4.7 Article

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

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SCIENTIFIC REPORTS
卷 4, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep05344

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资金

  1. JSPS KAKENHI Grant [25304045, 25660229, 23658243]
  2. Japan Society for the Promotion of Science
  3. Health and Labour Sciences Research Grant on Emerging and Re-emerging Infectious Diseases from the Japanese Ministry of Health, Labour and Welfare
  4. Research on International Cooperation in Medical Science (Japan-US Cooperative Program), Health and Labour Sciences Research Grants
  5. Cooperative Research Grant(s) of NEKKEN
  6. Japan Initiative for Global Research Network on Infectious Diseases
  7. Grants-in-Aid for Scientific Research [25304045, 25660229, 23658243] Funding Source: KAKEN

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Tick-borne encephalitis virus (TBEV) causes acute central nervous system disease. Here, we investigated the roles of the TNF-alpha, 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-alpha KO and IL-10 KO mice compared with wild type (WT) mice. These results suggested that TNF-alpha 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-alpha KO and IL-10 KO mice were not significantly different compared with those of WT mice. On the other hand, all WT, TNF-alpha 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-alpha, IL-10 and IL-2 are key factors for disease remission from fatal encephalitis due to infection with Oshima strain of TBEV.

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