The Effects of Human Immunodeficiency Virus Type 1 (HIV-1) Antigen-Expanded Specific T-Cell Therapy and Vorinostat on Persistent HIV-1 Infection in People With HIV on Antiretroviral Therapy

被引:4
|
作者
Gay, Cynthia L. [1 ,2 ]
Hanley, Patrick J. [3 ,4 ]
Falcinelli, Shane D. [1 ,2 ,5 ]
Kuruc, JoAnn D. [1 ,2 ]
Pedersen, Susan M. [1 ,2 ]
Kirchherr, Jennifer [1 ,2 ]
Raines, Samuel L. M. [1 ]
Motta, Cecilia M. [3 ]
Lazarski, Chris [3 ,4 ]
Chansky, Pamela [3 ]
Tanna, Jay [3 ]
Shibli, Abeer [3 ]
Datar, Anushree [3 ]
McCann, Chase D. [3 ,4 ]
Sili, Uluhan [3 ]
Ke, Ruian [6 ]
Eron, Joseph J. [1 ,7 ]
Archin, Nancie [1 ,2 ]
Goonetilleke, Nilu [1 ,5 ]
Bollard, Catherine M. [3 ]
Margolis, David M. [1 ,2 ,5 ,7 ]
机构
[1] Univ N Carolina, UNC HIV Cure Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, 2016 Genet Med Bldg,120 Mason Farm Rd,CB 7042, Chapel Hill, NC 27599 USA
[3] Childrens Natl Hlth Syst, Ctr Canc & Immunol Res, Washington, DC USA
[4] George Washington Univ, Pediat & GW Canc Ctr, Washington, DC USA
[5] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[6] Los Alamos Natl Lab, Theoret Biol & Biophys Grp, Los Alamos, NM USA
[7] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2024年 / 229卷 / 03期
基金
美国国家卫生研究院;
关键词
HIV latency; T-cell therapy; latency reversal; LATENT RESERVOIR; TARGET;
D O I
10.1093/infdis/jiad423
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background The histone deacetylase inhibitor vorinostat (VOR) can reverse human immunodeficiency virus type 1 (HIV-1) latency in vivo and allow T cells to clear infected cells in vitro. HIV-specific T cells (HXTCs) can be expanded ex vivo and have been safely administered to people with HIV (PWH) on antiretroviral therapy.Methods Six PWH received infusions of 2 x 107 HXTCs/m(2) with VOR 400 mg, and 3 PWH received infusions of 10 x 107 HXTCs/m(2) with VOR. The frequency of persistent HIV by multiple assays including quantitative viral outgrowth assay (QVOA) of resting CD4+ T cells was measured before and after study therapy.Results VOR and HXTCs were safe, and biomarkers of serial VOR effect were detected, but enhanced antiviral activity in circulating cells was not evident. After 2 x 107 HXTCs/m(2) with VOR, 1 of 6 PWH exhibited a decrease in QVOA, and all 3 PWH exhibited such declines after 10 x 107 HXTCs/m(2) and VOR. However, most declines did not exceed the 6-fold threshold needed to definitively attribute decline to the study intervention.Conclusions These modest effects provide support for the strategy of HIV latency reversal and reservoir clearance, but more effective interventions are needed to yield the profound depletion of persistent HIV likely to yield clinical benefit. Clinical Trials Registration. NCT03212989.Conclusions These modest effects provide support for the strategy of HIV latency reversal and reservoir clearance, but more effective interventions are needed to yield the profound depletion of persistent HIV likely to yield clinical benefit. Clinical Trials Registration. NCT03212989. The HIV latency reversal agent vorinostat was well tolerated when given with expanded, autologous, HIV-specific cytotoxic T cells, but only modest effects were seen on the pool of latently infected cells that persist in people with HIV on therapy.
引用
收藏
页码:743 / 752
页数:10
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