TY - JOUR
T1 - Topical application of polyethylenimine as a candidate for novel prophylactic therapeutics against genital herpes caused by herpes simplex virus
AU - Hayashi, Kyoko
AU - Onoue, Hiroki
AU - Sasaki, Kohei
AU - Lee, Jung Bum
AU - Kumar, Penmetcha K.R.
AU - Gopinath, Subash C.B.
AU - Maitani, Yoshie
AU - Kai, Takashi
AU - Hayashi, Toshimitsu
N1 - Funding Information:
We appreciate Mr. O. Takahashi for high-magnification fluorescence microphotography. This work was supported by a University of Toyama Grant-in-Aid.
PY - 2014/3
Y1 - 2014/3
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84896706731&partnerID=8YFLogxK
U2 - 10.1007/s00705-013-1829-x
DO - 10.1007/s00705-013-1829-x
M3 - 学術論文
C2 - 24046087
AN - SCOPUS:84896706731
SN - 0304-8608
VL - 159
SP - 425
EP - 435
JO - Archives of Virology
JF - Archives of Virology
IS - 3
ER -