Dynamics of HIV DNA reservoir seeding in a cohort of superinfected Kenyan women.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
02 2020
Historique:
received: 27 08 2019
accepted: 16 12 2019
revised: 18 02 2020
pubmed: 6 2 2020
medline: 6 5 2020
entrez: 6 2 2020
Statut: epublish

Résumé

A reservoir of HIV-infected cells that persists despite suppressive antiretroviral therapy (ART) is the source of viral rebound upon ART cessation and the major barrier to a cure. Understanding reservoir seeding dynamics will help identify the best timing for HIV cure strategies. Here we characterize reservoir seeding using longitudinal samples from before and after ART initiation in individuals who sequentially became infected with genetically distinct HIV variants (superinfected). We previously identified cases of superinfection in a cohort of Kenyan women, and the dates of both initial infection and superinfection were determined. Six women, superinfected 0.2-5.2 years after initial infection, were subsequently treated with ART 5.4-18.0 years after initial infection. We performed next-generation sequencing of HIV gag and env RNA from plasma collected during acute infection as well as every ~2 years thereafter until ART initiation, and of HIV DNA from PBMCs collected 0.9-4.8 years after viral suppression on ART. We assessed phylogenetic relationships between HIV DNA reservoir sequences and longitudinal plasma RNA sequences prior to ART, to determine proportions of initial and superinfecting variants in the reservoir. The proportions of initial and superinfection lineage variants present in the HIV DNA reservoir were most similar to the proportions present in HIV RNA immediately prior to ART initiation. Phylogenetic analysis confirmed that the majority of HIV DNA reservoir sequences had the smallest pairwise distance to RNA sequences from timepoints closest to ART initiation. Our data suggest that while reservoir cells are created throughout pre-ART infection, the majority of HIV-infected cells that persist during ART entered the reservoir near the time of ART initiation. We estimate the half-life of pre-ART DNA reservoir sequences to be ~25 months, which is shorter than estimated reservoir decay rates during suppressive ART, implying continual decay and reseeding of the reservoir up to the point of ART initiation.

Identifiants

pubmed: 32023326
doi: 10.1371/journal.ppat.1008286
pii: PPATHOGENS-D-19-01577
pmc: PMC7028291
doi:

Substances chimiques

DNA, Viral 0
env Gene Products, Human Immunodeficiency Virus 0
gag Gene Products, Human Immunodeficiency Virus 0

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1008286

Subventions

Organisme : NIAID NIH HHS
ID : K25 AI155224
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM113246
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI038518
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI126623
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD094718
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015704
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Mark D Pankau (MD)

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Department of Global Health, University of Washington, Seattle, WA, United States of America.

Daniel B Reeves (DB)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.

Elias Harkins (E)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.

Keshet Ronen (K)

Department of Global Health, University of Washington, Seattle, WA, United States of America.

Walter Jaoko (W)

Department of Medical Microbiology, University of Nairobi, Kenyatta National Hospital, Nairobi, Kenya.

Kishor Mandaliya (K)

Coast Provincial General Hospital, Women's Health Project, Mombasa, Kenya.

Susan M Graham (SM)

Department of Global Health, University of Washington, Seattle, WA, United States of America.
Department of Medicine, University of Washington, Seattle, WA, United States of America.
Department of Epidemiology, University of Washington, Seattle, WA, United States of America.

R Scott McClelland (RS)

Department of Global Health, University of Washington, Seattle, WA, United States of America.
Department of Medical Microbiology, University of Nairobi, Kenyatta National Hospital, Nairobi, Kenya.
Department of Medicine, University of Washington, Seattle, WA, United States of America.
Department of Epidemiology, University of Washington, Seattle, WA, United States of America.

Frederick A Matsen Iv (FA)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.

Joshua T Schiffer (JT)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Department of Medicine, University of Washington, Seattle, WA, United States of America.

Julie Overbaugh (J)

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.

Dara A Lehman (DA)

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Department of Global Health, University of Washington, Seattle, WA, United States of America.

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Classifications MeSH