EBV-encoded dUTPase induces immune dysregulation: Implications for the pathophysiology of EBV-associated disease

被引:80
作者
Glaser, R
Litsky, ML
Padgett, DA
Baiocchi, RA
Yang, EV
Chen, M
Yeh, PE
Green-Church, KB
Caligiuri, MA
Williams, MV
机构
[1] Ohio State Univ, Inst Behav Med Res, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Oral Biol, Columbus, OH 43210 USA
[5] Ohio State Univ, Med Ctr, Dept Internal Med, Columbus, OH 43210 USA
[6] Ohio State Univ, Mass Spectrometry & Proteom Facil, Columbus, OH 43210 USA
关键词
monocytes/macrophages; Epstein-Barr virus; cytokines; tumor immunity; cancer;
D O I
10.1016/j.virol.2005.10.034
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Epstein-Barr virus (EBV) encodes for several enzymes that are involved in viral DNA replication. There is evidence that some viral proteins, by themselves, call induce immune dysregulation that may contribute to the pathophysiology of the virus infection. In this study, we focused oil the EBV-encoded deoxyuridine triphosphate nucleotidohydrolase (dUTPase) and present the first evidence that the dUTPase is able to induce immune dysregulation in vitro as demonstrated by the inhibition of the replication of stimulated peripheral blood mononuclear cells (PBMCs) and the upregulation of several proinflammatory cytokines including TNF-alpha, IL-1 beta, IL-8, IL-6, and IL-10 produced by unstimulated PBMCs treated with purified EBV-encoded dUTPase. Depletion of CD14-positive cells (monocytes) eliminated the cytokine profile induced by EBV dUTPase treatment. The data support the hypothesis that at least one protein of the EBV early antigen complex can induce immune dysregulation and may be involved in the pathophysiology of EBV-associated disease. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:205 / 218
页数:14
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