Lymphoid B cells upregulate HIV-1 ex vivo and are linked to its expression in vivo

B cell follicles in secondary lymphoid tissues are major sites of HIV expression in untreated people living with HIV (PLWH), but whether lymphoid B cells promote HIV expression in CD4+ T cells is unknown. Using a tonsil model and flow cytometry, germinal center B cells induced HIV expression in follicular helper CD4+ T cells (TFH) in a concentration-, contact-, and major histocompatibility complex class II (MHC-II)-dependent manner. Non-naïve tonsil B cells also induced HIV expression in nonTFH CD4+ T cells that was MHC-II restricted. In situ hybridization and immunofluorescent staining of lymph node sections from six PLWH on long-term antiretroviral therapy (ART) and six ART-naïve PLWH demonstrated most HIV RNA-expressing (vRNA+) cells were adjacent to at least one B cell. In both groups, vRNA+ cells per mm2 were elevated in B cell follicles, particularly after adjusting for CD3+CD4+ frequencies. TFH (PD-1+BCL6+) were a minority of vRNA+ cells in all PLWH. In contrast to ART-naïve PLWH, most vRNA+ cells in PLWH on ART resided outside follicles, and were preferentially adjacent to extrafollicular B cells. Thus, B cells upregulate HIV expression largely through cognate interactions in vitro and are linked to HIV expression in secondary lymphoid tissues.

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Publication Details

Journal
PLoS Pathogens
Published
2025-12-01
DOI
https://doi.org/10.1371/journal.ppat.1013661
Primary Topic
HIV Research and Treatment
Type
article
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article

Lymphoid B cells upregulate HIV-1 ex vivo and are linked to its expression in vivo

David Parry, Martin D. McCarter, Joy M. Folkvord, Amie L. Meditz et al.
PLoS Pathogens
HIV Research and Treatment
article

Lymphoid B cells upregulate HIV-1 ex vivo and are linked to its expression in vivo

David Parry, Martin D. McCarter, Joy M. Folkvord, Amie L. Meditz, Matthew T. Ollerton, Elizabeth Connick, Cecilia M. Shikuma, Fred J. Yost, Veronica Bush
article en

Abstract

B cell follicles in secondary lymphoid tissues are major sites of HIV expression in untreated people living with HIV (PLWH), but whether lymphoid B cells promote HIV expression in CD4+ T cells is unknown. Using a tonsil model and flow cytometry, germinal center B cells induced HIV expression in follicular helper CD4+ T cells (TFH) in a concentration-, contact-, and major histocompatibility complex class II (MHC-II)-dependent manner. Non-naïve tonsil B cells also induced HIV expression in nonTFH CD4+ T cells that was MHC-II restricted. In situ hybridization and immunofluorescent staining of lymph node sections from six PLWH on long-term antiretroviral therapy (ART) and six ART-naïve PLWH demonstrated most HIV RNA-expressing (vRNA+) cells were adjacent to at least one B cell. In both groups, vRNA+ cells per mm2 were elevated in B cell follicles, particularly after adjusting for CD3+CD4+ frequencies. TFH (PD-1+BCL6+) were a minority of vRNA+ cells in all PLWH. In contrast to ART-naïve PLWH, most vRNA+ cells in PLWH on ART resided outside follicles, and were preferentially adjacent to extrafollicular B cells. Thus, B cells upregulate HIV expression largely through cognate interactions in vitro and are linked to HIV expression in secondary lymphoid tissues.

PLoS PathogensVol. 21(12)
University of Hawaiʻi at Mānoa (US), University of Arizona (US), Banner - University Medical Center Tucson (US), National Center for Infectious Diseases (US), University of Colorado Anschutz Medical Campus (US)
Openalex Percentile: Top 60%
HIV Research and Treatment
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