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Algal Lectins as Potential HIV Microbicide Candidates

The development and use of topical microbicides potentially offers an additional strategy to reduce the spread of the Human Immunodeficiency Virus (HIV). Carbohydrate-binding agents (CBAs) that show specificity for high mannose carbohydrates on the surface of the heavily glycosylated envelope of HIV...

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Autores principales: Huskens, Dana, Schols, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407925/
https://www.ncbi.nlm.nih.gov/pubmed/22851920
http://dx.doi.org/10.3390/md10071476
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author Huskens, Dana
Schols, Dominique
author_facet Huskens, Dana
Schols, Dominique
author_sort Huskens, Dana
collection PubMed
description The development and use of topical microbicides potentially offers an additional strategy to reduce the spread of the Human Immunodeficiency Virus (HIV). Carbohydrate-binding agents (CBAs) that show specificity for high mannose carbohydrates on the surface of the heavily glycosylated envelope of HIV are endowed with potent anti-HIV activity. In fact, a number of algal lectins such as cyanovirin-N, microvirin, microcystis viridis lectin, scytovirin, Oscillatoria agardhii agglutinin and griffithsin are considered as potential microbicide candidates to prevent the sexual transmission of HIV through topical applications. They not only inhibit infection of cells by cell-free virus but they can also efficiently prevent virus transmission from virus-infected cells to uninfected CD4(+) target T-lymphocytes and DC-SIGN-directed capture of HIV-1 and transmission to CD4(+) T lymphocytes. This review focuses on the structural properties and carbohydrate specificity of these algal lectins, their antiviral activity against HIV and several other enveloped viruses, their safety profile and viral resistance patterns.
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spelling pubmed-34079252012-07-31 Algal Lectins as Potential HIV Microbicide Candidates Huskens, Dana Schols, Dominique Mar Drugs Review The development and use of topical microbicides potentially offers an additional strategy to reduce the spread of the Human Immunodeficiency Virus (HIV). Carbohydrate-binding agents (CBAs) that show specificity for high mannose carbohydrates on the surface of the heavily glycosylated envelope of HIV are endowed with potent anti-HIV activity. In fact, a number of algal lectins such as cyanovirin-N, microvirin, microcystis viridis lectin, scytovirin, Oscillatoria agardhii agglutinin and griffithsin are considered as potential microbicide candidates to prevent the sexual transmission of HIV through topical applications. They not only inhibit infection of cells by cell-free virus but they can also efficiently prevent virus transmission from virus-infected cells to uninfected CD4(+) target T-lymphocytes and DC-SIGN-directed capture of HIV-1 and transmission to CD4(+) T lymphocytes. This review focuses on the structural properties and carbohydrate specificity of these algal lectins, their antiviral activity against HIV and several other enveloped viruses, their safety profile and viral resistance patterns. MDPI 2012-07-10 /pmc/articles/PMC3407925/ /pubmed/22851920 http://dx.doi.org/10.3390/md10071476 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Huskens, Dana
Schols, Dominique
Algal Lectins as Potential HIV Microbicide Candidates
title Algal Lectins as Potential HIV Microbicide Candidates
title_full Algal Lectins as Potential HIV Microbicide Candidates
title_fullStr Algal Lectins as Potential HIV Microbicide Candidates
title_full_unstemmed Algal Lectins as Potential HIV Microbicide Candidates
title_short Algal Lectins as Potential HIV Microbicide Candidates
title_sort algal lectins as potential hiv microbicide candidates
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407925/
https://www.ncbi.nlm.nih.gov/pubmed/22851920
http://dx.doi.org/10.3390/md10071476
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