Flavivirus Entry Inhibitors

被引:25
作者
Wang, Qing-Yin [1 ]
Shi, Pei-Yong [1 ]
机构
[1] Novartis Inst Trop Dis, 10 Biopolis Rd,Chromos Bldg, Singapore 138670, Singapore
关键词
flavivirus; virus entry; antivirals; DENGUE VIRUS-INFECTION; BORNE ENCEPHALITIS-VIRUS; ENVELOPE PROTEIN; CRYSTAL-STRUCTURE; JAPANESE ENCEPHALITIS; YELLOW-FEVER; DOMAIN-III; IN-VITRO; SULFATED POLYSACCHARIDE; PEPTIDE INHIBITORS;
D O I
10.1021/acsinfecdis.5b00066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Many flaviviruses are significant human pathogens that are transmitted by mosquitoes and ticks. Although effective vaccines are available for yellow fever virus, Japanese encephalitic virus, and tick-borne encephalitis virus, these and other flaviviruses still cause thousands of human deaths and millions of illnesses each year. No clinically approved antiviral therapy is available for flavivirus treatment. To meet this unmet medical need, industry and academia have taken multiple approaches to develop antiflavivirus therapy, among which targeting viral entry has been actively pursued in the past decade. Here we review the current knowledge of flavivirus entry and its use for small molecule drug discovery. Inhibitors of two major steps of flaviviral entry have been reported: (i) molecules that block virus-receptor interaction; (ii) compounds that prevent conformational change of viral envelope protein during virus-host membrane fusion. We also discuss the advantages and disadvantages of targeting viral entry for treatment of flavivirus infection as compared to targeting viral replication proteins.
引用
收藏
页码:428 / 434
页数:7
相关论文
共 75 条
[41]   A ligand-binding pocket in the dengue virus envelope glycoprotein [J].
Modis, Y ;
Ogata, S ;
Clements, D ;
Harrison, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) :6986-6991
[42]   Variable surface epitopes in the crystal structure of dengue virus type 3 envelope glycoprotein [J].
Modis, Y ;
Ogata, S ;
Clements, D ;
Harrison, SC .
JOURNAL OF VIROLOGY, 2005, 79 (02) :1223-1231
[43]   Structure of the dengue virus envelope protein after membrane fusion [J].
Modis, Y ;
Ogata, S ;
Clements, D ;
Harrison, SC .
NATURE, 2004, 427 (6972) :313-319
[44]  
Modis Y, 2013, ADV EXP MED BIOL, V790, P150, DOI 10.1007/978-1-4614-7651-1_8
[45]   New Insights into Flavivirus Evolution, Taxonomy and Biogeographic History, Extended by Analysis of Canonical and Alternative Coding Sequences [J].
Moureau, Gregory ;
Cook, Shelley ;
Lemey, Philippe ;
Nougairede, Antoine ;
Forrester, Naomi L. ;
Khasnatinov, Maxim ;
Charrel, Remi N. ;
Firth, Andrew E. ;
Gould, Ernest A. ;
de lamballerie, Xavier .
PLOS ONE, 2015, 10 (02)
[46]   A structural perspective of the Flavivirus life cycle [J].
Mukhopadhyay, S ;
Kuhn, RJ ;
Rossmann, MG .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (01) :13-22
[47]   Inhibition of interferon signaling by dengue virus [J].
Muñoz-Jordán, JL ;
Sánchez-Burgos, GG ;
Laurent-Rolle, M ;
García-Sastre, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :14333-14338
[48]   Dendritic-cell-specific ICAM3-grabbing non-integrin is essential for the productive infection of human dendritic cells by mosquito-cell-derived dengue viruses [J].
Navarro-Sanchez, E ;
Altmeyer, R ;
Amara, A ;
Schwartz, O ;
Fieschi, F ;
Virelizier, JL ;
Arenzana-Seisdedos, F ;
Desprès, P .
EMBO REPORTS, 2003, 4 (07) :723-728
[49]   Viral entry inhibitors block dengue antibody-dependent enhancement in vitro [J].
Nicholson, Cindo O. ;
Costin, Joshua M. ;
Rowe, Dawne K. ;
Lin, Li ;
Jenwitheesuk, Ekachai ;
Samudrala, Ram ;
Isern, Sharon ;
Michael, Scott F. .
ANTIVIRAL RESEARCH, 2011, 89 (01) :71-74
[50]   Structural basis of West Nile virus neutralization by a therapeutic antibody [J].
Nybakken, GE ;
Oliphant, T ;
Johnson, S ;
Burke, S ;
Diamond, MS ;
Fremont, DH .
NATURE, 2005, 437 (7059) :764-768