<HashMap><database>biostudies-literature</database><scores/><additional><submitter>van Osch TLJ</submitter><funding>PPOC grant from Stichting Sanquin bloedvoorziening</funding><pagination>3011-3025</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9828502</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The formation of alloantibodies directed against class I human leukocyte antigens (HLA) continues to be a clinically challenging complication after platelet transfusions, which can lead to platelet refractoriness (PR) and occurs in approximately 5%-15% of patients with chronic platelet support. Interestingly, anti-HLA IgG levels in alloimmunized patients do not seem to predict PR, suggesting functional or qualitative differences among anti-HLA IgG. The binding of these alloantibodies to donor platelets can result in rapid clearance after transfusion, presumably via FcγR-mediated phagocytosis and/or complement activation, which both are affected by the IgG-Fc glycosylation.&lt;h4>Objectives&lt;/h4>To characterize the Fc glycosylation profile of anti-HLA class I antibodies forme</pubmed_abstract><journal>Journal of thrombosis and haemostasis : JTH</journal><pubmed_title>Altered Fc glycosylation of anti-HLA alloantibodies in hemato-oncological patients receiving platelet transfusions.</pubmed_title><pmcid>PMC9828502</pmcid><funding_grant_id>2282</funding_grant_id><pubmed_authors>Geerdes DM</pubmed_authors><pubmed_authors>Pongracz T</pubmed_authors><pubmed_authors>Vidarsson G</pubmed_authors><pubmed_authors>Kerkhoffs JH</pubmed_authors><pubmed_authors>de Haas M</pubmed_authors><pubmed_authors>Wuhrer M</pubmed_authors><pubmed_authors>van Osch TLJ</pubmed_authors><pubmed_authors>Kapur R</pubmed_authors><pubmed_authors>Mok JY</pubmed_authors><pubmed_authors>Porcelijn L</pubmed_authors><pubmed_authors>van der Meer PF</pubmed_authors><pubmed_authors>Voorberg J</pubmed_authors><pubmed_authors>van der Schoot CE</pubmed_authors><pubmed_authors>van Esch WJE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Altered Fc glycosylation of anti-HLA alloantibodies in hemato-oncological patients receiving platelet transfusions.</name><description>&lt;h4>Background&lt;/h4>The formation of alloantibodies directed against class I human leukocyte antigens (HLA) continues to be a clinically challenging complication after platelet transfusions, which can lead to platelet refractoriness (PR) and occurs in approximately 5%-15% of patients with chronic platelet support. Interestingly, anti-HLA IgG levels in alloimmunized patients do not seem to predict PR, suggesting functional or qualitative differences among anti-HLA IgG. The binding of these alloantibodies to donor platelets can result in rapid clearance after transfusion, presumably via FcγR-mediated phagocytosis and/or complement activation, which both are affected by the IgG-Fc glycosylation.&lt;h4>Objectives&lt;/h4>To characterize the Fc glycosylation profile of anti-HLA class I antibodies forme</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-21T17:58:35.383Z</modification><creation>2025-04-05T17:02:34.429Z</creation></dates><accession>S-EPMC9828502</accession><cross_references><pubmed>36165642</pubmed><doi>10.1111/jth.15898</doi></cross_references></HashMap>