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  <identifier identifierType="DOI">10.18453/rosdok_id00004407</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Salewski, Inken</creatorName>
      <givenName>Inken</givenName>
      <familyName>Salewski</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1222442876</nameIdentifier>
      <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="https://orcid.org/">https://orcid.org/0000-0002-5738-4696</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Combined immunotherapy approaches in preclinical models of mismatch-repair-deficiency-associated tumorigenesis</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2023</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">500 Natural sciences</subject>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">570 Life science</subject>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">610 Medical sciences Medicine</subject>
  </subjects>
  <dates>
    <date dateType="Created">2023</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00004407</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00004407-6</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">In this thesis, different immunotherapy strategies we employed to combat mismatch-repair-deficient (dMMR) cancer. We used two preclinical mouse models, either having constitutional (Mlh1) or conditional (Msh2) knock out. To prevent resistance development and improve outcome, we focused on combination strategies including whole tumor vaccines, immune checkpoint-inhibitors (α-PD-L1), classical chemotherapy or the Cyclin-dependent kinase inhibitor abemaciclib. By applying different combination strategies, a significant survival benefit was reached in all investigated treatments.</description>
  </descriptions>
</resource>
