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Single-cell characterization of the gastrointestinal HIV reservoir reveals heterogeneous cellular phenotypes
Jackson J. Peterson, Shipra Chandel, Katherine James, Elizabeth S. Bennett, Vincent Wu, Cory H. White, Brigitte Allard, Matthew Clohosey, Taylor Whitaker, Caroline Baker, Susan Pedersen, Anne F. Peery, Cynthia L. Gay, Michael R. Betts, David M. Margolis, Nancie M. Archin, Edward P. Browne
Jackson J. Peterson, Shipra Chandel, Katherine James, Elizabeth S. Bennett, Vincent Wu, Cory H. White, Brigitte Allard, Matthew Clohosey, Taylor Whitaker, Caroline Baker, Susan Pedersen, Anne F. Peery, Cynthia L. Gay, Michael R. Betts, David M. Margolis, Nancie M. Archin, Edward P. Browne
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Research Article AIDS/HIV Immunology

Single-cell characterization of the gastrointestinal HIV reservoir reveals heterogeneous cellular phenotypes

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Abstract

Human gastrointestinal (GI) tissues are a major site of HIV-1 viral persistence, but the nature of the GI reservoir remains poorly described. To characterize the GI HIV reservoir, we profiled cells from GI tissue and matched PBMCs from 10 people with HIV on antiretroviral therapy using single-cell RNA sequencing. We identified distinct compartment-specific patterns of gene expression, highlighting key differences between blood and colon CD4+ T cell populations. vRNA+ cells from both blood and GI tissue were heterogeneous and found in multiple subtypes of CD4+ T cells, although vRNA+ cells were particularly enriched in cells with Th17 or Treg17 phenotypes. Transcriptomic comparison of HIV vRNA+ and vRNA– T cells revealed 116 differentially expressed genes that were associated with HIV infection, including ZBED2, MAF, and IL17F. These data provide what we believe to be new information regarding the GI-resident HIV reservoir and suggest that compartment-specific patterns of gene expression are associated with HIV infection.

Authors

Jackson J. Peterson, Shipra Chandel, Katherine James, Elizabeth S. Bennett, Vincent Wu, Cory H. White, Brigitte Allard, Matthew Clohosey, Taylor Whitaker, Caroline Baker, Susan Pedersen, Anne F. Peery, Cynthia L. Gay, Michael R. Betts, David M. Margolis, Nancie M. Archin, Edward P. Browne

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Figure 1

Single-cell proteomic and transcriptomic profiling of colon and blood cells from people with HIV.

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Single-cell proteomic and transcriptomic profiling of colon and blood ce...
(A) Schematic overview of experimental design and sample processing pipeline. (B) Uniform manifold approximation and projection (UMAP) visualization of the combined dataset of scRNAseq and surface protein abundance for matched colon and blood cells from 10 people with HIV (PWH) on antiretroviral therapy (ART) and 1 HIV-seronegative participant. Visualization shown is after reciprocal principal component analysis (RPCA) correction. Top: Blood-derived cells highlighted in red. Bottom: Colon-derived cells highlighted in blue. (C) UMAP visualization of cell clusters colored and labeled by annotated cell type. (D) Dot plot of gene expression levels from scRNAseq dataset, including both stimulated and unstimulated cells, organized by clusters (y axis) and gene of interest (x axis). Shown are key markers used in identification and annotation of cell types.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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