<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(1)</volume><submitter>Kellner C</submitter><pubmed_abstract>Antibody-dependent cell-mediated cytotoxicity (ADCC) mediated through the IgG Fc receptor FcγRIIIa represents a major effector function of many therapeutic antibodies. In an attempt to further enhance natural killer (NK) cell-mediated ADCC, we combined therapeutic antibodies against CD20 and CD38 with recombinant immunoligands against the stimulatory NK cell receptors NKG2D or NKp30. These immunoligands, respectively designated as ULBP2:7D8 and B7-H6:7D8, contained the CD20 scFv 7D8 as a targeting moiety and a cognate ligand for either NKG2D or NKp30 (i.e. ULBP2 and B7-H6, respectively). Both the immunoligands synergistically augmented ADCC in combination with the CD20 antibody rituximab and the CD38 antibody daratumumab. Combinations with ULBP2:7D8 resulted in higher cytotoxicity compared</pubmed_abstract><journal>Oncoimmunology</journal><pagination>e1058459</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4760288</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Enhancing natural killer cell-mediated lysis of lymphoma cells by combining therapeutic antibodies with CD20-specific immunoligands engaging NKG2D or NKp30.</pubmed_title><pmcid>PMC4760288</pmcid><pubmed_authors>Klausz K</pubmed_authors><pubmed_authors>Derer S</pubmed_authors><pubmed_authors>Parren PW</pubmed_authors><pubmed_authors>Kellner C</pubmed_authors><pubmed_authors>Peipp M</pubmed_authors><pubmed_authors>Humpe A</pubmed_authors><pubmed_authors>Kneba M</pubmed_authors><pubmed_authors>Gunther A</pubmed_authors><pubmed_authors>Gramatzki M</pubmed_authors><pubmed_authors>Repp R</pubmed_authors><pubmed_authors>Bruggemann M</pubmed_authors><pubmed_authors>Valerius T</pubmed_authors><pubmed_authors>van de Winkel JG</pubmed_authors><pubmed_authors>Ritgen M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhancing natural killer cell-mediated lysis of lymphoma cells by combining therapeutic antibodies with CD20-specific immunoligands engaging NKG2D or NKp30.</name><description>Antibody-dependent cell-mediated cytotoxicity (ADCC) mediated through the IgG Fc receptor FcγRIIIa represents a major effector function of many therapeutic antibodies. In an attempt to further enhance natural killer (NK) cell-mediated ADCC, we combined therapeutic antibodies against CD20 and CD38 with recombinant immunoligands against the stimulatory NK cell receptors NKG2D or NKp30. These immunoligands, respectively designated as ULBP2:7D8 and B7-H6:7D8, contained the CD20 scFv 7D8 as a targeting moiety and a cognate ligand for either NKG2D or NKp30 (i.e. ULBP2 and B7-H6, respectively). Both the immunoligands synergistically augmented ADCC in combination with the CD20 antibody rituximab and the CD38 antibody daratumumab. Combinations with ULBP2:7D8 resulted in higher cytotoxicity compared</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-05-05T11:41:27.917Z</modification><creation>2019-03-27T02:09:28Z</creation></dates><accession>S-EPMC4760288</accession><cross_references><pubmed>26942070</pubmed><doi>10.1080/2162402x.2015.1058459</doi><doi>10.1080/2162402X.2015.1058459</doi></cross_references></HashMap>