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Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir
BACKGROUND: In the absence of an effective vaccine, HIV continues to spread globally, emphasizing the need for novel strategies to limit its transmission. Pre-exposure prophylaxis (PrEP) with antiretroviral drugs could prove to be an effective intervention strategy if highly efficacious and cost-eff...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2225435/ https://www.ncbi.nlm.nih.gov/pubmed/18254653 http://dx.doi.org/10.1371/journal.pmed.0050028 |
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author | García-Lerma, J. Gerardo Otten, Ron A Qari, Shoukat H Jackson, Eddie Cong, Mian-er Masciotra, Silvina Luo, Wei Kim, Caryn Adams, Debra R Monsour, Michael Lipscomb, Jonathan Johnson, Jeffrey A Delinsky, David Schinazi, Raymond F Janssen, Robert Folks, Thomas M Heneine, Walid |
author_facet | García-Lerma, J. Gerardo Otten, Ron A Qari, Shoukat H Jackson, Eddie Cong, Mian-er Masciotra, Silvina Luo, Wei Kim, Caryn Adams, Debra R Monsour, Michael Lipscomb, Jonathan Johnson, Jeffrey A Delinsky, David Schinazi, Raymond F Janssen, Robert Folks, Thomas M Heneine, Walid |
author_sort | García-Lerma, J. Gerardo |
collection | PubMed |
description | BACKGROUND: In the absence of an effective vaccine, HIV continues to spread globally, emphasizing the need for novel strategies to limit its transmission. Pre-exposure prophylaxis (PrEP) with antiretroviral drugs could prove to be an effective intervention strategy if highly efficacious and cost-effective PrEP modalities are identified. We evaluated daily and intermittent PrEP regimens of increasing antiviral activity in a macaque model that closely resembles human transmission. METHODS AND FINDINGS: We used a repeat-exposure macaque model with 14 weekly rectal virus challenges. Three drug treatments were given once daily, each to a different group of six rhesus macaques. Group 1 was treated subcutaneously with a human-equivalent dose of emtricitabine (FTC), group 2 received orally the human-equivalent dosing of both FTC and tenofovir-disoproxil fumarate (TDF), and group 3 received subcutaneously a similar dosing of FTC and a higher dose of tenofovir. A fourth group of six rhesus macaques (group 4) received intermittently a PrEP regimen similar to group 3 only 2 h before and 24 h after each weekly virus challenge. Results were compared to 18 control macaques that did not receive any drug treatment. The risk of infection in macaques treated in groups 1 and 2 was 3.8- and 7.8-fold lower than in untreated macaques (p = 0.02 and p = 0.008, respectively). All six macaques in group 3 were protected. Breakthrough infections had blunted acute viremias; drug resistance was seen in two of six animals. All six animals in group 4 that received intermittent PrEP were protected. CONCLUSIONS: This model suggests that single drugs for daily PrEP can be protective but a combination of antiretroviral drugs may be required to increase the level of protection. Short but potent intermittent PrEP can provide protection comparable to that of daily PrEP in this SHIV/macaque model. These findings support PrEP trials for HIV prevention in humans and identify promising PrEP modalities. |
format | Text |
id | pubmed-2225435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22254352008-02-05 Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir García-Lerma, J. Gerardo Otten, Ron A Qari, Shoukat H Jackson, Eddie Cong, Mian-er Masciotra, Silvina Luo, Wei Kim, Caryn Adams, Debra R Monsour, Michael Lipscomb, Jonathan Johnson, Jeffrey A Delinsky, David Schinazi, Raymond F Janssen, Robert Folks, Thomas M Heneine, Walid PLoS Med Research Article BACKGROUND: In the absence of an effective vaccine, HIV continues to spread globally, emphasizing the need for novel strategies to limit its transmission. Pre-exposure prophylaxis (PrEP) with antiretroviral drugs could prove to be an effective intervention strategy if highly efficacious and cost-effective PrEP modalities are identified. We evaluated daily and intermittent PrEP regimens of increasing antiviral activity in a macaque model that closely resembles human transmission. METHODS AND FINDINGS: We used a repeat-exposure macaque model with 14 weekly rectal virus challenges. Three drug treatments were given once daily, each to a different group of six rhesus macaques. Group 1 was treated subcutaneously with a human-equivalent dose of emtricitabine (FTC), group 2 received orally the human-equivalent dosing of both FTC and tenofovir-disoproxil fumarate (TDF), and group 3 received subcutaneously a similar dosing of FTC and a higher dose of tenofovir. A fourth group of six rhesus macaques (group 4) received intermittently a PrEP regimen similar to group 3 only 2 h before and 24 h after each weekly virus challenge. Results were compared to 18 control macaques that did not receive any drug treatment. The risk of infection in macaques treated in groups 1 and 2 was 3.8- and 7.8-fold lower than in untreated macaques (p = 0.02 and p = 0.008, respectively). All six macaques in group 3 were protected. Breakthrough infections had blunted acute viremias; drug resistance was seen in two of six animals. All six animals in group 4 that received intermittent PrEP were protected. CONCLUSIONS: This model suggests that single drugs for daily PrEP can be protective but a combination of antiretroviral drugs may be required to increase the level of protection. Short but potent intermittent PrEP can provide protection comparable to that of daily PrEP in this SHIV/macaque model. These findings support PrEP trials for HIV prevention in humans and identify promising PrEP modalities. Public Library of Science 2008-02 2008-02-05 /pmc/articles/PMC2225435/ /pubmed/18254653 http://dx.doi.org/10.1371/journal.pmed.0050028 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article García-Lerma, J. Gerardo Otten, Ron A Qari, Shoukat H Jackson, Eddie Cong, Mian-er Masciotra, Silvina Luo, Wei Kim, Caryn Adams, Debra R Monsour, Michael Lipscomb, Jonathan Johnson, Jeffrey A Delinsky, David Schinazi, Raymond F Janssen, Robert Folks, Thomas M Heneine, Walid Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title | Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title_full | Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title_fullStr | Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title_full_unstemmed | Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title_short | Prevention of Rectal SHIV Transmission in Macaques by Daily or Intermittent Prophylaxis with Emtricitabine and Tenofovir |
title_sort | prevention of rectal shiv transmission in macaques by daily or intermittent prophylaxis with emtricitabine and tenofovir |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2225435/ https://www.ncbi.nlm.nih.gov/pubmed/18254653 http://dx.doi.org/10.1371/journal.pmed.0050028 |
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