<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3</volume><submitter>Volz B</submitter><pubmed_abstract>The tumor vaccine MGN1601 was designed and developed for treatment of metastatic renal cell carcinoma (mRCC). MGN1601 consists of a combination of fourfold gene-modified cells with the toll-like receptor 9 agonist dSLIM, a powerful connector of innate and adaptive immunity. Vaccine cells originate from a renal cell carcinoma cell line (grown from renal cell carcinoma tissue), express a variety of known tumor-associated antigens (TAA), and are gene modified to transiently express two co-stimulatory molecules, CD80 and CD154, and two cytokines, GM-CSF and IL-7, aimed to support immune response. Proof of concept of the designed vaccine was shown in mice: The murine homologue of the vaccine efficiently (100%) prevented tumor growth when used as prophylactic vaccine in a syngeneic setting. Use </pubmed_abstract><journal>Molecular therapy oncolytics</journal><pagination>15023</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4824560</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Design and characterization of the tumor vaccine MGN1601, allogeneic fourfold gene-modified vaccine cells combined with a TLR-9 agonist.</pubmed_title><pmcid>PMC4824560</pmcid><pubmed_authors>Schmidt M</pubmed_authors><pubmed_authors>Schroff M</pubmed_authors><pubmed_authors>Volz B</pubmed_authors><pubmed_authors>Heinrich K</pubmed_authors><pubmed_authors>Kapp K</pubmed_authors><pubmed_authors>Wittig B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Design and characterization of the tumor vaccine MGN1601, allogeneic fourfold gene-modified vaccine cells combined with a TLR-9 agonist.</name><description>The tumor vaccine MGN1601 was designed and developed for treatment of metastatic renal cell carcinoma (mRCC). MGN1601 consists of a combination of fourfold gene-modified cells with the toll-like receptor 9 agonist dSLIM, a powerful connector of innate and adaptive immunity. Vaccine cells originate from a renal cell carcinoma cell line (grown from renal cell carcinoma tissue), express a variety of known tumor-associated antigens (TAA), and are gene modified to transiently express two co-stimulatory molecules, CD80 and CD154, and two cytokines, GM-CSF and IL-7, aimed to support immune response. Proof of concept of the designed vaccine was shown in mice: The murine homologue of the vaccine efficiently (100%) prevented tumor growth when used as prophylactic vaccine in a syngeneic setting. Use </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-05-05T01:36:40.765Z</modification><creation>2019-03-27T03:11:27Z</creation></dates><accession>S-EPMC4824560</accession><cross_references><pubmed>27119114</pubmed><doi>10.1038/mto.2015.23</doi></cross_references></HashMap>