<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Graziano F</submitter><funding>European Commission (EC)</funding><funding>European Commission</funding><pagination>14249</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6155284</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>We have reported that short-term stimulation of primary human monocyte-derived macrophages (MDM) with interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α), i.e. M1 polarization, leads to a significant containment of virus replication. Here we show that M1-MDM restimulation with these cytokines 7 days after infection (M1&lt;sup>2&lt;/sup> MDM) promoted an increased restriction of HIV-1 replication characterized by very low levels of virus production near to undetectable levels. In comparison to control and M1-MDM that were not restimulated, M1&lt;sup>2&lt;/sup> MDM showed a stronger reduction of both total and integrated HIV DNA as well as of viral mRNA expression. M1&lt;sup>2&lt;/sup> MDM were characterized by an upregulated expression of restriction factors acting at the level of reverse transcription </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Reversible Human Immunodeficiency Virus Type-1 Latency in Primary Human Monocyte-Derived Macrophages Induced by Sustained M1 Polarization.</pubmed_title><pmcid>PMC6155284</pmcid><funding_grant_id>305938</funding_grant_id><funding_grant_id>602893</funding_grant_id><pubmed_authors>Accolla RS</pubmed_authors><pubmed_authors>Poli G</pubmed_authors><pubmed_authors>Forlani G</pubmed_authors><pubmed_authors>Graziano F</pubmed_authors><pubmed_authors>Turrini F</pubmed_authors><pubmed_authors>Aimola G</pubmed_authors><pubmed_authors>Vicenzi E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reversible Human Immunodeficiency Virus Type-1 Latency in Primary Human Monocyte-Derived Macrophages Induced by Sustained M1 Polarization.</name><description>We have reported that short-term stimulation of primary human monocyte-derived macrophages (MDM) with interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α), i.e. M1 polarization, leads to a significant containment of virus replication. Here we show that M1-MDM restimulation with these cytokines 7 days after infection (M1&lt;sup>2&lt;/sup> MDM) promoted an increased restriction of HIV-1 replication characterized by very low levels of virus production near to undetectable levels. In comparison to control and M1-MDM that were not restimulated, M1&lt;sup>2&lt;/sup> MDM showed a stronger reduction of both total and integrated HIV DNA as well as of viral mRNA expression. M1&lt;sup>2&lt;/sup> MDM were characterized by an upregulated expression of restriction factors acting at the level of reverse transcription </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Sep</publication><modification>2025-04-07T11:12:43.447Z</modification><creation>2019-03-26T23:57:42Z</creation></dates><accession>S-EPMC6155284</accession><cross_references><pubmed>30250078</pubmed><doi>10.1038/s41598-018-32451-w</doi></cross_references></HashMap>