Reference : Histone deacetylase mediated transcriptional activation reduces proviral loads in HTL...
Scientific journals : Article
Human health sciences : Oncology
Histone deacetylase mediated transcriptional activation reduces proviral loads in HTLV-1 associated myelopathy/tropical spastic paraparesis patients.
Lezin, Agnes [> >]
Gillet, Nicolas mailto [Université de Liège - ULg > Chimie et bio-industries > Biologie cell. et moléc. >]
Olindo, Stephane [> >]
Signate, Aissatou [> >]
Grandvaux, Nathalie [> >]
Verlaeten, Olivier [> >]
Belrose, Gildas [> >]
de Carvalho Bittencourt, Marcelo [> >]
Hiscott, John [> >]
Asquith, Becca [> >]
Burny, Arsene [> >]
Smadja, Didier [> >]
Cesaire, Raymond [> >]
Willems, Luc mailto [Université de Liège - ULg > Chimie et bio-industries > Biologie cell. et moléc. >]
American Society of Hematology
Yes (verified by ORBi)
[en] Enzyme Inhibitors/pharmacology ; Gene Expression Regulation, Viral/drug effects ; HeLa Cells ; Histone Deacetylase Inhibitors ; Histone Deacetylases/physiology ; Human T-lymphotropic virus 1/growth & development ; Humans ; Jurkat Cells ; Paraparesis, Tropical Spastic/genetics/virology ; Proviruses/growth & development ; Transcriptional Activation/physiology ; Transfection ; Valproic Acid/pharmacology ; Viral Load
[en] Epigenetic modifications of chromatin may play a role in maintaining viral latency and thus persistence of the human T-lymphotropic virus type 1 (HTLV-1), which is responsible for HTLV-associated myelopathy/tropical spastic paraparesis (HAM/TSP). A major determinant of disease progression is increased peripheral blood proviral load (PVL), possibly via the accumulation of infected cells in the central nervous system (CNS) creating a damaging inflammatory response. Current therapeutic approaches that focus on reducing either cell proliferation, viral replication, or tissue invasion are still unsatisfactory. Contrasting with these inhibitory strategies, we evaluated the efficacy of a novel approach aimed, paradoxically, at activating viral gene expression to expose virus-positive cells to the host immune response. We used valproate (VPA), a histone deacetylase inhibitor that has been used for decades as a chronic, safe treatment for epileptic disorders. Based on in vitro and in vivo data, we provide evidence that transient activation of the latent viral reservoir causes its collapse, a process that may alleviate the condition of HAM/TSP. This represents the first such approach to treating HAM/TSP, using gene activation therapy to tilt the host-pathogen balance in favor of an existing antiviral response. This trial is registered at no. NCT00519181.
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