<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Diaz de Leon JSA</submitter><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1182-1192</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10876040</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(12)</volume><pubmed_abstract>Factors regulating macrophage effector function represent potential targets to optimize the efficacy of antibody-mediated therapies. Macrophages are myeloid cells capable of engulfing and destroying diseased or damaged target cells. Antibodies binding to the target cell surface can engage macrophage Fc gamma receptors (FcγRs) to elicit antibody-dependent cellular phagocytosis (ADCP), a process that contributes to treatments mediated by anti-tumor antibodies. Conversely, macrophage ADCP of apoptotic T cells is also linked to tolerance in the tumor environment. Here we evaluated the role of asparagine(N)-linked glycans in the function of macrophages derived from primary human monocytes. Macrophages treated with kifunensine, an inhibitor of N-glycan processing, exhibited greater target bindin</pubmed_abstract><journal>Glycobiology</journal><pubmed_title>Macrophage N-glycan processing inhibits antibody-dependent cellular phagocytosis.</pubmed_title><pmcid>PMC10876040</pmcid><funding_grant_id>U01 AI148114</funding_grant_id><pubmed_authors>Aguilar I</pubmed_authors><pubmed_authors>Barb AW</pubmed_authors><pubmed_authors>Diaz de Leon JSA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Macrophage N-glycan processing inhibits antibody-dependent cellular phagocytosis.</name><description>Factors regulating macrophage effector function represent potential targets to optimize the efficacy of antibody-mediated therapies. Macrophages are myeloid cells capable of engulfing and destroying diseased or damaged target cells. Antibodies binding to the target cell surface can engage macrophage Fc gamma receptors (FcγRs) to elicit antibody-dependent cellular phagocytosis (ADCP), a process that contributes to treatments mediated by anti-tumor antibodies. Conversely, macrophage ADCP of apoptotic T cells is also linked to tolerance in the tumor environment. Here we evaluated the role of asparagine(N)-linked glycans in the function of macrophages derived from primary human monocytes. Macrophages treated with kifunensine, an inhibitor of N-glycan processing, exhibited greater target bindin</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-04T01:03:17.002Z</modification><creation>2025-04-04T01:03:17.002Z</creation></dates><accession>S-EPMC10876040</accession><cross_references><pubmed>37792857</pubmed><doi>10.1093/glycob/cwad078</doi></cross_references></HashMap>