Abstract
HIV causes a chronic infection characterized by depletion of CD4(+) T lymphocytes and the development of opportunistic infections. Despite drugs that inhibit viral spread, HIV infection has been difficult to cure because of uncharacterized reservoirs of infected cells that are resistant to highly active antiretroviral therapy (HAART) and the immune response. Here we used CD34(+) cells from infected people as well as in vitro studies of wild-type HIV to show infection and killing of CD34(+) multipotent hematopoietic progenitor cells (HPCs). In some HPCs, we detected latent infection that stably persisted in cell culture until viral gene expression was activated by differentiation factors. A unique reporter HIV that directly detects latently infected cells in vitro confirmed the presence of distinct populations of active and latently infected HPCs. These findings have major implications for understanding HIV bone marrow pathology and the mechanisms by which HIV causes persistent infection.
MeSH Terms
AC133 Antigen
Antigens, CD/immunology
Antigens, CD34/immunology
CD4-Positive T-Lymphocytes/immunology,virology
Cell Death
Cell Line
Glycoproteins/immunology
HIV Infections/immunology,virology
HIV-1/genetics,physiology
Hematopoietic Stem Cells/virology
Humans
Multipotent Stem Cells/virology
Peptides/immunology
Polymerase Chain Reaction
Virus Activation/physiology
Virus Latency/physiology
Chemicals
AC133 Antigen
Antigens, CD
Antigens, CD34
Glycoproteins
Peptides
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Carter Christoph C
Graduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan, USA.
Onafuwa-Nuga Adewunmi
McNamara Lucy A
Riddell James
Bixby Dale
Savona Michael R
Collins Kathleen L
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