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Prevention of vaginal and rectal herpes simplex virus type 2 transmission in mice: mechanism of antiviral action
R. Ceña-Diez, E. Vacas-Córdoba, P. García-Broncano, FJ. de la Mata, R. Gómez, M. Maly, MÁ. Muñoz-Fernández,
Jazyk angličtina Země Nový Zéland
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2012-01-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2009-01-01
Taylor & Francis Open Access
od 2006-09-01
Medline Complete (EBSCOhost)
od 2012-01-01
Health & Medicine (ProQuest)
od 2012-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
PubMed
27274240
DOI
10.2147/ijn.s95301
Knihovny.cz E-zdroje
- MeSH
- acyklovir farmakologie MeSH
- antiinfekční látky farmakologie MeSH
- antivirové látky farmakologie MeSH
- aplikace rektální MeSH
- Cercopithecus aethiops MeSH
- dendrimery chemie MeSH
- epitelové buňky účinky léků virologie MeSH
- herpes simplex MeSH
- koncentrace vodíkových iontů MeSH
- lidé MeSH
- lidský herpesvirus 2 účinky léků MeSH
- molekulární modely MeSH
- myši inbrední BALB C MeSH
- polymery chemie MeSH
- rektum účinky léků virologie MeSH
- silany chemie MeSH
- tenofovir farmakologie MeSH
- vagina účinky léků virologie MeSH
- Vero buňky MeSH
- virové proteiny metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Topical microbicides to stop sexually transmitted diseases, such as herpes simplex virus type 2 (HSV-2), are urgently needed. The emerging field of nanotechnology offers novel suitable tools for addressing this challenge. Our objective was to study, in vitro and in vivo, antiherpetic effect and antiviral mechanisms of several polyanionic carbosilane dendrimers with anti-HIV-1 activity to establish new potential microbicide candidates against sexually transmitted diseases. Plaque reduction assay on Vero cells proved that G2-S16, G1-S4, and G3-S16 are the dendrimers with the highest inhibitory response against HSV-2 infection. We also demonstrated that our dendrimers inhibit viral infection at the first steps of HSV-2 lifecycle: binding/entry-mediated events. G1-S4 and G3-S16 bind directly on the HSV-2, inactivating it, whereas G2-S16 adheres to host cell-surface proteins. Molecular modeling showed that G1-S4 binds better at binding sites on gB surface than G2-S16. Significantly better binding properties of G1-S4 than G2-S16 were found in an important position for affecting transition of gB trimer from G1-S4 prefusion to final postfusion state and in several positions where G1-S4 could interfere with gB/gH-gL interaction. We demonstrated that these polyanionic carbosilan dendrimers have a synergistic activity with acyclovir and tenofovir against HSV-2, in vitro. Topical vaginal or rectal administration of G1-S4 or G2-S16 prevents HSV-2 transmission in BALB/c mice in values close to 100%. This research represents the first demonstration that transmission of HSV-2 can be blocked by vaginal/rectal application of G1-S4 or G2-S16, providing a step forward to prevent HSV-2 transmission in humans.
Citace poskytuje Crossref.org
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