Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.

Virus infection is sensed by the innate immune system which then rapidly initiates biosynthesis of type I interferon (IFN). The IFN signaling systems produce a broadly effective innate antiviral response by creating an antiviral state in both an autocrine and paracrine manner in cells and by activat...

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Main Authors: Seeds, R, Gordon, S, Miller, J
Format: Conference item
Udgivet: 2006
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author Seeds, R
Gordon, S
Miller, J
author_facet Seeds, R
Gordon, S
Miller, J
author_sort Seeds, R
collection OXFORD
description Virus infection is sensed by the innate immune system which then rapidly initiates biosynthesis of type I interferon (IFN). The IFN signaling systems produce a broadly effective innate antiviral response by creating an antiviral state in both an autocrine and paracrine manner in cells and by activating innate and adaptive immunity. Plasmacytoid dendritic cells (pDCs) have the unique ability to produce very high levels of type I IFN following viral infection in vivo. Most recent research has focused on oligonucleotide-mediated induction of type I IFN production, implicating viral genome and replication intermediates as the stimulus for this response. However there are additional viral ligands which can potentially induce type I IFN production in pDCs, such as envelope glycoproteins, viral glycolipids, tegument, capsid or nuclear proteins. This area of viral immunology, which has been neglected in the literature, will be discussed here.
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spelling oxford-uuid:056fa29b-cf65-4ccd-b853-0bf8f15156562022-03-26T08:57:06ZReceptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.Conference itemhttp://purl.org/coar/resource_type/c_5794uuid:056fa29b-cf65-4ccd-b853-0bf8f1515656Symplectic Elements at Oxford2006Seeds, RGordon, SMiller, JVirus infection is sensed by the innate immune system which then rapidly initiates biosynthesis of type I interferon (IFN). The IFN signaling systems produce a broadly effective innate antiviral response by creating an antiviral state in both an autocrine and paracrine manner in cells and by activating innate and adaptive immunity. Plasmacytoid dendritic cells (pDCs) have the unique ability to produce very high levels of type I IFN following viral infection in vivo. Most recent research has focused on oligonucleotide-mediated induction of type I IFN production, implicating viral genome and replication intermediates as the stimulus for this response. However there are additional viral ligands which can potentially induce type I IFN production in pDCs, such as envelope glycoproteins, viral glycolipids, tegument, capsid or nuclear proteins. This area of viral immunology, which has been neglected in the literature, will be discussed here.
spellingShingle Seeds, R
Gordon, S
Miller, J
Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title_full Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title_fullStr Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title_full_unstemmed Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title_short Receptors and ligands involved in viral induction of type I interferon production by plasmacytoid dendritic cells.
title_sort receptors and ligands involved in viral induction of type i interferon production by plasmacytoid dendritic cells
work_keys_str_mv AT seedsr receptorsandligandsinvolvedinviralinductionoftypeiinterferonproductionbyplasmacytoiddendriticcells
AT gordons receptorsandligandsinvolvedinviralinductionoftypeiinterferonproductionbyplasmacytoiddendriticcells
AT millerj receptorsandligandsinvolvedinviralinductionoftypeiinterferonproductionbyplasmacytoiddendriticcells