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      Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1

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          Abstract

          Reactivation of HIV gene expression in latently infected cells together with an efficient cART has been proposed as an adjuvant therapy aimed at eliminating/decreasing the reservoir size. Results from HIV clinical trials using deacetylase inhibitors ( HDACIs) question the efficiency of these latency‐reversing agents ( LRAs) used alone and underline the need to evaluate other LRAs in combination with HDACIs. Here, we evaluated the therapeutic potential of a demethylating agent (5‐AzadC) in combination with clinically tolerable HDACIs in reactivating HIV‐1 from latency first in vitro and next ex vivo. We showed that a sequential treatment with 5‐AzadC and HDACIs was more effective than the corresponding simultaneous treatment both in vitro and ex vivo. Interestingly, only two of the sequential LRA combinatory treatments tested induced HIV‐1 particle recovery in a higher manner than the drugs alone ex vivo and at concentrations lower than the human tolerable plasmatic concentrations. Taken together, our data reveal the benefit of using combinations of 5‐AzadC with an HDACI and, for the first time, the importance of treatment time schedule for LRA combinations in order to reactivate HIV.

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          HIV reproducibly establishes a latent infection after acute infection of T cells in vitro.

          The presence of latent reservoirs has prevented the eradication of human immunodeficiency virus (HIV) from infected patients successfully treated with anti-retroviral therapy. The mechanism of postintegration latency is poorly understood, partly because of the lack of an in vitro model. We have used an HIV retroviral vector or a full-length HIV genome expressing green fluorescent protein to infect a T lymphocyte cell line in vitro and highly enrich for latently infected cells. HIV latency occurred reproducibly, albeit with low frequency, during an acute infection. Clonal cell lines derived from latent populations showed no detectable basal expression, but could be transcriptionally activated after treatment with phorbol esters or tumor necrosis factor alpha. Direct sequencing of integration sites demonstrated that latent clones frequently contain HIV integrated in or close to alphoid repeat elements in heterochromatin. This is in contrast to a productive infection where integration in or near heterochromatin is disfavored. These observations demonstrate that HIV can reproducibly establish a latent infection as a consequence of integration in or near heterochromatin.
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            Decitabine improves patient outcomes in myelodysplastic syndromes: results of a phase III randomized study.

            Aberrant DNA methylation, which results in leukemogenesis, is frequent in patients with myelodysplastic syndromes (MDS) and is a potential target for pharmacologic therapy. Decitabine indirectly depletes methylcytosine and causes hypomethylation of target gene promoters. A total of 170 patients with MDS were randomized to receive either decitabine at a dose of 15 mg/m2 given intravenously over 3 hours every 8 hours for 3 days (at a dose of 135 mg/m2 per course) and repeated every 6 weeks, or best supportive care. Response was assessed using the International Working Group criteria and required that response criteria be met for at least 8 weeks. Patients who were treated with decitabine achieved a significantly higher overall response rate (17%), including 9% complete responses, compared with supportive care (0%) (P < .001). An additional 12 patients who were treated with decitabine (13%) achieved hematologic improvement. Responses were durable (median, 10.3 mos) and were associated with transfusion independence. Patients treated with decitabine had a trend toward a longer median time to acute myelogenous leukemia (AML) progression or death compared with patients who received supportive care alone (all patients, 12.1 mos vs. 7.8 mos [P = 0.16]; those with International Prognostic Scoring System intermediate-2/high-risk disease, 12.0 mos vs. 6.8 mos [P = 0.03]; those with de novo disease, 12.6 mos vs. 9.4 mos [P = 0.04]; and treatment-naive patients, 12.3 mos vs. 7.3 mos [P = 0.08]). Decitabine was found to be clinically effective in the treatment of patients with MDS, provided durable responses, and improved time to AML transformation or death. The duration of decitabine therapy may improve these results further. 2006 American Cancer Society
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              The Depsipeptide Romidepsin Reverses HIV-1 Latency In Vivo

              Pharmacologically-induced activation of replication competent proviruses from latency in the presence of antiretroviral treatment (ART) has been proposed as a step towards curing HIV-1 infection. However, until now, approaches to reverse HIV-1 latency in humans have yielded mixed results. Here, we report a proof-of-concept phase Ib/IIa trial where 6 aviremic HIV-1 infected adults received intravenous 5 mg/m2 romidepsin (Celgene) once weekly for 3 weeks while maintaining ART. Lymphocyte histone H3 acetylation, a cellular measure of the pharmacodynamic response to romidepsin, increased rapidly (maximum fold range: 3.7–7.7 relative to baseline) within the first hours following each romidepsin administration. Concurrently, HIV-1 transcription quantified as copies of cell-associated un-spliced HIV-1 RNA increased significantly from baseline during treatment (range of fold-increase: 2.4–5.0; p = 0.03). Plasma HIV-1 RNA increased from <20 copies/mL at baseline to readily quantifiable levels at multiple post-infusion time-points in 5 of 6 patients (range 46–103 copies/mL following the second infusion, p = 0.04). Importantly, romidepsin did not decrease the number of HIV-specific T cells or inhibit T cell cytokine production. Adverse events (all grade 1–2) were consistent with the known side effects of romidepsin. In conclusion, romidepsin safely induced HIV-1 transcription resulting in plasma HIV-1 RNA that was readily detected with standard commercial assays demonstrating that significant reversal of HIV-1 latency in vivo is possible without blunting T cell-mediated immune responses. These finding have major implications for future trials aiming to eradicate the HIV-1 reservoir. Trial Registration clinicaltrials.gov NTC02092116
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                Author and article information

                Journal
                EMBO Mol Med
                EMBO Mol Med
                10.1002/(ISSN)1757-4684
                EMMM
                embomm
                EMBO Molecular Medicine
                John Wiley and Sons Inc. (Hoboken )
                1757-4676
                1757-4684
                17 December 2015
                February 2016
                : 8
                : 2 ( doiID: 10.1002/emmm.v8.2 )
                : 117-138
                Affiliations
                [ 1 ] Service of Molecular Virology Department of Molecular Biology (DBM)Université Libre de Bruxelles (ULB) GosseliesBelgium
                [ 2 ] Service des Maladies Infectieuses Centre Hospitalier Universitaire (CHU) de Liège Domaine Universitaire du Sart‐TilmanUniversité de Liège LiègeBelgium
                [ 3 ] Laboratory of Immunology IRISLab CHU‐BrugmannUniversité Libre de Bruxelles (ULB) BrusselsBelgium
                [ 4 ] Service de Virologie EA7327 AP‐HP Hôpital Necker‐Enfants‐MaladesUniversité Paris‐Descartes ParisFrance
                [ 5 ] Service des Maladies Infectieuses CHU St‐PierreUniversité Libre de Bruxelles (ULB) BrusselsBelgium
                [ 6 ] IUT Louis Pasteur de SchiltigheimUniversity of Strasbourg SchiltigheimFrance
                [ 7 ]Institut Universitaire de France (IUF) ParisFrance
                [ 8 ] Service de Génétique Centre Hospitalier Universitaire (CHU) de LiègeDomaine Universitaire du Sart‐Tilman LiègeBelgium
                Author notes
                [*] [* ]Corresponding author. Tel: +32 2 650 98 07; Fax: +32 2 650 98 00; E‐mail: cvlint@ 123456ulb.ac.be
                Article
                EMMM201505557
                10.15252/emmm.201505557
                4734845
                26681773
                7f813ece-d5aa-49b6-988a-4c9fe470dd85
                © 2015 The Authors. Published under the terms of the CC BY 4.0 license

                This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 June 2015
                : 06 November 2015
                : 09 November 2015
                Page count
                Pages: 22
                Funding
                Funded by: Belgian Fund for Scientific Research (FRS‐FNRS, Belgium)
                Funded by: ANRS (France Recherche Nord&Sud Sida‐HIV Hépatites)
                Funded by: “Fondation Roi Baudouin”
                Funded by: NEAT Program
                Funded by: Walloon Region
                Funded by: “Institut Universitaire de France (IUF)”
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                emmm201505557
                February 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.7.6 mode:remove_FC converted:01.02.2016

                Molecular medicine
                demethylating agent,epigenetics,hdacis,hiv latency,hiv reservoir,microbiology, virology & host pathogen interaction,pharmacology & drug discovery

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