Distinct phases of immune system programming during ART-suppressed immunodeficiency virus infection

People living with HIV (PLWH) on suppressive antiretroviral therapy (ART) can face non-AIDS complications, partially driven by chronic immune activation. To define immune perturbations during ART-suppressed viral infection, we performed longitudinal single-cell transcriptomic and plasma proteomic analyses of rhesus macaques infected with SIVmac239M and treated with ART for 70 weeks. We identified broad, bi-phasic immune changes. Acute infection involves an interferon-driven signature, correlated with viral replication, which largely resolves with viral control. Cell-associated virus correlated with interferon-stimulated genes in most tissues; however, this was blunted in gut-associated lymph nodes, a feature that may contribute to reservoir persistence. Separate alterations manifest 54–66 weeks post-infection, after 40 weeks of viral suppression, including broad TGF-β and NF-κB signaling and discrete bursts of inflammatory monocytes, largely restricted to bone marrow. These data highlight the bi-phasic remodeling of long-term ART-suppressed HIV, identifying specific tissues and cell populations with dysregulation, with implications for the treatment of PLWH.

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Publication Details

Journal
Cell Reports
Published
2026-09-30
DOI
https://doi.org/10.1016/j.celrep.2026.118035
Primary Topic
HIV Research and Treatment
Type
article
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article

Distinct phases of immune system programming during ART-suppressed immunodeficiency virus infection

Jacob D. Estes, Sebastián Benjamín, Karina Belica, Afam A. Okoye et al.
Cell Reports
HIV Research and Treatment
article

Distinct phases of immune system programming during ART-suppressed immunodeficiency virus infection

Jacob D. Estes, Sebastián Benjamín, Karina Belica, Afam A. Okoye, Jeffrey D. Lifson, Morgan Chaunzwa, Brandon F. Keele, Scott G. Hansen, Andrea N. Selseth, Benjamin N. Bimber, Gregory J. Boggy, Louis J. Picker, Sohita Ojha, Shana Feltham, Maanasa Kaza, Michael Nekorchuk, Benjamin Varco-Merth, G.W. McElfresh, Kathleen Busman-Sahay, Dan H. Barouch
article en

Abstract

People living with HIV (PLWH) on suppressive antiretroviral therapy (ART) can face non-AIDS complications, partially driven by chronic immune activation. To define immune perturbations during ART-suppressed viral infection, we performed longitudinal single-cell transcriptomic and plasma proteomic analyses of rhesus macaques infected with SIVmac239M and treated with ART for 70 weeks. We identified broad, bi-phasic immune changes. Acute infection involves an interferon-driven signature, correlated with viral replication, which largely resolves with viral control. Cell-associated virus correlated with interferon-stimulated genes in most tissues; however, this was blunted in gut-associated lymph nodes, a feature that may contribute to reservoir persistence. Separate alterations manifest 54–66 weeks post-infection, after 40 weeks of viral suppression, including broad TGF-β and NF-κB signaling and discrete bursts of inflammatory monocytes, largely restricted to bone marrow. These data highlight the bi-phasic remodeling of long-term ART-suppressed HIV, identifying specific tissues and cell populations with dysregulation, with implications for the treatment of PLWH.

Cell ReportsVol. 45(10)
Oregon National Primate Research Center (US), Beth Israel Deaconess Medical Center (US), Oregon Health & Science University (US), Ragon Institute of MGH, MIT and Harvard (US), Frederick National Laboratory for Cancer Research (US), Vaccine and Gene Therapy Institute
Good health and well-being
Openalex Percentile: Top 13%
HIV Research and Treatment
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