HIV-1 control in vivo is related to the number but not the fraction of infected cells with viral unspliced RNA

Author:

Capoferri Adam A.12ORCID,Wiegand Ann1,Hong Feiyu3,Jacobs Jana L.3,Spindler Jonathan1,Musick Andrew4,Bale Michael J.15,Shao Wei4,Sobolewski Michele D.3,Cillo Anthony R.6,Luke Brian T.4,Fennessey Christine M.7,Gorelick Robert J.7,Hoh Rebecca8,Halvas Elias K.3,Deeks Steven G.8,Coffin John M.9,Mellors John W.3,Kearney Mary F.1

Affiliation:

1. HIV Dynamics and Replication Program, National Cancer Institute, Frederick, MD 21702

2. Department of Microbiology and Immunology, Georgetown University, Washington, DC 20007

3. Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213

4. Leidos Biomedical Research, Inc., Frederick National Laboratories for Cancer Research, Frederick, MD 21702

5. Laboratory of Epigenetics and Immunity, Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10065

6. Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261

7. AIDS and Cancer Virus Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702

8. Department of Medicine, University of California, San Francisco, CA 94143

9. Department of Molecular Biology and Microbiology, Tufts University, Boston, MA 02111

Abstract

In the absence of antiretroviral therapy (ART), a subset of individuals, termed HIV controllers, have levels of plasma viremia that are orders of magnitude lower than non-controllers (NC) who are at higher risk for HIV disease progression. In addition to having fewer infected cells resulting in fewer cells with HIV RNA, it is possible that lower levels of plasma viremia in controllers are due to a lower fraction of the infected cells having HIV-1 unspliced RNA (HIV usRNA) compared with NC. To directly test this possibility, we used sensitive and quantitative single-cell sequencing methods to compare the fraction of infected cells that contain one or more copies of HIV usRNA in peripheral blood mononuclear cells (PBMC) obtained from controllers and NC. The fraction of infected cells containing HIV usRNA did not differ between the two groups. Rather, the levels of viremia were strongly associated with the total number of infected cells that had HIV usRNA, as reported by others, with controllers having 34-fold fewer infected cells per million PBMC. These results reveal that viremic control is not associated with a lower fraction of proviruses expressing HIV usRNA, unlike what is reported for elite controllers, but is only related to having fewer infected cells overall, maybe reflecting greater immune clearance of infected cells. Our findings show that proviral silencing is not a key mechanism for viremic control and will help to refine strategies toward achieving HIV remission without ART.

Funder

NCI

National Cancer Institute

Leidos Biomedical

NIH

HHS | NIH | NIAID | Division of Intramural Research

Publisher

Proceedings of the National Academy of Sciences

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