<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kavunja HW</submitter><funding>National Cancer Institute (US)</funding><funding>NCI NIH HHS</funding><pagination>451-460</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5470645</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>66(4)</volume><pubmed_abstract>Cytotoxic T lymphocyte (CTL) can have remarkable abilities to kill tumor cells. However, the establishment of successful CTL-based anticancer therapy has met with many challenges. Within tumor cells, there exist subpopulations with low or no expression of the targeted antigen (termed as antigen-loss variants). In addition, tumor cells can downregulate the levels of major histocompatibility complex class I (MHC-I) molecules on cell surface due to immune pressure. As a result, some tumor cells can escape the immune pressure bestowed by CTLs, resulting in treatment failure. To address these difficulties, a new approach is developed to deliver foreign high-affinity CTL epitopes to tumor tissues utilizing pH-responsive "smart" microparticles (MPs). These MPs could encapsulate CTL peptide epitop</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>Delivery of foreign cytotoxic T lymphocyte epitopes to tumor tissues for effective antitumor immunotherapy against pre-established solid tumors in mice.</pubmed_title><pmcid>PMC5470645</pmcid><funding_grant_id>R01CA149451</funding_grant_id><funding_grant_id>R01 CA149451</funding_grant_id><pubmed_authors>Kavunja HW</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Lang S</pubmed_authors><pubmed_authors>Sungsuwan S</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Delivery of foreign cytotoxic T lymphocyte epitopes to tumor tissues for effective antitumor immunotherapy against pre-established solid tumors in mice.</name><description>Cytotoxic T lymphocyte (CTL) can have remarkable abilities to kill tumor cells. However, the establishment of successful CTL-based anticancer therapy has met with many challenges. Within tumor cells, there exist subpopulations with low or no expression of the targeted antigen (termed as antigen-loss variants). In addition, tumor cells can downregulate the levels of major histocompatibility complex class I (MHC-I) molecules on cell surface due to immune pressure. As a result, some tumor cells can escape the immune pressure bestowed by CTLs, resulting in treatment failure. To address these difficulties, a new approach is developed to deliver foreign high-affinity CTL epitopes to tumor tissues utilizing pH-responsive "smart" microparticles (MPs). These MPs could encapsulate CTL peptide epitop</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2025-04-19T17:33:47.24Z</modification><creation>2025-04-19T17:33:47.24Z</creation></dates><accession>S-EPMC5470645</accession><cross_references><pubmed>28011995</pubmed><doi>10.1007/s00262-016-1948-9</doi></cross_references></HashMap>