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Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer
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 m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218876/ https://www.ncbi.nlm.nih.gov/pubmed/37240385 http://dx.doi.org/10.3390/ijms24109038 |
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author | Raftery, Martin J. Franzén, Alexander Sebastian Radecke, Clarissa Boulifa, Abdelhadi Schönrich, Günther Stintzing, Sebastian Blohmer, Jens-Uwe Pecher, Gabriele |
author_facet | Raftery, Martin J. Franzén, Alexander Sebastian Radecke, Clarissa Boulifa, Abdelhadi Schönrich, Günther Stintzing, Sebastian Blohmer, Jens-Uwe Pecher, Gabriele |
author_sort | Raftery, Martin J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10218876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102188762023-05-27 Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer Raftery, Martin J. Franzén, Alexander Sebastian Radecke, Clarissa Boulifa, Abdelhadi Schönrich, Günther Stintzing, Sebastian Blohmer, Jens-Uwe Pecher, Gabriele Int J Mol Sci Article 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. MDPI 2023-05-20 /pmc/articles/PMC10218876/ /pubmed/37240385 http://dx.doi.org/10.3390/ijms24109038 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Raftery, Martin J. Franzén, Alexander Sebastian Radecke, Clarissa Boulifa, Abdelhadi Schönrich, Günther Stintzing, Sebastian Blohmer, Jens-Uwe Pecher, Gabriele Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title | Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title_full | Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title_fullStr | Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title_full_unstemmed | Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title_short | Next Generation CD44v6-Specific CAR-NK Cells Effective against Triple Negative Breast Cancer |
title_sort | next generation cd44v6-specific car-nk cells effective against triple negative breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218876/ https://www.ncbi.nlm.nih.gov/pubmed/37240385 http://dx.doi.org/10.3390/ijms24109038 |
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