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Antiretroviral therapy alone versus antiretroviral therapy with a kick and kill approach, on measures of the HIV reservoir in participants with recent HIV infection (the RIVER trial): a phase 2, randomised trial.
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- Author(s): Fidler, Sarah1,2 (AUTHOR) ; Stöhr, Wolfgang3 (AUTHOR); Pace, Matt4,5 (AUTHOR); Dorrell, Lucy4,6 (AUTHOR); Lever, Andrew7,8 (AUTHOR); Pett, Sarah3,9,10 (AUTHOR); Kinloch-de Loes, Sabine11,12 (AUTHOR); Fox, Julie13,14 (AUTHOR); Clarke, Amanda15,16,17 (AUTHOR); Nelson, Mark18 (AUTHOR); Thornhill, John1,2 (AUTHOR); Khan, Maryam1,2 (AUTHOR); Fun, Axel19 (AUTHOR); Bandara, Mikaila20 (AUTHOR); Kelly, Damian21 (AUTHOR); Kopycinski, Jakub4,6 (AUTHOR); Hanke, Tomáš4,22 (AUTHOR); Yang, Hongbing4,6 (AUTHOR); Bennett, Rachel3 (AUTHOR); Johnson, Margaret23 (AUTHOR)
- Source:
Lancet. 3/14/2020, Vol. 395 Issue 10227, p888-898. 11p.- Subject Terms:
*HIV infections; *ANTIRETROVIRAL agents; *HISTONE deacetylase inhibitors; *HIV; *RESERVOIRS; *DNA analysis; *RESEARCH; *RESEARCH methodology; *AIDS vaccines; *PUBLIC health; *RNA; *EVALUATION research; *MEDICAL cooperation; *TREATMENT effectiveness; *COMPARATIVE studies; *RESEARCH funding; *ENZYME inhibitors - Source:
- Additional Information
- Subject Terms:
- Subject Terms:
- Abstract:
Background: Antiretroviral therapy (ART) cannot cure HIV infection because of a persistent reservoir of latently infected cells. Approaches that force HIV transcription from these cells, making them susceptible to killing-termed kick and kill regimens-have been explored as a strategy towards an HIV cure. RIVER is the first randomised trial to determine the effect of ART-only versus ART plus kick and kill on markers of the HIV reservoir.Methods: This phase 2, open-label, multicentre, randomised, controlled trial was undertaken at six clinical sites in the UK. Patients aged 18-60 years who were confirmed as HIV-positive within a maximum of the past 6 months and started ART within 1 month from confirmed diagnosis were randomly assigned by a computer generated randomisation list to receive ART-only (control) or ART plus the histone deacetylase inhibitor vorinostat (the kick) and replication-deficient viral vector T-cell inducing vaccines encoding conserved HIV sequences ChAdV63. HIVconsv-prime and MVA.HIVconsv-boost (the kill; ART + V + V; intervention). The primary endpoint was total HIV DNA isolated from peripheral blood CD4+ T-cells at weeks 16 and 18 after randomisation. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, NCT02336074.Findings: Between June 14, 2015 and Jul 11, 2017, 60 men with HIV were randomly assigned to receive either an ART-only (n=30) or an ART + V + V (n=30) regimen; all 60 participants completed the study, with no loss-to-follow-up. Mean total HIV DNA at weeks 16 and 18 after randomisation was 3·02 log10 copies HIV DNA per 106 CD4+ T-cells in the ART-only group versus 3·06 log10 copies HIV DNA per 106 CD4+ T-cells in ART + V + V group, with no statistically significant difference between the two groups (mean difference of 0·04 log10 copies HIV DNA per 106 CD4+ T-cells [95% CI -0·03 to 0·11; p=0·26]). There were no intervention-related serious adverse events.Interpretation: This kick and kill approach conferred no significant benefit compared with ART alone on measures of the HIV reservoir. Although this does not disprove the efficacy kick and kill strategy, for future trials enhancement of both kick and kill agents will be required.Funding: Medical Research Council (MR/L00528X/1). [ABSTRACT FROM AUTHOR] - Abstract: Copyright of Lancet is the property of Lancet and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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