Protective role of TNF-α, IL-10 and IL-2 in mice infected with the Oshima strain of Tick-borne encephalitis virus

Sci Rep. 2014 Jun 18:4:5344. doi: 10.1038/srep05344.

Abstract

Tick-borne encephalitis virus (TBEV) causes acute central nervous system disease. Here, we investigated the roles of the TNF-α, IL-10 and other cytokines in appropriate KO mice following infection with Oshima and Sofjin strains of TBEV. Following infection with the Oshima strain, mortality rates were significantly increased in TNF-α KO and IL-10 KO mice compared with wild type (WT) mice. These results suggested that TNF-α and IL-10 play protective roles against fatal infection due to Oshima strain infection. However, viral loads and proinflammatory cytokine levels in the brain of TNF-α KO andIL-10 KO mice were not significantly different compared with those of WT mice. On the other hand, all WT, TNF-α KO and IL-10 KO mice died following infection with Sofjin strain. Interestingly, Sofjin-infected mice did not exhibit an up-regulated mRNA level of IL-2 in the spleen in all groups of mice, whereas Oshima-infected mice showed significantly increased level of IL-2 compared with mock-infected mice. From these results, we suggest that TNF-α, IL-10 and IL-2 are key factors for disease remission from fatal encephalitis due to infection with Oshima strain of TBEV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Brain / virology
  • Cells, Cultured
  • Cytokines / genetics
  • Encephalitis Viruses, Tick-Borne / classification
  • Encephalitis Viruses, Tick-Borne / physiology
  • Encephalitis, Tick-Borne / genetics*
  • Encephalitis, Tick-Borne / mortality
  • Encephalitis, Tick-Borne / virology
  • Gene Expression
  • Host-Pathogen Interactions
  • Inflammation Mediators / metabolism
  • Interleukin-10 / genetics*
  • Interleukin-2 / genetics*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protective Agents / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Species Specificity
  • Survival Rate
  • Time Factors
  • Tumor Necrosis Factor-alpha / genetics*
  • Viral Load

Substances

  • Cytokines
  • Inflammation Mediators
  • Interleukin-2
  • Protective Agents
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Interleukin-10