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    <responseDate>2026-10-15T11:46:47Z</responseDate>
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            <header>
                <identifier>oai:data.mendeley.com/ttgdhfm4gf.2</identifier>
                <datestamp>2024-12-16T10:22:22Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Kim, Woo Sik</dc:creator>
    <dc:title>Immunogenicity and vaccine efficacy of Actinobacillus pleuropneumoniae-derived extracellular vesicles as a novel vaccine candidate</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Actinobacillus pleuropneumoniae (APP) is a significant pathogen in the swine industry, leading to substantial economic losses and highlighting the need for effective vaccines. This study evaluates the potential of APP-derived extracellular vesicles (APP-EVs) as a vaccine candidate compared to the commercial Coglapix vaccine. APP-EVs, isolated using tangential flow filtration (TFF) and cushioned ultracentrifugation, exhibited an average size of 105 nm and a zeta potential of -17.4 mV. These EVs demonstrated high stability under external stressors, such as pH changes and enzymatic exposure and were found to contain 86 major metabolites. Additionally, APP-EVs induced dendritic cell (DC) maturation in a Toll-like receptor 4 (TLR4)-dependent manner without cytotoxicity. APP-EVs predominantly elicited Th1-mediated IgG responses in immunized mice without significant liver and kidney toxicity. Contrarily, unlike Coglapix, which induced stronger Th2-mediated responses and notable toxicity. In addition, APP-EVs triggered robust APP-specific Th1, Th17, and cytotoxic T lymphocyte (CTL) responses and promoted the activation of multifunctional T-cells. Notably, APP-EV immunization enhanced macrophage phagocytosis and improved survival rates in mice challenged with APP infection compared to those treated with Coglapix. These findings suggest that APP-EVs are promising vaccine candidates, capable of inducing potent APP-specific T-cell responses, particularly Th1, Th17, CTL, and multifunctional T-cells, thereby enhancing the protective immune response against APP infection.</dc:description>
    <dc:subject>Infectious Disease</dc:subject>
    <dc:subject>Vaccine</dc:subject>
    <dc:subject>Pig</dc:subject>
    <dc:subject>Dendritic Cell Function</dc:subject>
    <dc:subject>Gram Negative Bacteria</dc:subject>
    <dc:subject>Extracellular Vesicle</dc:subject>
    <dc:contributor>Park, Su Hyun</dc:contributor>
    <dc:contributor>Kim, Yun Hye </dc:contributor>
    <dc:contributor>Lee, Hyeon Jin </dc:contributor>
    <dc:contributor>Han, Jeong Moo </dc:contributor>
    <dc:contributor>Seo, BYoung-Joo </dc:contributor>
    <dc:contributor>Park, Gyeong-Seo </dc:contributor>
    <dc:contributor>Kim, Chonghan</dc:contributor>
    <dc:contributor>Ryu, Young Bae </dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/ttgdhfm4gf.2</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/ttgdhfm4gf.2</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/ttgdhfm4gf</dc:relation>
    <dc:date>2024-12-16T10:22:22Z</dc:date>
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