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Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection
Herpes simplex viruses type 1 (HSV-1) and type 2 (HSV-2) are highly prevalent within the human population and are characterized by lifelong infections and sporadic recurrences due to latent neuron infection. Upon reactivations, HSVs may manifest either, symptomatically or asymptomatically and be she...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026011/ https://www.ncbi.nlm.nih.gov/pubmed/32117158 http://dx.doi.org/10.3389/fmicb.2020.00139 |
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author | Álvarez, Diana M. Castillo, Estefanía Duarte, Luisa F. Arriagada, José Corrales, Nicolás Farías, Mónica A. Henríquez, Adolfo Agurto-Muñoz, Cristian González, Pablo A. |
author_facet | Álvarez, Diana M. Castillo, Estefanía Duarte, Luisa F. Arriagada, José Corrales, Nicolás Farías, Mónica A. Henríquez, Adolfo Agurto-Muñoz, Cristian González, Pablo A. |
author_sort | Álvarez, Diana M. |
collection | PubMed |
description | Herpes simplex viruses type 1 (HSV-1) and type 2 (HSV-2) are highly prevalent within the human population and are characterized by lifelong infections and sporadic recurrences due to latent neuron infection. Upon reactivations, HSVs may manifest either, symptomatically or asymptomatically and be shed onto others through mucosae body fluids. Although, HSVs can produce severe disease in humans, such as life-threatening encephalitis and blindness, the most common symptoms are skin and mucosal lesions in the oro-facial and the genital areas. Nucleoside analogs with antiviral activity can prevent severe HSV infection, yet they are not very effective for treating skin manifestations produced by these viruses, as they only reduce in a few days at most the duration of lesions. Additionally, HSV variants that are resistant to these antivirals may arise, especially in immunosuppressed individuals. Thus, new antivirals that can reduce the severity and duration of these cutaneous manifestations would certainly be welcome. Here, we review currently available anti-herpetic therapies, novel molecules being assessed in clinical trials and new botanical compounds reported in the last 20 years with antiviral activities against HSVs that might represent future treatments against these viruses. |
format | Online Article Text |
id | pubmed-7026011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70260112020-02-28 Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection Álvarez, Diana M. Castillo, Estefanía Duarte, Luisa F. Arriagada, José Corrales, Nicolás Farías, Mónica A. Henríquez, Adolfo Agurto-Muñoz, Cristian González, Pablo A. Front Microbiol Microbiology Herpes simplex viruses type 1 (HSV-1) and type 2 (HSV-2) are highly prevalent within the human population and are characterized by lifelong infections and sporadic recurrences due to latent neuron infection. Upon reactivations, HSVs may manifest either, symptomatically or asymptomatically and be shed onto others through mucosae body fluids. Although, HSVs can produce severe disease in humans, such as life-threatening encephalitis and blindness, the most common symptoms are skin and mucosal lesions in the oro-facial and the genital areas. Nucleoside analogs with antiviral activity can prevent severe HSV infection, yet they are not very effective for treating skin manifestations produced by these viruses, as they only reduce in a few days at most the duration of lesions. Additionally, HSV variants that are resistant to these antivirals may arise, especially in immunosuppressed individuals. Thus, new antivirals that can reduce the severity and duration of these cutaneous manifestations would certainly be welcome. Here, we review currently available anti-herpetic therapies, novel molecules being assessed in clinical trials and new botanical compounds reported in the last 20 years with antiviral activities against HSVs that might represent future treatments against these viruses. Frontiers Media S.A. 2020-02-11 /pmc/articles/PMC7026011/ /pubmed/32117158 http://dx.doi.org/10.3389/fmicb.2020.00139 Text en Copyright © 2020 Álvarez, Castillo, Duarte, Arriagada, Corrales, Farías, Henríquez, Agurto-Muñoz and González. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Álvarez, Diana M. Castillo, Estefanía Duarte, Luisa F. Arriagada, José Corrales, Nicolás Farías, Mónica A. Henríquez, Adolfo Agurto-Muñoz, Cristian González, Pablo A. Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title | Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title_full | Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title_fullStr | Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title_full_unstemmed | Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title_short | Current Antivirals and Novel Botanical Molecules Interfering With Herpes Simplex Virus Infection |
title_sort | current antivirals and novel botanical molecules interfering with herpes simplex virus infection |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026011/ https://www.ncbi.nlm.nih.gov/pubmed/32117158 http://dx.doi.org/10.3389/fmicb.2020.00139 |
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