Topical application of polyethylenimine as a candidate for novel prophylactic therapeutics against genital herpes caused by herpes simplex virus

Herpes simplex virus types 1 (HSV-1) and 2 (HSV-2) cause genital herpes, which can enhance the acquisition of human immunodeficiency virus. The development of anti-HSV agents with novel mechanisms of action is urgently required in the topical therapy of genital herpes. In this study, the in vitro an...

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Veröffentlicht in:Archives of virology 2014-03, Vol.159 (3), p.425-435
Hauptverfasser: Hayashi, Kyoko, Onoue, Hiroki, Sasaki, Kohei, Lee, Jung-Bum, Kumar, Penmetcha K. R, Gopinath, Subash C. B, Maitani, Yoshie, Kai, Takashi, Hayashi, Toshimitsu
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container_title Archives of virology
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creator Hayashi, Kyoko
Onoue, Hiroki
Sasaki, Kohei
Lee, Jung-Bum
Kumar, Penmetcha K. R
Gopinath, Subash C. B
Maitani, Yoshie
Kai, Takashi
Hayashi, Toshimitsu
description Herpes simplex virus types 1 (HSV-1) and 2 (HSV-2) cause genital herpes, which can enhance the acquisition of human immunodeficiency virus. The development of anti-HSV agents with novel mechanisms of action is urgently required in the topical therapy of genital herpes. In this study, the in vitro and in vivo anti-HSV effects of Epomin SP-012®, a highly cationic polyethylenimine, were evaluated. When the in vitro antiviral effects of SP-012 were assessed, this compound showed potent activity against HSV-1 and HSV-2. It inhibited the attachment of HSV-2 to host cells and cell-to-cell spread of infection in a concentration-dependent manner and exerted a virucidal effect. No SP-012-resistant HSV-2 was found when the virus was successively passaged in the presence of SP-012. In a mouse genital herpes model, topically administered SP-012 inhibited the progression of the disease caused by HSV infection. These data illustrate that SP-012 may be a novel class of HSV inhibitor that would be acceptable for long-term topical application.
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In this study, the in vitro and in vivo anti-HSV effects of Epomin SP-012®, a highly cationic polyethylenimine, were evaluated. When the in vitro antiviral effects of SP-012 were assessed, this compound showed potent activity against HSV-1 and HSV-2. It inhibited the attachment of HSV-2 to host cells and cell-to-cell spread of infection in a concentration-dependent manner and exerted a virucidal effect. No SP-012-resistant HSV-2 was found when the virus was successively passaged in the presence of SP-012. In a mouse genital herpes model, topically administered SP-012 inhibited the progression of the disease caused by HSV infection. These data illustrate that SP-012 may be a novel class of HSV inhibitor that would be acceptable for long-term topical application.</abstract><cop>Vienna</cop><pub>Springer-Verlag</pub><pmid>24046087</pmid><doi>10.1007/s00705-013-1829-x</doi><tpages>11</tpages></addata></record>
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subjects Administration, Topical
Animals
Anti-Infective Agents, Local - pharmacology
Anti-Infective Agents, Local - therapeutic use
antiviral properties
Biomedical and Life Sciences
Biomedicine
Cytotoxicity
disease course
Disease Models, Animal
Female
Glycoproteins
Herpes Genitalis - prevention & control
herpes simplex
Herpes simplex virus 1
Herpes simplex virus 2
Herpes viruses
Herpesvirus 1, Human - drug effects
Herpesvirus 1, Human - physiology
Herpesvirus 2, Human - drug effects
Herpesvirus 2, Human - physiology
Human immunodeficiency virus
Human immunodeficiency virus 1
Human immunodeficiency virus 2
Infections
Infectious Diseases
Medical Microbiology
Mice
Mice, Inbred BALB C
Microbial Sensitivity Tests
Microbial Viability - drug effects
Original Article
Polyethyleneimine - pharmacology
Polyethyleneimine - therapeutic use
therapeutics
topical application
Treatment Outcome
Virology
Virus Internalization - drug effects
viruses
title Topical application of polyethylenimine as a candidate for novel prophylactic therapeutics against genital herpes caused by herpes simplex virus
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