Cargando…

A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice

For prevention of HIV infection many currently licensed anti-HIV drugs and new ones in the pipeline show potential as topically applied microbicides. While macaque models have been the gold standard for in vivo microbicide testing, they are expensive and sufficient numbers are not available. Therefo...

Descripción completa

Detalles Bibliográficos
Autores principales: Neff, C. Preston, Kurisu, Theresa, Ndolo, Thomas, Fox, Kami, Akkina, Ramesh
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105981/
https://www.ncbi.nlm.nih.gov/pubmed/21673796
http://dx.doi.org/10.1371/journal.pone.0020209
_version_ 1782204748478283776
author Neff, C. Preston
Kurisu, Theresa
Ndolo, Thomas
Fox, Kami
Akkina, Ramesh
author_facet Neff, C. Preston
Kurisu, Theresa
Ndolo, Thomas
Fox, Kami
Akkina, Ramesh
author_sort Neff, C. Preston
collection PubMed
description For prevention of HIV infection many currently licensed anti-HIV drugs and new ones in the pipeline show potential as topically applied microbicides. While macaque models have been the gold standard for in vivo microbicide testing, they are expensive and sufficient numbers are not available. Therefore, a small animal model that facilitates rapid evaluation of potential candidates for their preliminary efficacy is urgently needed in the microbicide field. We previously demonstrated that RAG-hu humanized mouse model permits HIV-1 mucosal transmission via both vaginal and rectal routes and that oral pre-exposure chemo-prophylactic strategies could be tested in this system. Here in these proof-of-concept studies, we extended this system for topical microbicide testing using HIV-1 as the challenge virus. Maraviroc, a clinically approved CCR5 inhibitor drug for HIV treatment, was formulated as a microbicide gel at 5 mM concentration in 2.2% hydroxyl ethyl cellulose. Female RAG-hu mice were challenged vaginally with HIV-1 an hour after intravaginal application of the maraviroc gel. Our results showed that maraviroc gel treated mice were fully protected against vaginal HIV-1 challenge in contrast to placebo gel treated mice which all became infected. These findings highlight the utility of the humanized mouse models for microbicide testing and, together with the recent data from macaque studies, suggest that maraviroc is a promising candidate for future microbicide clinical trials in the field.
format Text
id pubmed-3105981
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31059812011-06-13 A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice Neff, C. Preston Kurisu, Theresa Ndolo, Thomas Fox, Kami Akkina, Ramesh PLoS One Research Article For prevention of HIV infection many currently licensed anti-HIV drugs and new ones in the pipeline show potential as topically applied microbicides. While macaque models have been the gold standard for in vivo microbicide testing, they are expensive and sufficient numbers are not available. Therefore, a small animal model that facilitates rapid evaluation of potential candidates for their preliminary efficacy is urgently needed in the microbicide field. We previously demonstrated that RAG-hu humanized mouse model permits HIV-1 mucosal transmission via both vaginal and rectal routes and that oral pre-exposure chemo-prophylactic strategies could be tested in this system. Here in these proof-of-concept studies, we extended this system for topical microbicide testing using HIV-1 as the challenge virus. Maraviroc, a clinically approved CCR5 inhibitor drug for HIV treatment, was formulated as a microbicide gel at 5 mM concentration in 2.2% hydroxyl ethyl cellulose. Female RAG-hu mice were challenged vaginally with HIV-1 an hour after intravaginal application of the maraviroc gel. Our results showed that maraviroc gel treated mice were fully protected against vaginal HIV-1 challenge in contrast to placebo gel treated mice which all became infected. These findings highlight the utility of the humanized mouse models for microbicide testing and, together with the recent data from macaque studies, suggest that maraviroc is a promising candidate for future microbicide clinical trials in the field. Public Library of Science 2011-06-01 /pmc/articles/PMC3105981/ /pubmed/21673796 http://dx.doi.org/10.1371/journal.pone.0020209 Text en Neff et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Neff, C. Preston
Kurisu, Theresa
Ndolo, Thomas
Fox, Kami
Akkina, Ramesh
A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title_full A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title_fullStr A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title_full_unstemmed A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title_short A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice
title_sort topical microbicide gel formulation of ccr5 antagonist maraviroc prevents hiv-1 vaginal transmission in humanized rag-hu mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105981/
https://www.ncbi.nlm.nih.gov/pubmed/21673796
http://dx.doi.org/10.1371/journal.pone.0020209
work_keys_str_mv AT neffcpreston atopicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT kurisutheresa atopicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT ndolothomas atopicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT foxkami atopicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT akkinaramesh atopicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT neffcpreston topicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT kurisutheresa topicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT ndolothomas topicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT foxkami topicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice
AT akkinaramesh topicalmicrobicidegelformulationofccr5antagonistmaravirocpreventshiv1vaginaltransmissioninhumanizedraghumice