Fimepinostat, a novel dual inhibitor of HDAC and PI3K, effectively reverses HIV-1 latency ex vivo without T cell activation

Jesper D Gunst; Kathrine Kjær; Rikke Olesen; Thomas A Rasmussen; Lars Østergaard; Paul W Denton; Ole S Søgaard; Martin Tolstrup

Fimepinostat, a novel dual inhibitor of HDAC and PI3K, effectively reverses HIV-1 latency ex vivo without T cell activation

J Virus Erad. 2019 Sep 18;5(3):133-137.

Authors

Jesper D Gunst^{1

2}, Kathrine Kjær^{1

2}, Rikke Olesen^{1

2}, Thomas A Rasmussen^{1

2}, Lars Østergaard^{1

2}, Paul W Denton^{1

2}, Ole S Søgaard^{1

2}, Martin Tolstrup^{1

2}

Affiliations

¹ Department of Infectious Diseases, Aarhus University Hospital, Denmark.
² Institute of Clinical Medicine, Aarhus University, Denmark.

PMID: 31700655
PMCID: PMC6816120

Abstract

Objectives: To test the potential of fimepinostat (CUDC-907), a dual inhibitor of histone deacetylases (HDAC) and phosphatidylinositol-3-kinases (PI3K), to reverse human immunodeficiency virus type 1 (HIV-1) latency in infected cell lines and in CD4+ T cells from HIV-1-infected donors on long-term combination antiretroviral therapy (cART).

Methods: Latently HIV-1-infected J-lat Tat-GFP and ACH-2 cell lines were stimulated with clinically relevant concentrations of fimepinostat using the HDAC inhibitors (HDACi) panobinostat and romidepsin for comparison. Next, CD4+ T cells from donors living with HIV-1 on long-term cART were stimulated ex vivo and cell-associated unspliced HIV-1 RNA was measured to quantify changes in HIV-1 transcription. Finally, the impact of fimepinostat on T cell activation (CD69 expression) and proliferation (Ki67 expression) was determined using peripheral blood mononuclear cells from uninfected donors.

Results: We found fimepinostat to be a potent latency-reversing agent. This was true in two latently infected cell lines as well as ex vivo in CD4+ T cells isolated from donors living with HIV-1. Relative to therapeutic dosing levels, fimepinostat showed latency-reversing potential comparable to romidepsin, which is the most potent HDACi tested in HIV-1 cure-related trials. Interestingly, in contrast to romidepsin, fimepinostat stimulation resulted in decreased T cell activation and had no negative impact on T cell proliferation.

Conclusions: At therapeutic concentration, the dual HDAC and PI3K inhibitor fimepinostat was a potent HIV-1 latency-reversing agent and it did not induce T cell activation and proliferation. The potential of fimepinostat as a latency-reversing agent warrants further investigation.

Keywords: HDACi; HIV; PI3Ki; T cell activation; fimepinostat; latency-reversal agent.

Publication types

Editorial