dc.contributor.author
Raftery, Martin J.
dc.contributor.author
Franzén, Alexander Sebastian
dc.contributor.author
Radecke, Clarissa
dc.contributor.author
Boulifa, Abdelhadi
dc.contributor.author
Schönrich, Günther
dc.contributor.author
Stintzing, Sebastian
dc.contributor.author
Blohmer, Jens-Uwe
dc.contributor.author
Pecher, Gabriele
dc.date.accessioned
2024-04-08T13:55:49Z
dc.date.available
2024-04-08T13:55:49Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/42988
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-42702
dc.description.abstract
There is a medical need to develop new and effective therapies against triple-negative breast cancer (TNBC). Chimeric antigen receptor (CAR) natural killer (NK) cells are a promising alternative to CAR-T cell therapy for cancer. A search for a suitable target in TNBC identified CD44v6, an adhesion molecule expressed in lymphomas, leukemias and solid tumors that is implicated in tumorigenesis and metastases. We have developed a next-generation CAR targeting CD44v6 that incorporates IL-15 superagonist and checkpoint inhibitor molecules. We could show that CD44v6 CAR-NK cells demonstrated effective cytotoxicity against TNBC in 3D spheroid models. The IL-15 superagonist was specifically released upon recognition of CD44v6 on TNBC and contributed to the cytotoxic attack. PD1 ligands are upregulated in TNBC and contribute to the immunosuppressive tumor microenvironment (TME). Competitive inhibition of PD1 neutralized inhibition by PD1 ligands expressed on TNBC. In total, CD44v6 CAR-NK cells are resistant to TME immunosuppression and offer a new therapeutic option for the treatment of BC, including TNBC.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
immunotherapy
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
9038
dcterms.bibliographicCitation.doi
10.3390/ijms24109038
dcterms.bibliographicCitation.journaltitle
International Journal of Molecular Sciences
dcterms.bibliographicCitation.number
10
dcterms.bibliographicCitation.originalpublishername
MDPI AG
dcterms.bibliographicCitation.volume
24
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37240385
dcterms.isPartOf.eissn
1422-0067