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Learning from the Messengers: Innate Sensing of Viruses and Cytokine Regulation of Immunity-Clues for Treatments and Vaccines

期刊

VIRUSES-BASEL
卷 5, 期 2, 页码 470-527

出版社

MDPI
DOI: 10.3390/v5020470

关键词

virus; innate; PRR; inflammation; IFN; cytokine; therapy; ISG; immune-modulatory; antiviral; vaccine; human; TLR; RLR; DNA

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资金

  1. Danish Medical Research Council [271-05-0632]
  2. Lundbeck Foundation
  3. Danish AIDS Foundation
  4. Scandinavian Society for Antimicrobial Chemotherapy
  5. Research Foundation of Aarhus University
  6. Dagmar Marshall Foundation
  7. Aage and Ejnar Danielsens Foundation
  8. Soren Segel & Johanne Wiibroe Segel's Research Fund
  9. Christian X Foundation
  10. Fonden til Laegevidenskabens Fremme
  11. Jacob and Olga Madsen Foundation
  12. Augustinus Foundation

向作者/读者索取更多资源

Virus infections are a major global public health concern, and only via substantial knowledge of virus pathogenesis and antiviral immune responses can we develop and improve medical treatments, and preventive and therapeutic vaccines. Innate immunity and the shaping of efficient early immune responses are essential for control of viral infections. In order to trigger an efficient antiviral defense, the host senses the invading microbe via pattern recognition receptors (PRRs), recognizing distinct conserved pathogen-associated molecular patterns (PAMPs). The innate sensing of the invading virus results in intracellular signal transduction and subsequent production of interferons (IFNs) and proinflammatory cytokines. Cytokines, including IFNs and chemokines, are vital molecules of antiviral defense regulating cell activation, differentiation of cells, and, not least, exerting direct antiviral effects. Cytokines shape and modulate the immune response and IFNs are principle antiviral mediators initiating antiviral response through induction of antiviral proteins. In the present review, I describe and discuss the current knowledge on early virus-host interactions, focusing on early recognition of virus infection and the resulting expression of type I and type III IFNs, proinflammatory cytokines, and intracellular antiviral mediators. In addition, the review elucidates how targeted stimulation of innate sensors, such as toll-like receptors (TLRs) and intracellular RNA and DNA sensors, may be used therapeutically. Moreover, I present and discuss data showing how current antimicrobial therapies, including antibiotics and antiviral medication, may interfere with, or improve, immune response.

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