Novel approaches in anti-arenaviral drug development

被引:23
作者
Lee, Andrew M. [1 ]
Pasquato, Antonella [2 ,3 ]
Kunz, Stefan [2 ,3 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, IMM 6, Viral Immunobiol Lab, La Jolla, CA 92037 USA
[2] Univ Lausanne, CH-1011 Lausanne, Switzerland
[3] Univ Hosp Ctr, Inst Microbiol, CH-1011 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
Arenavirus; Small molecule; Antiviral; Inhibitors; Virus entry; Mechanism; Lassa; LCMV; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; STABLE SIGNAL PEPTIDE; ENVELOPE GLYCOPROTEIN; COMBINATORIAL LIBRARIES; IN-VITRO; CONVERTASE SKI-1/S1P; IMINODIACETIC ACID; ENTRY INHIBITORS; PROTEIN-PROTEIN; CELLULAR ENTRY;
D O I
10.1016/j.virol.2010.11.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hemorrhagic fevers caused by arenaviruses are among the most devastating emerging human diseases. Considering the number of individuals affected, the current lack of a licensed vaccine, and the limited therapeutic options, arenaviruses are arguably among the most neglected tropical pathogens and the development of efficacious anti-arenaviral drugs is of high priority. Over the past years significant efforts have been undertaken to identify novel potent inhibitors of arenavirus infection. High throughput screening of small molecule libraries employing pseudotype platforms led to the discovery of several potent and broadly active inhibitors of arenavirus cell entry that are effective against the major hemorrhagic arenaviruses. Mechanistic studies revealed that these novel entry inhibitors block arenavirus membrane fusion and provided novel insights into the unusual mechanism of this process. The success of these approaches highlights the power of small molecule screens in antiviral drug discovery and establishes arenavirus membrane fusion as a robust drug target. These broad screenings have been complemented by strategies targeting cellular factors involved in productive arenavirus infection. Approaches targeting the cellular protease implicated in maturation of the fusion-active viral envelope glycoprotein identified the proteolytic processing of the arenavirus glycoprotein precursor as a novel and promising target for anti-arenaviral strategies. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:163 / 169
页数:7
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