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Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV
Penile acquisition of HIV infection contributes substantially to the global epidemic. Our goal was to establish a preclinical macaque model of penile HIV infection for evaluating the efficacy of new HIV prevention modalities. Rhesus macaques were challenged once or twice weekly with consistent doses...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870976/ https://www.ncbi.nlm.nih.gov/pubmed/29584769 http://dx.doi.org/10.1371/journal.pone.0194837 |
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author | Garber, David A. Mitchell, James Adams, Debra Guenthner, Patricia Deyounks, Frank Ellis, Shanon Kelley, Kristen Johnson, Ryan Dobard, Charles Heneine, Walid McNicholl, Janet |
author_facet | Garber, David A. Mitchell, James Adams, Debra Guenthner, Patricia Deyounks, Frank Ellis, Shanon Kelley, Kristen Johnson, Ryan Dobard, Charles Heneine, Walid McNicholl, Janet |
author_sort | Garber, David A. |
collection | PubMed |
description | Penile acquisition of HIV infection contributes substantially to the global epidemic. Our goal was to establish a preclinical macaque model of penile HIV infection for evaluating the efficacy of new HIV prevention modalities. Rhesus macaques were challenged once or twice weekly with consistent doses of SHIV(sf)162P3 (a chimeric simian-human immunodeficiency virus containing HIV env) ranging from 4–600 TCID(50) (50% tissue culture infective dose), via two penile routes, until systemic SHIV infection was confirmed. One route exposed the inner foreskin, glans and urethral os to virus following deposition into the prepuce (foreskin) pouch. The second route introduced the virus non-traumatically into the distal urethra only. Single-route challenges resulted in dose-dependent rates of SHIV acquisition informing selection of optimal SHIV dosing. Concurrent SHIV challenges via the prepuce pouch (200 TCID(50)) and urethra (16 TCID(50)) resulted in infection of 100% (10/10) animals following a median of 2.5 virus exposures (range, 1–12). We describe the first rhesus macaque repeat-exposure SHIV challenge model of penile HIV acquisition. Utilization of the model should further our understanding of penile HIV infection and facilitate the development of new HIV prevention strategies for men. |
format | Online Article Text |
id | pubmed-5870976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58709762018-04-06 Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV Garber, David A. Mitchell, James Adams, Debra Guenthner, Patricia Deyounks, Frank Ellis, Shanon Kelley, Kristen Johnson, Ryan Dobard, Charles Heneine, Walid McNicholl, Janet PLoS One Research Article Penile acquisition of HIV infection contributes substantially to the global epidemic. Our goal was to establish a preclinical macaque model of penile HIV infection for evaluating the efficacy of new HIV prevention modalities. Rhesus macaques were challenged once or twice weekly with consistent doses of SHIV(sf)162P3 (a chimeric simian-human immunodeficiency virus containing HIV env) ranging from 4–600 TCID(50) (50% tissue culture infective dose), via two penile routes, until systemic SHIV infection was confirmed. One route exposed the inner foreskin, glans and urethral os to virus following deposition into the prepuce (foreskin) pouch. The second route introduced the virus non-traumatically into the distal urethra only. Single-route challenges resulted in dose-dependent rates of SHIV acquisition informing selection of optimal SHIV dosing. Concurrent SHIV challenges via the prepuce pouch (200 TCID(50)) and urethra (16 TCID(50)) resulted in infection of 100% (10/10) animals following a median of 2.5 virus exposures (range, 1–12). We describe the first rhesus macaque repeat-exposure SHIV challenge model of penile HIV acquisition. Utilization of the model should further our understanding of penile HIV infection and facilitate the development of new HIV prevention strategies for men. Public Library of Science 2018-03-27 /pmc/articles/PMC5870976/ /pubmed/29584769 http://dx.doi.org/10.1371/journal.pone.0194837 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Garber, David A. Mitchell, James Adams, Debra Guenthner, Patricia Deyounks, Frank Ellis, Shanon Kelley, Kristen Johnson, Ryan Dobard, Charles Heneine, Walid McNicholl, Janet Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title | Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title_full | Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title_fullStr | Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title_full_unstemmed | Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title_short | Development of a repeat-exposure penile SHIV infection model in macaques to evaluate biomedical preventions against HIV |
title_sort | development of a repeat-exposure penile shiv infection model in macaques to evaluate biomedical preventions against hiv |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870976/ https://www.ncbi.nlm.nih.gov/pubmed/29584769 http://dx.doi.org/10.1371/journal.pone.0194837 |
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