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HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men

Young men who have sex with men (YMSM) are disproportionately affected by HIV and bacterial sexually transmitted infections (STI) including gonorrhea, chlamydia, and syphilis; yet research into the immunologic effects of these infections is typically pursued in siloes. Here, we employed a syndemic a...

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Autores principales: Van Doren, Vanessa E., Smith, S. Abigail, Hu, Yi-Juan, Tharp, Gregory, Bosinger, Steven, Ackerley, Cassie G., Murray, Phillip M., Amara, Rama R., Amancha, Praveen K., Arthur, Robert A., Johnston, H. Richard, Kelley, Colleen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256205/
https://www.ncbi.nlm.nih.gov/pubmed/37253061
http://dx.doi.org/10.1371/journal.ppat.1011219
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author Van Doren, Vanessa E.
Smith, S. Abigail
Hu, Yi-Juan
Tharp, Gregory
Bosinger, Steven
Ackerley, Cassie G.
Murray, Phillip M.
Amara, Rama R.
Amancha, Praveen K.
Arthur, Robert A.
Johnston, H. Richard
Kelley, Colleen F.
author_facet Van Doren, Vanessa E.
Smith, S. Abigail
Hu, Yi-Juan
Tharp, Gregory
Bosinger, Steven
Ackerley, Cassie G.
Murray, Phillip M.
Amara, Rama R.
Amancha, Praveen K.
Arthur, Robert A.
Johnston, H. Richard
Kelley, Colleen F.
author_sort Van Doren, Vanessa E.
collection PubMed
description Young men who have sex with men (YMSM) are disproportionately affected by HIV and bacterial sexually transmitted infections (STI) including gonorrhea, chlamydia, and syphilis; yet research into the immunologic effects of these infections is typically pursued in siloes. Here, we employed a syndemic approach to understand potential interactions of these infections on the rectal mucosal immune environment among YMSM. We enrolled YMSM aged 18–29 years with and without HIV and/or asymptomatic bacterial STI and collected blood, rectal secretions, and rectal tissue biopsies. YMSM with HIV were on suppressive antiretroviral therapy (ART) with preserved blood CD4 cell counts. We defined 7 innate and 19 adaptive immune cell subsets by flow cytometry, the rectal mucosal transcriptome by RNAseq, and the rectal mucosal microbiome by 16S rRNA sequencing and examined the effects of HIV and STI and their interactions. We measured tissue HIV RNA viral loads among YMSM with HIV and HIV replication in rectal explant challenge experiments among YMSM without HIV. HIV, but not asymptomatic STI, was associated with profound alterations in the cellular composition of the rectal mucosa. We did not detect a difference in the microbiome composition associated with HIV, but asymptomatic bacterial STI was associated with a higher probability of presence of potentially pathogenic taxa. When examining the rectal mucosal transcriptome, there was evidence of statistical interaction; asymptomatic bacterial STI was associated with upregulation of numerous inflammatory genes and enrichment for immune response pathways among YMSM with HIV, but not YMSM without HIV. Asymptomatic bacterial STI was not associated with differences in tissue HIV RNA viral loads or in HIV replication in explant challenge experiments. Our results suggest that asymptomatic bacterial STI may contribute to inflammation particularly among YMSM with HIV, and that future research should examine potential harms and interventions to reduce the health impact of these syndemic infections.
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spelling pubmed-102562052023-06-10 HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men Van Doren, Vanessa E. Smith, S. Abigail Hu, Yi-Juan Tharp, Gregory Bosinger, Steven Ackerley, Cassie G. Murray, Phillip M. Amara, Rama R. Amancha, Praveen K. Arthur, Robert A. Johnston, H. Richard Kelley, Colleen F. PLoS Pathog Research Article Young men who have sex with men (YMSM) are disproportionately affected by HIV and bacterial sexually transmitted infections (STI) including gonorrhea, chlamydia, and syphilis; yet research into the immunologic effects of these infections is typically pursued in siloes. Here, we employed a syndemic approach to understand potential interactions of these infections on the rectal mucosal immune environment among YMSM. We enrolled YMSM aged 18–29 years with and without HIV and/or asymptomatic bacterial STI and collected blood, rectal secretions, and rectal tissue biopsies. YMSM with HIV were on suppressive antiretroviral therapy (ART) with preserved blood CD4 cell counts. We defined 7 innate and 19 adaptive immune cell subsets by flow cytometry, the rectal mucosal transcriptome by RNAseq, and the rectal mucosal microbiome by 16S rRNA sequencing and examined the effects of HIV and STI and their interactions. We measured tissue HIV RNA viral loads among YMSM with HIV and HIV replication in rectal explant challenge experiments among YMSM without HIV. HIV, but not asymptomatic STI, was associated with profound alterations in the cellular composition of the rectal mucosa. We did not detect a difference in the microbiome composition associated with HIV, but asymptomatic bacterial STI was associated with a higher probability of presence of potentially pathogenic taxa. When examining the rectal mucosal transcriptome, there was evidence of statistical interaction; asymptomatic bacterial STI was associated with upregulation of numerous inflammatory genes and enrichment for immune response pathways among YMSM with HIV, but not YMSM without HIV. Asymptomatic bacterial STI was not associated with differences in tissue HIV RNA viral loads or in HIV replication in explant challenge experiments. Our results suggest that asymptomatic bacterial STI may contribute to inflammation particularly among YMSM with HIV, and that future research should examine potential harms and interventions to reduce the health impact of these syndemic infections. Public Library of Science 2023-05-30 /pmc/articles/PMC10256205/ /pubmed/37253061 http://dx.doi.org/10.1371/journal.ppat.1011219 Text en © 2023 Van Doren et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Van Doren, Vanessa E.
Smith, S. Abigail
Hu, Yi-Juan
Tharp, Gregory
Bosinger, Steven
Ackerley, Cassie G.
Murray, Phillip M.
Amara, Rama R.
Amancha, Praveen K.
Arthur, Robert A.
Johnston, H. Richard
Kelley, Colleen F.
HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title_full HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title_fullStr HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title_full_unstemmed HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title_short HIV, asymptomatic STI, and the rectal mucosal immune environment among young men who have sex with men
title_sort hiv, asymptomatic sti, and the rectal mucosal immune environment among young men who have sex with men
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256205/
https://www.ncbi.nlm.nih.gov/pubmed/37253061
http://dx.doi.org/10.1371/journal.ppat.1011219
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