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

被引:11
作者
Hayashi, Kyoko [1 ]
Onoue, Hiroki [1 ]
Sasaki, Kohei [1 ]
Lee, Jung-Bum [1 ]
Kumar, Penmetcha K. R. [2 ]
Gopinath, Subash C. B. [2 ]
Maitani, Yoshie [3 ]
Kai, Takashi [4 ]
Hayashi, Toshimitsu [1 ]
机构
[1] Toyama Univ, Grad Sch Med & Pharmaceut Sci Res, Toyama 9300194, Japan
[2] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, Tsukuba, Ibaraki 3058566, Japan
[3] Hoshi Univ, Inst Med Chem, Shinagawa Ku, Tokyo 1428501, Japan
[4] Nippon Shokubai Co Ltd, Chiyoda Ku, Tokyo 1000011, Japan
关键词
ACYCLOVIR; INFECTION; TYPE-1; WOMEN; HIV; MEN; INACTIVATION; ACQUISITION; INHIBITOR; COATINGS;
D O I
10.1007/s00705-013-1829-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 (R)), 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.
引用
收藏
页码:425 / 435
页数:11
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