Recognition of viral single-stranded RNA by Toll-like receptors

被引:97
作者
Diebold, Sandra S. [1 ]
机构
[1] Kings Coll London, Guys Hosp, Peter Gorer Dept Immunobiol, London SE1 9RT, England
关键词
adjuvant; dendritic cells; immune response modifiers; innate immunity; pathogen-associated molecular patterns; pattern recognition receptors; Toll-like receptors; virus;
D O I
10.1016/j.addr.2007.11.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Toll-like receptors (TLR), mediating innate immune activation upon recognition of viral nucleic acids, represent promising targets for the development of adjuvants. Therefore, there is great interest in unraveling the underlying mechanisms of ligand recognition. Studies aiming to identify which sequences, nucleic acid modifications and molecular moieties of viral nucleic acids trigger or inhibit TLR activation have allowed insights into this subject, yet there are still many aspects of innate recognition of viral nucleic acids which are only partially understood. This review discusses our current understanding of TLR-mediated recognition of viral single-stranded RNA (ssRNA) by TLR7 and TLR8. Oligoribonucleotides (ORN) and small immune response modifiers such as imidazoquinolines with agonist function have served as tools to study ligand recognition. In addition, there is increasing evidence that TLR-mediated recognition of mammalian ssRNA triggers innate immune activation and plays a role in autoimmunity. Thus the development of suitable TLR7 and TLR8 antagonists could pave the way for therapeutic intervention of particular autoimmune diseases. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:813 / 823
页数:11
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