<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blaudszun AR</submitter><funding>National Research Foundation (NRF)</funding><pagination>1295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10143374</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(4)</volume><pubmed_abstract>Adoptive cell transfer (ACT) has shown remarkable therapeutic efficacy against blood cancers such as leukemia and lymphomas, but its effect is still limited due to the lack of well-defined antigens expressed by aberrant cells within tumors, the insufficient trafficking of administered T cells to the tumor sites, as well as immunosuppression induced by the tumor microenvironment (TME). In this study, we propose the adoptive transfer of photosensitizer (PS)-loaded cytotoxic T cells for a combinational photodynamic and cancer immunotherapy. Temoporfin (Foscan&lt;sup>®&lt;/sup>), a clinically applicable porphyrin derivative, was loaded into OT-1 cells (PS-OT-1 cells). The PS-OT-1 cells efficiently produced a large amount of reactive oxygen species (ROS) under visible light irradiation in a culture; </pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Adoptive Transfer of Photosensitizer-Loaded Cytotoxic T Cells for Combinational Photodynamic Therapy and Cancer Immuno-Therapy.</pubmed_title><pmcid>PMC10143374</pmcid><funding_grant_id>NRF-2022M3H4A1A03067401 and 2021R1C1C2005460</funding_grant_id><pubmed_authors>Kim WJ</pubmed_authors><pubmed_authors>Shim MK</pubmed_authors><pubmed_authors>Um W</pubmed_authors><pubmed_authors>Kim K</pubmed_authors><pubmed_authors>Blaudszun AR</pubmed_authors><pubmed_authors>Yoon HY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Adoptive Transfer of Photosensitizer-Loaded Cytotoxic T Cells for Combinational Photodynamic Therapy and Cancer Immuno-Therapy.</name><description>Adoptive cell transfer (ACT) has shown remarkable therapeutic efficacy against blood cancers such as leukemia and lymphomas, but its effect is still limited due to the lack of well-defined antigens expressed by aberrant cells within tumors, the insufficient trafficking of administered T cells to the tumor sites, as well as immunosuppression induced by the tumor microenvironment (TME). In this study, we propose the adoptive transfer of photosensitizer (PS)-loaded cytotoxic T cells for a combinational photodynamic and cancer immunotherapy. Temoporfin (Foscan&lt;sup>®&lt;/sup>), a clinically applicable porphyrin derivative, was loaded into OT-1 cells (PS-OT-1 cells). The PS-OT-1 cells efficiently produced a large amount of reactive oxygen species (ROS) under visible light irradiation in a culture; </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-21T17:25:33.927Z</modification><creation>2025-04-05T16:40:45.471Z</creation></dates><accession>S-EPMC10143374</accession><cross_references><pubmed>37111779</pubmed><doi>10.3390/pharmaceutics15041295</doi></cross_references></HashMap>