<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Godinho RM</submitter><funding>NIAID NIH HHS</funding><pagination>e99887</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4059647</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(6)</volume><pubmed_abstract>We have previously demonstrated that a DNA vaccine encoding HIV-p55gag in association with the lysosomal associated membrane protein-1 (LAMP-1) elicited a greater Gag-specific immune response, in comparison to a DNA encoding the native gag. In vitro studies have also demonstrated that LAMP/Gag was highly expressed and was present in MHCII containing compartments in transfected cells. In this study, the mechanisms involved in these processes and the relative contributions of the increased expression and altered traffic for the enhanced immune response were addressed. Cells transfected with plasmid DNA constructs containing p55gag attached to truncated sequences of LAMP-1 showed that the increased expression of gag mRNA required p55gag in frame with at least 741 bp of the LAMP-1 luminal doma</pubmed_abstract><journal>PloS one</journal><pubmed_title>Regulation of HIV-Gag expression and targeting to the endolysosomal/secretory pathway by the luminal domain of lysosomal-associated membrane protein (LAMP-1) enhance Gag-specific immune response.</pubmed_title><pmcid>PMC4059647</pmcid><funding_grant_id>R37-AI41908</funding_grant_id><funding_grant_id>R21-AI44317</funding_grant_id><funding_grant_id>R37 AI041908</funding_grant_id><pubmed_authors>Matassoli FL</pubmed_authors><pubmed_authors>Goncalves JL</pubmed_authors><pubmed_authors>Pecanha LM</pubmed_authors><pubmed_authors>Maciel M</pubmed_authors><pubmed_authors>Lucas CG</pubmed_authors><pubmed_authors>Rigato PO</pubmed_authors><pubmed_authors>Sato MN</pubmed_authors><pubmed_authors>de Arruda LB</pubmed_authors><pubmed_authors>Marques ET</pubmed_authors><pubmed_authors>August JT</pubmed_authors><pubmed_authors>Godinho RM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Regulation of HIV-Gag expression and targeting to the endolysosomal/secretory pathway by the luminal domain of lysosomal-associated membrane protein (LAMP-1) enhance Gag-specific immune response.</name><description>We have previously demonstrated that a DNA vaccine encoding HIV-p55gag in association with the lysosomal associated membrane protein-1 (LAMP-1) elicited a greater Gag-specific immune response, in comparison to a DNA encoding the native gag. In vitro studies have also demonstrated that LAMP/Gag was highly expressed and was present in MHCII containing compartments in transfected cells. In this study, the mechanisms involved in these processes and the relative contributions of the increased expression and altered traffic for the enhanced immune response were addressed. Cells transfected with plasmid DNA constructs containing p55gag attached to truncated sequences of LAMP-1 showed that the increased expression of gag mRNA required p55gag in frame with at least 741 bp of the LAMP-1 luminal doma</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2026-04-07T16:41:17.028Z</modification><creation>2019-03-26T23:24:55Z</creation></dates><accession>S-EPMC4059647</accession><cross_references><pubmed>24932692</pubmed><doi>10.1371/journal.pone.0099887</doi></cross_references></HashMap>