4.7 Article

Enforced viral replication activates adaptive immunity and is essential for the control of a cytopathic virus

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NATURE IMMUNOLOGY
卷 13, 期 1, 页码 51-U131

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NATURE PUBLISHING GROUP
DOI: 10.1038/ni.2169

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资金

  1. Alexander von Humboldt Foundation [SKA-2008, SKA-2010]
  2. Collaborative Research Center [SFB575]
  3. Deutsche Forschungsgemeinschaft [LA1419/3-1, SFB-TR19, FOR729]
  4. MOI Manchot Graduate School (Jurgen Manchot Foundation)
  5. Swiss National Science Foundation [PASMP3-127678/1]
  6. US National Institutes of Health [R01 HL091549]
  7. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL091549] Funding Source: NIH RePORTER
  8. Grants-in-Aid for Scientific Research [23390095] Funding Source: KAKEN

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The innate immune system limits viral replication via type I interferon and also induces the presentation of viral antigens to cells of the adaptive immune response. Using infection of mice with vesicular stomatitis virus, we analyzed how the innate immune system inhibits viral propagation but still allows the presentation of antigen to cells of the adaptive immune response. We found that expression of the gene encoding the inhibitory protein Usp18 in metallophilic macrophages led to lower type I interferon responsiveness, thereby allowing locally restricted replication of virus. This was essential for the induction of adaptive antiviral immune responses and, therefore, for preventing the fatal outcome of infection. In conclusion, we found that enforced viral replication in marginal zone macrophages was an immunological mechanism that ensured the production of sufficient antigen for effective activation of the adaptive immune response.

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