<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Holanda RA</submitter><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico</funding><pagination>e0005927</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5627964</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(9)</volume><pubmed_abstract>Paracoccidioidomycosis (PCM) is an infectious disease endemic to South America, caused by the thermally dimorphic fungi Paracoccidioides. Currently, there is no effective human vaccine that can be used in prophylactic or therapeutic regimes. We tested the hypothesis that the immunogenicity of the immunodominant CD4+ T-cell epitope (P10) of Paracoccidioides brasiliensis gp43 antigen might be significantly enhanced by using a hepatitis B virus-derived particle (VLP) as an antigen carrier. This chimera was administered to mice as a (His)6-purified protein (rPbT) or a replication-deficient human type 5 adenoviral vector (rAdPbT) in an immunoprophylaxis assay. The highly virulent Pb18 yeast strain was used to challenge our vaccine candidates. Fungal challenge evoked robust P10-specific memory C</pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pubmed_title>Recombinant vaccines of a CD4+ T-cell epitope promote efficient control of Paracoccidioides brasiliensis burden by restraining primary organ infection.</pubmed_title><pmcid>PMC5627964</pmcid><funding_grant_id>142659/2011-8</funding_grant_id><pubmed_authors>Dias LS</pubmed_authors><pubmed_authors>Santos JRA</pubmed_authors><pubmed_authors>Holanda RA</pubmed_authors><pubmed_authors>Silva LBR</pubmed_authors><pubmed_authors>Munoz JE</pubmed_authors><pubmed_authors>Bruna-Romero O</pubmed_authors><pubmed_authors>Santos DA</pubmed_authors><pubmed_authors>Pagliari S</pubmed_authors><pubmed_authors>Taborda CP</pubmed_authors><pubmed_authors>Vieira ELM</pubmed_authors><pubmed_authors>Paixao TA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recombinant vaccines of a CD4+ T-cell epitope promote efficient control of Paracoccidioides brasiliensis burden by restraining primary organ infection.</name><description>Paracoccidioidomycosis (PCM) is an infectious disease endemic to South America, caused by the thermally dimorphic fungi Paracoccidioides. Currently, there is no effective human vaccine that can be used in prophylactic or therapeutic regimes. We tested the hypothesis that the immunogenicity of the immunodominant CD4+ T-cell epitope (P10) of Paracoccidioides brasiliensis gp43 antigen might be significantly enhanced by using a hepatitis B virus-derived particle (VLP) as an antigen carrier. This chimera was administered to mice as a (His)6-purified protein (rPbT) or a replication-deficient human type 5 adenoviral vector (rAdPbT) in an immunoprophylaxis assay. The highly virulent Pb18 yeast strain was used to challenge our vaccine candidates. Fungal challenge evoked robust P10-specific memory C</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Sep</publication><modification>2025-04-20T03:37:14.714Z</modification><creation>2019-03-27T02:58:12Z</creation></dates><accession>S-EPMC5627964</accession><cross_references><pubmed>28938005</pubmed><doi>10.1371/journal.pntd.0005927</doi></cross_references></HashMap>