Higher HIV-1 Env gp120-Specific Antibody-Dependent Cellular Cytotoxicity (ADCC) Activity Is Associated with Lower Levels of Defective HIV-1 Provirus.

CS-IPDA HIV envelope (Env) HIV provirus HIV reservoir HIV-1 antibody antibody-dependent cellular cytotoxicity (ADCC) defective provirus intact provirus pediatric HIV

Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
06 10 2023
Historique:
received: 11 09 2023
revised: 03 10 2023
accepted: 03 10 2023
medline: 30 10 2023
pubmed: 28 10 2023
entrez: 28 10 2023
Statut: epublish

Résumé

A cure for HIV-1 (HIV) remains unrealized due to a reservoir of latently infected cells that persist during antiretroviral therapy (ART), with reservoir size associated with adverse health outcomes and inversely with time to viral rebound upon ART cessation. Once established during ART, the HIV reservoir decays minimally over time; thus, understanding factors that impact the size of the HIV reservoir near its establishment is key to improving the health of people living with HIV and for the development of novel cure strategies. Yet, to date, few correlates of HIV reservoir size have been identified, particularly in pediatric populations. Here, we employed a cross-subtype intact proviral DNA assay (CS-IPDA) to quantify HIV provirus between one- and two-years post-ART initiation in a cohort of Kenyan children (n = 72), which had a median of 99 intact (range: 0-2469), 1340 defective (range: 172-3.84 × 10

Identifiants

pubmed: 37896832
pii: v15102055
doi: 10.3390/v15102055
pmc: PMC10611199
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00194545']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI076105
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD094718
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015704
Pays : United States

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Auteurs

Ryan Yucha (R)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98195, USA.

Morgan L Litchford (ML)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

Carolyn S Fish (CS)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

Zak A Yaffe (ZA)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA.
Medical Scientist Training Program, University of Washington, Seattle, WA 98195, USA.

Barbra A Richardson (BA)

Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

Elizabeth Maleche-Obimbo (E)

Department of Pediatrics and Child Health, University of Nairobi, Nairobi P.O. Box 30197, Kenya.

Grace John-Stewart (G)

Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Department of Medicine, University of Washington, Seattle, WA 98195, USA.
Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Department of Epidemiology, University of Washington, Seattle, WA 98195, USA.

Dalton Wamalwa (D)

Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Department of Pediatrics and Child Health, University of Nairobi, Nairobi P.O. Box 30197, Kenya.

Julie Overbaugh (J)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.

Dara A Lehman (DA)

Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA.
Department of Global Health, University of Washington, Seattle, WA 98195, USA.

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