Aug 2026· Frontiers in Immunology· Vol 17· 0 citations· 46 references
Medicine
TL;DR
The study reveals a distinct proviral landscape in ART-treated INRs, characterized by elevated levels of intact proviral genomes, and suggests that the intact component of the reservoir may represent a clinically relevant feature of incomplete immune reconstitution.
Abstract
Background Immunological non-responders (INRs) and immunological responders (IRs) exhibit distinct patterns of immune reconstitution despite suppressive antiretroviral therapy (ART); however, the genetic characteristics of the HIV-1 reservoir in these groups remain poorly understood. This study investigates the landscape of HIV-1 proviruses in INRs and IRs, and its potential association with immune reconstitution. Methods Peripheral blood mononuclear cells (PBMCs) from 10 ART-treated INRs and 10 IRs were analyzed using near-full-length HIV-1 DNA amplification and PacBio third-generation sequencing to characterize genetically intact and defective proviral genomes. Intact open reading frames (ORFs) were further inferred using the CFEIntact tool. Results Compared with IRs, INRs had a higher total proviral genome per 106 PBMCs, although the difference did not reach statistically significance. INRs also displayed a significantly higher level of intact proviral genomes per 106 PBMCs and a trend toward a higher proportion of intact sequences. Defective proviruses remained the predominant component of the reservoir in both groups and were broadly comparable in number and composition. In both cohorts, proviral defects were more frequently observed in the 3′ half of the genome. Discussion Our study reveals a distinct proviral landscape in ART-treated INRs, characterized by elevated levels of intact proviral genomes. These observations suggest that the intact component of the reservoir may represent a clinically relevant feature of incomplete immune reconstitution, and provide a rationale for further studies of reservoir-directed interventions in this population.
Abstract: Antiretroviral therapy has rendered HIV a manageable chronic infection, but integrated
proviral DNA within long-lived CD4+ memory T cells persists indefinitely and constitutes both a
barrier to cure and an archive of the patient’s virologic history. Genotypic resistance testing
performed on proviral DNA from...
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Defective HIV proviruses make up the majority of the proviral reservoir across blood and tissue compartments and may contribute to chronic inflammation, antigen persistence, and neuropathology in ART-suppressed PWH.
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BACKGROUND
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