<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(12)</volume><submitter>Sconocchia G</submitter><pubmed_abstract>The FcγRII (CD32) ligands are IgFc fragments and pentraxins. The existence of additional ligands is unknown. We engineered T cells with human chimeric receptors resulting from the fusion between CD32 extracellular portion and transmembrane CD8α linked to CD28/ζ chain intracellular moiety (CD32-CR). Transduced T cells recognized three breast cancer (BC) and one colon cancer cell line among 15 tested in the absence of targeting antibodies. Sensitive BC cell conjugation with CD32-CR T cells induced CD32 polarization and down-regulation, CD107a release, mutual elimination, and proinflammatory cytokine production unaffected by human IgGs but enhanced by cetuximab. CD32-CR T cells protected immunodeficient mice from subcutaneous growth of MDA-MB-468 BC cells. RNAseq analysis identified a 42 gene</pubmed_abstract><journal>Life science alliance</journal><pagination>e202201590</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9586128</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Direct CD32 T-cell cytotoxicity: implications for breast cancer prognosis and treatment.</pubmed_title><pmcid>PMC9586128</pmcid><pubmed_authors>Buccisano F</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Iezzi G</pubmed_authors><pubmed_authors>Venditti A</pubmed_authors><pubmed_authors>Maurillo L</pubmed_authors><pubmed_authors>Dou J</pubmed_authors><pubmed_authors>Toietta G</pubmed_authors><pubmed_authors>Cesarini V</pubmed_authors><pubmed_authors>Arriga R</pubmed_authors><pubmed_authors>Sconocchia G</pubmed_authors><pubmed_authors>Aureli A</pubmed_authors><pubmed_authors>Silvestris DA</pubmed_authors><pubmed_authors>Lanzilli G</pubmed_authors><pubmed_authors>De Paolis F</pubmed_authors><pubmed_authors>Spagnoli GC</pubmed_authors><pubmed_authors>Caratelli S</pubmed_authors><pubmed_authors>Del Principe MI</pubmed_authors><pubmed_authors>Rezvani K</pubmed_authors><pubmed_authors>Irno Consalvo M</pubmed_authors><pubmed_authors>Sconocchia T</pubmed_authors><pubmed_authors>Baldari S</pubmed_authors><pubmed_authors>Ottaviani A</pubmed_authors><pubmed_authors>Cenciarelli C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Direct CD32 T-cell cytotoxicity: implications for breast cancer prognosis and treatment.</name><description>The FcγRII (CD32) ligands are IgFc fragments and pentraxins. The existence of additional ligands is unknown. We engineered T cells with human chimeric receptors resulting from the fusion between CD32 extracellular portion and transmembrane CD8α linked to CD28/ζ chain intracellular moiety (CD32-CR). Transduced T cells recognized three breast cancer (BC) and one colon cancer cell line among 15 tested in the absence of targeting antibodies. Sensitive BC cell conjugation with CD32-CR T cells induced CD32 polarization and down-regulation, CD107a release, mutual elimination, and proinflammatory cytokine production unaffected by human IgGs but enhanced by cetuximab. CD32-CR T cells protected immunodeficient mice from subcutaneous growth of MDA-MB-468 BC cells. RNAseq analysis identified a 42 gene</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T22:13:35.722Z</modification><creation>2025-02-18T23:59:31.34Z</creation></dates><accession>S-EPMC9586128</accession><cross_references><pubmed>36241426</pubmed><doi>10.26508/lsa.202201590</doi></cross_references></HashMap>