Crosstalk between Cytoplasmic RIG-I and STING Sensing Pathways

Alessandra Zevini, David Olagnier, John Hiscottt*

*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperReviewResearchpeer-review

278 Citations (Scopus)

Abstract

Detection of evolutionarily conserved molecules on microbial pathogens by host immune sensors represents the initial trigger of the immune response against infection. Cytosolic receptors sense viral and intracellular bacterial genomes, as well as nucleic acids produced during replication. Once activated, these sensors trigger multiple signaling cascades, converging on the production of type I interferons and proinflammatory cytokines. Although distinct classes of receptors are responsible for the RNA and DNA sensing, the downstream signaling components are physically and functionally interconnected. This review highlights the importance of the crosstalk between retinoic acid inducible gene-I (RIG-I)-mitochondrial antiviral-signaling protein (MAVS) RNA sensing and the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) DNA sensing pathways in potentiating efficient antiviral responses. The potential of cGAS-STING manipulation as a component of cancer immunotherapy is also reviewed.

Original languageEnglish
JournalTrends in Immunology
Volume38
Issue3
Pages (from-to)194-205
Number of pages12
ISSN1471-4906
DOIs
Publication statusPublished - Mar 2017

Keywords

  • GMP-AMP SYNTHASE
  • DEPENDENT INNATE IMMUNITY
  • CYTOSOLIC DNA SENSOR
  • CYCLIC DI-GMP
  • INTERFERON RESPONSE
  • ANTIVIRAL RESPONSE
  • IMMUNOGENIC TUMORS
  • INTRACELLULAR DNA
  • MELANOMA-CELLS
  • CUTTING EDGE

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