The Open Microbiology Journal


ISSN: 1874-2858 ― Volume 10, 2016

Toll-Like Receptors and Viruses: Induction of Innate Antiviral Immune Responses



Angeliki Xagorari1, Katerina Chlichlia*, 2
1 Cell and Gene Therapy Laboratory, Dept. of Hematology/BMT, Gen. Hospital G. Papanikolaou, 57010 Exochi, Thes-saloniki, Greece
2 Dept. Molecular Biology and Genetics, Democritus University of Thrace, Dimitras 19, 68100 Alexandroupolis, Greece

Abstract

Induction of antiviral innate immune responses depends on a family of innate immune receptors, the Toll-like receptors (TLR). TLR mediate the antiviral immune responses by recognizing virus infection, activating signaling pathways and inducing the production of antiviral cytokines and chemokines. ssRNA and dsRNA viruses can be recognized by TLR7/8 and TLR3, respectively. TLR receptors are also involved in the recognition of viruses containing genomes rich in CpG DNA motifs as well as envelope glycoproteins. Cytoplasmic recognition of dsRNA by RNA helicases such as RIG-I and MDA5 provides another means of recognizing viral nucleic acid. In order to counteract the innate host immune system viruses evolved mechanisms that block recognition and signaling through pattern recognition receptors, such as TLRs and RNA helicases. Recently, TLR agonists represent a promising approach for the treatment of infectious diseases. This review will focus on the current knowledge of TLR-mediated immune responses to several viral infections.

Keywords: Toll-like receptors, TLR, innate immunity, virus, RNA helicases, antiviral immune responses.


Article Information


Identifiers and Pagination:

Year: 2008
Volume: 2
First Page: 49
Last Page: 59
Publisher Id: TOMICROJ-2-49
DOI: 10.2174/1874285800802010049

Article History:

Received Date: 18/4/2008
Revision Received Date: 30/4/2008
Acceptance Date: 2/5/2008
Electronic publication date: 14/5/2008
Collection year: 2008

© Xagorari and Chlichlia; Licensee Bentham Open

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.


* Address correspondence to this author at the Department of Molecular Biology and Genetics, Democritus University of Thrace, Dimitras 19, 68100 Alexandroupolis, Greece; E-mail: achlichl@mbg.duth.gr



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