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The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention

Most HIV transmissions among men who have sex with men (MSM), the group that accounted for 67% of new US infections in 2014, occur via exposure to the rectal mucosa. However, it is unclear how the act of condomless receptive anal intercourse (CRAI) may alter the mucosal immune environment in HIV neg...

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Autores principales: Kelley, Colleen F., Kraft, Colleen S., de Man, Tom J.B., Duphare, Chandni, Lee, Hyun-Woo, Yang, Jing, Easley, Kirk A., Tharp, Gregory K., Mulligan, Mark J., Sullivan, Patrick S., Bosinger, Steven E., Amara, Rama R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433931/
https://www.ncbi.nlm.nih.gov/pubmed/27848950
http://dx.doi.org/10.1038/mi.2016.97
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author Kelley, Colleen F.
Kraft, Colleen S.
de Man, Tom J.B.
Duphare, Chandni
Lee, Hyun-Woo
Yang, Jing
Easley, Kirk A.
Tharp, Gregory K.
Mulligan, Mark J.
Sullivan, Patrick S.
Bosinger, Steven E.
Amara, Rama R.
author_facet Kelley, Colleen F.
Kraft, Colleen S.
de Man, Tom J.B.
Duphare, Chandni
Lee, Hyun-Woo
Yang, Jing
Easley, Kirk A.
Tharp, Gregory K.
Mulligan, Mark J.
Sullivan, Patrick S.
Bosinger, Steven E.
Amara, Rama R.
author_sort Kelley, Colleen F.
collection PubMed
description Most HIV transmissions among men who have sex with men (MSM), the group that accounted for 67% of new US infections in 2014, occur via exposure to the rectal mucosa. However, it is unclear how the act of condomless receptive anal intercourse (CRAI) may alter the mucosal immune environment in HIV negative MSM. Here, we performed a comprehensive characterization of the rectal mucosal immune environment for the phenotype and production of pro-inflammatory cytokines by CD4 and CD8 T cells, global transcriptomic analyses, and the composition of microbiota in HIV negative MSM. Our results show that compared to men who had never engaged in anal intercourse, the rectal mucosa of MSM engaging in CRAI has a distinct phenotype characterized by higher levels of Th17 cells, greater CD8+ T cell proliferation and production of pro-inflammatory cytokines, molecular signatures associated with mucosal injury and repair likely mediated by innate immune cells, and a microbiota enriched for the Prevotellaceae family. These data provide a high-resolution model of the immunological, molecular, and microbiological perturbations induced by CRAI, will have direct utility in understanding rectal HIV transmission among MSM, and will enhance the design of future biomedical prevention interventions, including candidate HIV vaccines.
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spelling pubmed-54339312017-06-19 The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention Kelley, Colleen F. Kraft, Colleen S. de Man, Tom J.B. Duphare, Chandni Lee, Hyun-Woo Yang, Jing Easley, Kirk A. Tharp, Gregory K. Mulligan, Mark J. Sullivan, Patrick S. Bosinger, Steven E. Amara, Rama R. Mucosal Immunol Article Most HIV transmissions among men who have sex with men (MSM), the group that accounted for 67% of new US infections in 2014, occur via exposure to the rectal mucosa. However, it is unclear how the act of condomless receptive anal intercourse (CRAI) may alter the mucosal immune environment in HIV negative MSM. Here, we performed a comprehensive characterization of the rectal mucosal immune environment for the phenotype and production of pro-inflammatory cytokines by CD4 and CD8 T cells, global transcriptomic analyses, and the composition of microbiota in HIV negative MSM. Our results show that compared to men who had never engaged in anal intercourse, the rectal mucosa of MSM engaging in CRAI has a distinct phenotype characterized by higher levels of Th17 cells, greater CD8+ T cell proliferation and production of pro-inflammatory cytokines, molecular signatures associated with mucosal injury and repair likely mediated by innate immune cells, and a microbiota enriched for the Prevotellaceae family. These data provide a high-resolution model of the immunological, molecular, and microbiological perturbations induced by CRAI, will have direct utility in understanding rectal HIV transmission among MSM, and will enhance the design of future biomedical prevention interventions, including candidate HIV vaccines. 2016-11-16 2017-07 /pmc/articles/PMC5433931/ /pubmed/27848950 http://dx.doi.org/10.1038/mi.2016.97 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kelley, Colleen F.
Kraft, Colleen S.
de Man, Tom J.B.
Duphare, Chandni
Lee, Hyun-Woo
Yang, Jing
Easley, Kirk A.
Tharp, Gregory K.
Mulligan, Mark J.
Sullivan, Patrick S.
Bosinger, Steven E.
Amara, Rama R.
The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title_full The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title_fullStr The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title_full_unstemmed The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title_short The Rectal Mucosa and Condomless Receptive Anal Intercourse in HIV Negative MSM: Implications for HIV Transmission and Prevention
title_sort rectal mucosa and condomless receptive anal intercourse in hiv negative msm: implications for hiv transmission and prevention
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433931/
https://www.ncbi.nlm.nih.gov/pubmed/27848950
http://dx.doi.org/10.1038/mi.2016.97
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