Antiviral applications of Toll-like receptor agonists

被引:54
作者
Horscroft, Nigel J. [1 ]
Pryde, David C. [1 ]
Bright, Helen [1 ]
机构
[1] Pfizer Global R&D, Sandwich CT13 9NJ, Kent, England
关键词
TLR; immune modulation; therapy; virus; DOUBLE-STRANDED-RNA; NF-KAPPA-B; SPECIES-SPECIFIC RECOGNITION; RESPIRATORY SYNCYTIAL VIRUS; INFLUENZA-VIRUS; IMMUNE-RESPONSE; RIG-I; BIOLOGICAL EVALUATION; TECHNOLOGY EVALUATION; MONOCLONAL-ANTIBODY;
D O I
10.1093/jac/dkr588
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In the past, antiviral research has focused mainly on viral targets. As the search for effective and differentiated antiviral therapies continues, cellular targets are becoming more common, bringing with them a variety of challenges and concerns. Toll-like receptors (TLRs) provide a unique mechanism to induce an antiviral state in the host. In this review we introduce TLRs as targets for the pharmaceutical industry, including how they signal and thereby induce an antiviral state through the production of type I interferons. We examine how TLRs are being therapeutically targeted and discuss several clinically precedented agents for which efficacy and safety data are available. We describe some of the chemistries that have been applied to both small molecule and large molecule leads to tune agonist potency, and offer a differentiated safety profile through targeting certain compartments such as the gut or the lung, thereby limiting systemic drug exposure and affecting systemic cytokine levels. The application of low-dose agonists of TLRs as vaccine adjuvants or immunoprotective agents is also presented. Some of the challenges presented by this approach are then discussed, including viral evasion strategies and mechanism-linked inflammatory cytokine induction.
引用
收藏
页码:789 / 801
页数:13
相关论文
共 144 条
[1]  
Abbott P, 2007, Purine derivatives for the treatment of viral or allergic diseases and cancers, Patent No. 2007034173
[2]   Recognition of pathogen-associated molecular patterns by TLR family [J].
Akira, S ;
Hemmi, H .
IMMUNOLOGY LETTERS, 2003, 85 (02) :85-95
[3]   TLR4 agonists as immunomodulatory agents [J].
Alderson, Mark R. ;
McGowan, Patrick ;
Baldridge, Jory R. ;
Probst, Peter .
JOURNAL OF ENDOTOXIN RESEARCH, 2006, 12 (05) :313-319
[4]   Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[5]  
Anadys, AN PHARM REP 3 QUART
[6]   The V proteins of paramyxoviruses bind the IFN-inducible RNA helicase, mda-5, and inhibit its activation of the IFN-β promoter [J].
Andrejeva, J ;
Childs, KS ;
Young, DF ;
Carlos, TS ;
Stock, N ;
Goodbourn, S ;
Randall, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :17264-17269
[7]  
Averett D, 2007, 3 ANN VIR HEP DRUG D
[8]  
Averett D, 2005, Administration of TLR7 ligands and prodrugs thereof for treatment of infection by hepatitis C virus, Patent No. 2005025583
[9]  
Baldridge J, 2006, INFEC DIS, P235
[10]   Dendritic cells respond to influenza virus through TLR7- and PKR-independent pathways [J].
Barchet, W ;
Krug, A ;
Cella, M ;
Newby, C ;
Fischer, JAA ;
Dzionek, A ;
Pekosz, A ;
Colonna, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (01) :236-242