, 1991, 24 (02) :113-134