<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(4)</volume><submitter>Fournier N</submitter><pubmed_abstract>Plasmacytoid dendritic cells (pDCs) play a central role for both innate and adaptive antiviral responses, as they direct immune responses through their unique ability to produce substantial concentrations of type I interferon (IFNs) upon viral encounter while also activating multiple immune cells, including macrophages, DCs, B, natural killer and T cells. Recent evidence clearly indicates that pDCs also play a crucial role in some cancers and several auto-immune diseases. Although treatments are currently available to patients with such pathologies, many are not fully efficient. We are proposing here, as a new targeted-based therapy, a novel chimeric monoclonal antibody (mAb) that mediates a strong cellular cytotoxicity directed against a specific human pDC marker, CD303. This antibody, ch</pubmed_abstract><journal>mAbs</journal><pagination>651-663</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5973763</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Improved in vitro and in vivo activity against CD303-expressing targets of the chimeric 122A2 antibody selected for specific glycosylation pattern.</pubmed_title><pmcid>PMC5973763</pmcid><pubmed_authors>Derache D</pubmed_authors><pubmed_authors>Fournier N</pubmed_authors><pubmed_authors>Jacque E</pubmed_authors><pubmed_authors>Fontayne A</pubmed_authors><pubmed_authors>Longue A</pubmed_authors><pubmed_authors>Dupont G</pubmed_authors><pubmed_authors>Dezetter AS</pubmed_authors><pubmed_authors>Baptista L</pubmed_authors><pubmed_authors>Dehenne A</pubmed_authors><pubmed_authors>Verhaeghe L</pubmed_authors><pubmed_authors>Pochet-Beghin V</pubmed_authors><pubmed_authors>Chtourou S</pubmed_authors><pubmed_authors>Terrier A</pubmed_authors><pubmed_authors>Beghin C</pubmed_authors><pubmed_authors>de Romeuf C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Improved in vitro and in vivo activity against CD303-expressing targets of the chimeric 122A2 antibody selected for specific glycosylation pattern.</name><description>Plasmacytoid dendritic cells (pDCs) play a central role for both innate and adaptive antiviral responses, as they direct immune responses through their unique ability to produce substantial concentrations of type I interferon (IFNs) upon viral encounter while also activating multiple immune cells, including macrophages, DCs, B, natural killer and T cells. Recent evidence clearly indicates that pDCs also play a crucial role in some cancers and several auto-immune diseases. Although treatments are currently available to patients with such pathologies, many are not fully efficient. We are proposing here, as a new targeted-based therapy, a novel chimeric monoclonal antibody (mAb) that mediates a strong cellular cytotoxicity directed against a specific human pDC marker, CD303. This antibody, ch</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 May/Jun</publication><modification>2025-04-05T15:06:01.769Z</modification><creation>2019-03-26T23:39:34Z</creation></dates><accession>S-EPMC5973763</accession><cross_references><pubmed>29553870</pubmed><doi>10.1080/19420862.2018.1451283</doi></cross_references></HashMap>