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JCI Insight. 2019 Jun 20;4(12). pii: 128432. doi: 10.1172/jci.insight.128432. eCollection 2019 Jun 20.

Clones of infected cells arise early in HIV-infected individuals.

Author information

1
Department of Molecular Biology and Microbiology, Tufts University, Boston, Massachusetts, USA.
2
Cancer Research Technology Program, and.
3
Department of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
4
Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
5
Advanced Biomedical Computational Science, Frederick National Laboratory for Cancer Research, Frederick Maryland, USA.
6
HIV Dynamics and Replication Program, NCI-Frederick, Frederick, Maryland, USA.

Abstract

In HIV-infected individuals on long-term antiretroviral therapy (ART), more than 40% of the infected cells are in clones. Although most HIV proviruses present in individuals on long-term ART are defective, including those in clonally expanded cells, there is increasing evidence that clones carrying replication-competent proviruses are common in patients on long-term ART and form part of the HIV reservoir that makes it impossible to cure HIV infection with current ART alone. Given the importance of clonal expansion in HIV persistence, we determined how soon after HIV acquisition infected clones can grow large enough to be detected (clones larger than ca. 1 × 105 cells). We studied 12 individuals sampled in early HIV infection (Fiebig stage III-V/VI) and 5 who were chronically infected. The recently infected individuals were started on ART at or near the time of diagnosis. We isolated more than 6,500 independent integration sites from peripheral blood mononuclear cells before ART was initiated and after 0.5-18 years of suppressive ART. Some infected clones could be detected approximately 4 weeks after HIV infection and some of these clones persisted for years. The results help to explain how the reservoir is established early and persists for years.

KEYWORDS:

AIDS/HIV; Clonal selection; T cells

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