Dating reservoir formation in virologically suppressed people living with HIV-1 in Rakai, Uganda

Author:

Kankaka Edward Nelson12ORCID,Redd Andrew D234,Khan Amjad5,Reynolds Steven J123,Saraf Sharada3,Kirby Charles2,Lynch Briana3,Hackman Jada3ORCID,Tomusange Stephen1,Kityamuweesi Taddeo1,Jamiru Samiri1,Anok Aggrey1,Buule Paul1,Bruno Daniel6,Martens Craig6,Chang Larry W2,Quinn Thomas C23,Prodger Jessica L7,Poon Art5ORCID

Affiliation:

1. Research Department, Rakai Health Sciences Program , 4-6 Sanitary Lane, Old Bukoba Road, Kalisizo 256, Uganda

2. Division of Infectious Diseases, Johns Hopkins University School of Medicine , 615 N. Wolfe Street, Baltimore, MD 21211, USA

3. Laboratory of Immunoregulation, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , 5601 Fishers Lane, MSC, Bethesda, MD 9806, USA

4. Institute of Infectious Disease and Molecular Medicine, University of Cape Town , Faculty of Health Sciences, Anzio Rd, Observatory, Cape Town 7925, South Africa

5. Department of Pathology, Schulich School of Medicine and Dentistry, Western University , 1151 Richmond Street, London, Ontario N6A 5K8, Canada

6. Genomic Unit, Rocky Mountain Laboratories, NIAID, NIH , 904 South Fourth Street, Hamilton, MT 59840, USA

7. Department of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western University , 1151 Richmond Street, London, Ontario N6A 5K8, Canada

Abstract

Abstract The timing of the establishment of the HIV latent viral reservoir (LVR) is of particular interest, as there is evidence that proviruses are preferentially archived at the time of antiretroviral therapy (ART) initiation. Quantitative viral outgrowth assays (QVOAs) were performed using Peripheral Blood Mononuclear Cells (PBMC) collected from Ugandans living with HIV who were virally suppressed on ART for >1 year, had known seroconversion windows, and at least two archived ART-naïve plasma samples. QVOA outgrowth populations and pre-ART plasma samples were deep sequenced for the pol and gp41 genes. The bayroot program was used to estimate the date that each outgrowth virus was incorporated into the reservoir. Bayroot was also applied to previously published data from a South African cohort. In the Ugandan cohort (n = 11), 87.9 per cent pre-ART and 56.3 per cent viral outgrowth sequences were unique. Integration dates were estimated to be relatively evenly distributed throughout viremia in 9/11 participants. In contrast, sequences from the South African cohort (n = 9) were more commonly estimated to have entered the LVR close to ART initiation, as previously reported. Timing of LVR establishment is variable between populations and potentially viral subtypes, which could limit the effectiveness of interventions that target the LVR only at ART initiation.

Funder

Gilead Sciences

amfAR, The Foundation for AIDS Research

Canada Research Chairs

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

Fogarty International Center

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

Reference34 articles.

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3. Immediate Antiviral Therapy Appears to Restrict Resting CD4+ Cell HIV-1 Infection without Accelerating the Decay of Latent Infection;Archin;Proceedings of the National Academy of Sciences of the United States of America,2012

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5. HIV-1 Variants are Archived Throughout Infection and Persist in the Reservoir;Brooks;PLOS Pathogens,2020

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