HIVconsv Vaccines and Romidepsin in Early-Treated HIV-1-Infected Individuals: Safety, Immunogenicity and Effect on the Viral Reservoir (Study BCN02).
AIDS Vaccines
/ immunology
Adult
Antiviral Agents
/ therapeutic use
Depsipeptides
/ therapeutic use
Disease Reservoirs
Drug Therapy, Combination
Female
HIV Infections
/ drug therapy
HIV-1
/ physiology
Histone Deacetylase Inhibitors
/ therapeutic use
Humans
Male
Middle Aged
Pilot Projects
Viral Load
Viremia
Virus Latency
HDAC inhibitor
HIVconsv
early-treatment
kick&kill strategy
romidepsin
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2020
2020
Historique:
received:
13
02
2020
accepted:
09
04
2020
entrez:
22
5
2020
pubmed:
22
5
2020
medline:
18
3
2021
Statut:
epublish
Résumé
Kick&kill strategies combining drugs aiming to reactivate the viral reservoir with therapeutic vaccines to induce effective cytotoxic immune responses hold potential to achieve a functional cure for HIV-1 infection. Here, we report on an open-label, single-arm, phase I clinical trial, enrolling 15 early-treated HIV-1-infected individuals, testing the combination of the histone deacetylase inhibitor romidepsin as a latency-reversing agent and the MVA.HIVconsv vaccine. Romidepsin treatment resulted in increased histone acetylation, cell-associated HIV-1 RNA, and T-cell activation, which were associated with a marginally significant reduction of the viral reservoir. Vaccinations boosted robust and broad HIVconsv-specific T cells, which were strongly refocused toward conserved regions of the HIV-1 proteome. During a monitored ART interruption phase using plasma viral load over 2,000 copies/ml as a criterium for ART resumption, 23% of individuals showed sustained suppression of viremia up to 32 weeks without evidence for reseeding the viral reservoir. Results from this pilot study show that the combined kick&kill intervention was safe and suggest a role for this strategy in achieving an immune-driven durable viremic control.
Identifiants
pubmed: 32435247
doi: 10.3389/fimmu.2020.00823
pmc: PMC7218169
doi:
Substances chimiques
AIDS Vaccines
0
Antiviral Agents
0
Depsipeptides
0
Histone Deacetylase Inhibitors
0
romidepsin
CX3T89XQBK
Types de publication
Clinical Trial, Phase I
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
823Subventions
Organisme : Medical Research Council
ID : G1001757
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N023668/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : P01 AI131568
Pays : United States
Organisme : Medical Research Council
ID : G0701669
Pays : United Kingdom
Informations de copyright
Copyright © 2020 Mothe, Rosás-Umbert, Coll, Manzardo, Puertas, Morón-López, Llano, Miranda, Cedeño, López, Alarcón-Soto, Melis, Langohr, Barriocanal, Toro, Ruiz, Rovira, Carrillo, Meulbroek, Crook, Wee, Miró, Clotet, Valle, Martinez-Picado, Hanke, Brander, Moltó and the BCN02 Study Investigators.
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