Molecules 2011, 16(1), 221-250; doi:10.3390/molecules16010221

Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy

Institut de Biologie et Chimie des Protéines, UMR 5086, Université de Lyon, IFR 128 BioSciences Gerland-Lyon Sud, 69367 Lyon, France
* Author to whom correspondence should be addressed.
Received: 6 October 2010; in revised form: 16 December 2010 / Accepted: 24 December 2010 / Published: 30 December 2010
(This article belongs to the Special Issue Antivirals)
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Abstract: The entry of enveloped viruses into their host cells involves several successive steps, each one being amenable to therapeutic intervention. Entry inhibitors act by targeting viral and/or cellular components, through either the inhibition of protein-protein interactions within the viral envelope proteins or between viral proteins and host cell receptors, or through the inhibition of protein-lipid interactions. Interestingly, inhibitors that concentrate into/onto the membrane in order to target a protein involved in the entry process, such as arbidol or peptide inhibitors of the human immunodeficiency virus (HIV), could allow the use of doses compatible with therapeutic requirements. The efficacy of these drugs validates entry as a point of intervention in viral life cycles. Strategies based upon small molecule antiviral agents, peptides, proteins or nucleic acids, would most likely prove efficient in multidrug combinations, in order to inhibit several steps of virus life cycle and prevent disease progression.
Keywords: inhibitors; viral entry; enveloped virus

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MDPI and ACS Style

Teissier, E.; Penin, F.; Pécheur, E.-I. Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy. Molecules 2011, 16, 221-250.

AMA Style

Teissier E, Penin F, Pécheur E-I. Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy. Molecules. 2011; 16(1):221-250.

Chicago/Turabian Style

Teissier, Elodie; Penin, François; Pécheur, Eve-Isabelle. 2011. "Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy." Molecules 16, no. 1: 221-250.

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