<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Digomann D</submitter><funding>Jung Stiftung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Else Kröner-Fresenius-Stiftung</funding><funding>Monika Kutzner Stiftung</funding><pagination>2326</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10136841</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(8)</volume><pubmed_abstract>Immunotherapy has shown promising results in multiple solid tumors and hematological malignancies. However, pancreatic ductal adenocarcinoma (PDAC) has been largely refractory to current clinical immunotherapies. The V-domain Ig suppressor of T-cell activation (VISTA) inhibits T-cell effector function and maintains peripheral tolerance. Here, we determine VISTA expression in nontumorous pancreatic (&lt;i>n&lt;/i> = 5) and PDAC tissue using immunohistochemistry (&lt;i>n&lt;/i> = 76) and multiplex immunofluorescence staining (&lt;i>n&lt;/i> = 67). Additionally, VISTA expression on tumor-infiltrating immune cells and matched blood samples (&lt;i>n&lt;/i> = 13) was measured with multicolor flow cytometry. Further, the effect of recombinant VISTA on T-cell activation was investigated in vitro, and VISTA blockade was t</pubmed_abstract><journal>Cancers</journal><pubmed_title>VISTA Ligation Reduces Antitumor T-Cell Activity in Pancreatic Cancer.</pubmed_title><pmcid>PMC10136841</pmcid><funding_grant_id>SE2980/5-1</funding_grant_id><funding_grant_id>NA</funding_grant_id><pubmed_authors>Strack J</pubmed_authors><pubmed_authors>Distler M</pubmed_authors><pubmed_authors>Plesca I</pubmed_authors><pubmed_authors>Reiche C</pubmed_authors><pubmed_authors>Seifert L</pubmed_authors><pubmed_authors>Beer C</pubmed_authors><pubmed_authors>Schmitz M</pubmed_authors><pubmed_authors>Digomann D</pubmed_authors><pubmed_authors>Seifert AM</pubmed_authors><pubmed_authors>Heiduk M</pubmed_authors><pubmed_authors>Sommer U</pubmed_authors><pubmed_authors>Rupp L</pubmed_authors><pubmed_authors>Nicolaus S</pubmed_authors><pubmed_authors>Weitz J</pubmed_authors></additional><is_claimable>false</is_claimable><name>VISTA Ligation Reduces Antitumor T-Cell Activity in Pancreatic Cancer.</name><description>Immunotherapy has shown promising results in multiple solid tumors and hematological malignancies. However, pancreatic ductal adenocarcinoma (PDAC) has been largely refractory to current clinical immunotherapies. The V-domain Ig suppressor of T-cell activation (VISTA) inhibits T-cell effector function and maintains peripheral tolerance. Here, we determine VISTA expression in nontumorous pancreatic (&lt;i>n&lt;/i> = 5) and PDAC tissue using immunohistochemistry (&lt;i>n&lt;/i> = 76) and multiplex immunofluorescence staining (&lt;i>n&lt;/i> = 67). Additionally, VISTA expression on tumor-infiltrating immune cells and matched blood samples (&lt;i>n&lt;/i> = 13) was measured with multicolor flow cytometry. Further, the effect of recombinant VISTA on T-cell activation was investigated in vitro, and VISTA blockade was t</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-22T05:15:21.046Z</modification><creation>2025-04-05T21:16:36.855Z</creation></dates><accession>S-EPMC10136841</accession><cross_references><pubmed>37190254</pubmed><doi>10.3390/cancers15082326</doi></cross_references></HashMap>