Targeting of Toll-like receptors: a decade of progress in combating infectious diseases

被引:110
作者
Hedayat, Mona [1 ,2 ]
Netea, Mihai G. [3 ,4 ]
Rezaei, Nima [1 ,2 ,5 ,6 ]
机构
[1] Univ Tehran Med Sci, Mol Immunol Res Ctr, Sch Med, Tehran, Iran
[2] Univ Tehran Med Sci, Dept Immunol, Sch Med, Tehran, Iran
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med, NL-6525 ED Nijmegen, Netherlands
[4] Nijmegen Inst Infect Inflammat & Immun N4I, Nijmegen, Netherlands
[5] Univ Tehran Med Sci, Res Ctr Immunodeficiencies, Childrens Med Ctr, Pediat Ctr Excellence, Tehran, Iran
[6] Univ Sheffield, Sch Med & Biomed Sci, Dept Infect & Immun, Sheffield, S Yorkshire, England
关键词
HEPATITIS-B-VACCINE; IMIQUIMOD 5-PERCENT CREAM; DOUBLE-STRANDED-RNA; T-CELL RESPONSES; SIGNAL-TRANSDUCTION INHIBITOR; RESIQUIMOD 0.01-PERCENT GEL; EXTRACELLULAR TLR4 DOMAIN; CANDIDATE MALARIA VACCINE; CONTROLLED CLINICAL-TRIAL; MONOPHOSPHORYL-LIPID-A;
D O I
10.1016/S1473-3099(11)70099-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Toll-like receptors (TLRs) recognise highly conserved molecular structures, collectively known as pathogen-associated molecular patterns. In the past two decades, development and clinical implementation of TLR ligands-ie, chemically modified synthetic derivatives of naturally occurring ligands and fully synthetic small molecules-have been topics of intense research. Targeted manipulation of TLR signalling has been applied clinically to boost vaccine effectiveness, promote a robust T helper 1-predominant immune response against viral infection, or dampen the exaggerated inflammatory response to bacterial infection. Use of these new therapeutic molecules as adjuncts to conventional pharmacotherapy or stand-alone treatments might offer solutions to unmet clinical needs or could replace existing partly effective therapeutic strategies. © 2011 Elsevier Ltd.
引用
收藏
页码:702 / 712
页数:11
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