<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Maruta M</submitter><funding>MEXT | Japan Society for the Promotion of Science</funding><funding>Uehara Memorial Foundation</funding><pagination>13293</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6746725</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>The development of chimeric antigen receptor (CAR) and bispecific T-cell engager (BiTE) has led to the successful application of cancer immunotherapy. The potential reactivity mediated by CAR- and BiTE-redirected T cells needs to be assessed to facilitate the application of these treatment options to a broader range of patients. Here, we have generated CAR and BiTE possessing the same single chain fragment variable (scFv) specific for the HLA-A2/NY-ESO-1&lt;sub>157-165&lt;/sub> complex (A2/NY-ESO-1&lt;sub>157&lt;/sub>). Using HLA-A2&lt;sup>+&lt;/sup>NY-ESO-1&lt;sup>+&lt;/sup> myeloma cells and peptides presented by HLA-A2 molecules as a model, both sets of redirected T cells recognized and killed HLA-A2&lt;sup>+&lt;/sup>NY-ESO-1&lt;sup>+&lt;/sup> myeloma cells in an A2/NY-ESO-1&lt;sub>157&lt;/sub>-specific manner in vitro. Moreove</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Direct comparison of target-reactivity and cross-reactivity induced by CAR- and BiTE-redirected T cells for the development of antibody-based T-cell therapy.</pubmed_title><pmcid>PMC6746725</pmcid><funding_grant_id>JP16H07025</funding_grant_id><funding_grant_id>JP18H02839</funding_grant_id><pubmed_authors>Saitou T</pubmed_authors><pubmed_authors>Takenaka K</pubmed_authors><pubmed_authors>Maruta M</pubmed_authors><pubmed_authors>Tanimoto K</pubmed_authors><pubmed_authors>Ochi T</pubmed_authors><pubmed_authors>Fujiwara H</pubmed_authors><pubmed_authors>Yasukawa M</pubmed_authors><pubmed_authors>Imamura T</pubmed_authors><pubmed_authors>Asai H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Direct comparison of target-reactivity and cross-reactivity induced by CAR- and BiTE-redirected T cells for the development of antibody-based T-cell therapy.</name><description>The development of chimeric antigen receptor (CAR) and bispecific T-cell engager (BiTE) has led to the successful application of cancer immunotherapy. The potential reactivity mediated by CAR- and BiTE-redirected T cells needs to be assessed to facilitate the application of these treatment options to a broader range of patients. Here, we have generated CAR and BiTE possessing the same single chain fragment variable (scFv) specific for the HLA-A2/NY-ESO-1&lt;sub>157-165&lt;/sub> complex (A2/NY-ESO-1&lt;sub>157&lt;/sub>). Using HLA-A2&lt;sup>+&lt;/sup>NY-ESO-1&lt;sup>+&lt;/sup> myeloma cells and peptides presented by HLA-A2 molecules as a model, both sets of redirected T cells recognized and killed HLA-A2&lt;sup>+&lt;/sup>NY-ESO-1&lt;sup>+&lt;/sup> myeloma cells in an A2/NY-ESO-1&lt;sub>157&lt;/sub>-specific manner in vitro. Moreove</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Sep</publication><modification>2025-04-22T06:17:53.044Z</modification><creation>2019-10-11T07:05:47Z</creation></dates><accession>S-EPMC6746725</accession><cross_references><pubmed>31527633</pubmed><doi>10.1038/s41598-019-49834-2</doi></cross_references></HashMap>