Development of cellular signaling pathway inhibitors as new antivirals against influenza

被引:91
作者
Planz, Oliver [1 ]
机构
[1] Eberhard Karls Univ Tubingen, Interfac Inst Cell Biol, Dept Immunol, D-72076 Tubingen, Germany
关键词
Influenza virus; Antiviral therapy; Cellular drug targets; Signaling pathways; Resistance; NF-KAPPA-B; PROTEIN-KINASE-C; ORAL MEK INHIBITOR; A VIRUS-INFECTION; BRONCHIAL EPITHELIAL-CELLS; PHASE-II; IN-VITRO; NS1; PROTEIN; HEMATOLOGIC MALIGNANCIES; PROTEASOME INHIBITORS;
D O I
10.1016/j.antiviral.2013.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Influenza virus exploits a number of cellular signaling pathways during the course of its replication, rendering them potential targets for new therapeutic interventions. Several preclinical approaches are now focusing on cellular factors or pathways as a means of treating influenza. By targeting host factors, rather than viral mechanisms, these novel therapies may be effective against multiple virus strains and subtypes, and are less likely to elicit viral drug resistance. The most promising candidates are inhibitors of intracellular signaling cascades that are essential for virus replication. This article reviews novel approaches and compounds that target the Raf/MEK/ERK signaling pathway, NF-kappa B signaling, the PI3K/Akt pathway and the PKC signaling cascade. Although these new antiviral strategies are still in an early phase of preclinical development, results to date suggest they offer a new approach to the treatment of influenza, supplementing direct-acting antiviral drugs. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:457 / 468
页数:12
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