<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martin-Otal C</submitter><funding>CARAMBA</funding><funding>AUTOCART</funding><funding>Paula &amp;amp; Rodger Riney Foundation</funding><funding>European Union</funding><funding>Ministerio de Ciencia e Innovación</funding><funding>Hepacare Project</funding><funding>Gobierno de Navarra Industria</funding><funding>Fundación Bancaria La Caixa</funding><pagination>e004479</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9351345</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>One of the main difficulties of adoptive cell therapies with chimeric antigen receptor (CAR)-T cells in solid tumors is the identification of specific target antigens. The tumor microenvironment can present suitable antigens for CAR design, even though they are not expressed by the tumor cells. We have generated a CAR specific for the splice variant extra domain A (EDA) of fibronectin, which is highly expressed in the tumor stroma of many types of tumors but not in healthy tissues.&lt;h4>Methods&lt;/h4>EDA expression was explored in RNA-seq data from different human tumor types and by immunohistochemistry in paraffin-embedded tumor biopsies. Murine and human anti-EDA CAR-T cells were prepared using recombinant retro/lentiviruses, respectively. The functionality of EDA CAR-T ce</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>Targeting the extra domain A of fibronectin for cancer therapy with CAR-T cells.</pubmed_title><pmcid>PMC9351345</pmcid><funding_grant_id>H2020-JTI-IMI2-2019-18</funding_grant_id><funding_grant_id>T2EVOLVE</funding_grant_id><funding_grant_id>MCIN/AEI/10.13039</funding_grant_id><funding_grant_id>945393</funding_grant_id><funding_grant_id>IJCI-2017-34204</funding_grant_id><funding_grant_id>PID2021-128283OA-I00</funding_grant_id><funding_grant_id>SC1-PM-08-2017</funding_grant_id><funding_grant_id>0011-1411-2019-000079, DESCARTHeS</funding_grant_id><funding_grant_id>PLEC2021-008094</funding_grant_id><funding_grant_id>PID2019-108989RB-I00</funding_grant_id><funding_grant_id>0011-1411-2022-000088, SOCRATHeS</funding_grant_id><funding_grant_id>501100011033</funding_grant_id><funding_grant_id>RTC-2017-6585-1</funding_grant_id><funding_grant_id>754658</funding_grant_id><pubmed_authors>Conde E</pubmed_authors><pubmed_authors>Casares N</pubmed_authors><pubmed_authors>De Andrea CE</pubmed_authors><pubmed_authors>Hervas-Stubbs S</pubmed_authors><pubmed_authors>Gorraiz M</pubmed_authors><pubmed_authors>Martin-Otal C</pubmed_authors><pubmed_authors>Sarrion P</pubmed_authors><pubmed_authors>Lasarte-Cia A</pubmed_authors><pubmed_authors>Vilas A</pubmed_authors><pubmed_authors>Prosper F</pubmed_authors><pubmed_authors>San Miguel J</pubmed_authors><pubmed_authors>Serrano D</pubmed_authors><pubmed_authors>Echeveste J</pubmed_authors><pubmed_authors>Calvo A</pubmed_authors><pubmed_authors>Lasarte JJ</pubmed_authors><pubmed_authors>Lozano T</pubmed_authors><pubmed_authors>Navarro F</pubmed_authors><pubmed_authors>Rodriguez-Madoz JR</pubmed_authors><pubmed_authors>Sanchez-Moreno I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting the extra domain A of fibronectin for cancer therapy with CAR-T cells.</name><description>&lt;h4>Background&lt;/h4>One of the main difficulties of adoptive cell therapies with chimeric antigen receptor (CAR)-T cells in solid tumors is the identification of specific target antigens. The tumor microenvironment can present suitable antigens for CAR design, even though they are not expressed by the tumor cells. We have generated a CAR specific for the splice variant extra domain A (EDA) of fibronectin, which is highly expressed in the tumor stroma of many types of tumors but not in healthy tissues.&lt;h4>Methods&lt;/h4>EDA expression was explored in RNA-seq data from different human tumor types and by immunohistochemistry in paraffin-embedded tumor biopsies. Murine and human anti-EDA CAR-T cells were prepared using recombinant retro/lentiviruses, respectively. The functionality of EDA CAR-T ce</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-07-14T17:15:59.513Z</modification><creation>2026-06-21T03:13:07.408Z</creation></dates><accession>S-EPMC9351345</accession><cross_references><pubmed>35918123</pubmed><doi>10.1136/jitc-2021-004479</doi></cross_references></HashMap>