Activation of human monocytes after infection by human coronavirus 229E

被引:78
作者
Desforges, Marc [1 ]
Miletti, Tina C. [1 ]
Gagnon, Mylene [1 ]
Talbot, Pierre J. [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
human coronavirus; monocytes; THP-1; activation; cytokines; chemokines;
D O I
10.1016/j.virusres.2007.06.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human coronaviruses (HCoV) are recognized respiratory pathogens that may be involved in other pathologies such as central nervous system (CNS) diseases. To investigate whether leukocytes could participate in respiratory pathologies and serve as vector for viral spread towards other tissues, the susceptibility of human leukocytic cell lines and peripheral blood mononuclear cells (PBMC) to HCoV-229E and HCoV-OC43 infection was investigated. Human primary monocytes/macrophages were susceptible to HCoV-229E infection, but strongly restricted HCov-OC43 replication. Moreover, productive HCoV-229E infection of primary monocytes and of the THP-1 monocytic cell line led to their activation, as indicated by the production of pro-inflammatory mediators, including TNF-alpha, CCL5, CXCL10 and CXCL11 and MMP-9. Moreover, an in vitro chemotaxis assay showed that motility towards chemokines of THP-1 cells and primary monocytes was increased following an acute or persistent HCoV-229E infection. Taken together, these results suggest that infected monocytes could serve as a reservoir for HCoV-229E, become activated, participate in the exacerbation of pulmonary pathologies, as well as serve as potential vectors for viral dissemination to host tissues, where it could be associated with other pathologies. (c) 2007 Elsevier B.V. All riahts reserved.
引用
收藏
页码:228 / 240
页数:13
相关论文
共 76 条
[1]   Virus attachment and entry offer numerous targets for antiviral therapy [J].
Altmeyer, R .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (30) :3701-3712
[2]   Neuroinvasion by human respiratory coronaviruses [J].
Arbour, N ;
Day, R ;
Newcombe, J ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 2000, 74 (19) :8913-8921
[3]  
ASHMUN RA, 1990, BLOOD, V75, P462
[4]   Analyses of all matrix metalloproteinase members in leukocytes emphasize monocytes as major inflammatory mediators in multiple sclerosis [J].
Bar-Or, A ;
Nuttall, RK ;
Duddy, M ;
Alter, A ;
Kim, HJ ;
Ifergan, I ;
Pennington, CJ ;
Bourgoin, P ;
Edwards, DR ;
Yong, VW .
BRAIN, 2003, 126 :2738-2749
[5]   A role for CXCL12 (SDF-1α) in the pathogenesis of multiple sclerosis:: Regulation of CXCL12 expression in astrocytes by soluble myelin basic protein [J].
Calderon, Tina M. ;
Eugenin, Eliseo A. ;
Lopez, Lillie ;
Kumar, Sridhar Sampath ;
Hesselgesser, Joseph ;
Raine, Cedric S. ;
Berman, Joan W. .
JOURNAL OF NEUROIMMUNOLOGY, 2006, 177 (1-2) :27-39
[6]   Chemokine receptors in the central nervous system: role in brain inflammation and neurodegenerative diseases [J].
Cartier, L ;
Hartley, O ;
Dubois-Dauphin, M ;
Krause, KH .
BRAIN RESEARCH REVIEWS, 2005, 48 (01) :16-42
[7]   MONOCYTES AND MACROPHAGES - FUNCTIONS AND DISEASES [J].
CLINE, MJ ;
LEHRER, RI ;
TERRITO, MC ;
GOLDE, DW .
ANNALS OF INTERNAL MEDICINE, 1978, 88 (01) :78-88
[8]   In vitro detection of apoptosis in monocytes/macrophages infected with human coronavirus [J].
Collins, AR .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2002, 9 (06) :1392-1395
[9]  
Collins AR, 1998, ADV EXP MED BIOL, V440, P635
[10]   Cytokine induction by the hepatitis B virus capsid in macrophages is facilitated by membrane heparan sulfate and involves TLR2 [J].
Cooper, A ;
Tal, G ;
Lider, O ;
Shaul, Y .
JOURNAL OF IMMUNOLOGY, 2005, 175 (05) :3165-3176