CAR-NK Cells Targeting HER1 (EGFR) Show Efficient Anti-Tumor Activity against Head and Neck Squamous Cell Carcinoma (HNSCC)

Author:

Nowak Juliette1,Bentele Marco1,Kutle Ivana1,Zimmermann Katharina1,Lühmann Jonathan Lukas2ORCID,Steinemann Doris2,Kloess Stephan3,Koehl Ulrike345,Roßberg Willi6,Ahmed Amed6,Schaudien Dirk7,Neubert Lavinia89,Kamp Jan-Christopher910ORCID,Kuehnel Mark P.89,Warnecke Athanasia6ORCID,Schambach Axel111,Morgan Michael1

Affiliation:

1. Institute of Experimental Hematology, Hannover Medical School, 30625 Hannover, Germany

2. Department of Human Genetics, Hannover Medical School, 30625 Hannover, Germany

3. Institute for Cellular Therapeutics, Hannover Medical School, 30625 Hannover, Germany

4. Institute of Clinical Immunology, University Leipzig, 04103 Leipzig, Germany

5. Fraunhofer Institute for Cell Therapy and Immunology, IZI, 04103 Leipzig, Germany

6. Department of Otolaryngology, Head and Neck Surgery, Hannover Medical School, 30625 Hannover, Germany

7. Fraunhofer Institute for Toxicology and Experimental Medicine, ITEM, 30625 Hannover, Germany

8. Institute of Pathology, Hannover Medical School, 30625 Hannover, Germany

9. Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), German Center for Lung Research (DZL), 30625 Hannover, Germany

10. Department of Respiratory Medicine, Hannover Medical School, 30625 Hannover, Germany

11. Division of Hematology/Oncology, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA

Abstract

(1) Background: HNSCC is a highly heterogeneous and relapse-prone form of cancer. We aimed to expand the immunological tool kit against HNSCC by conducting a functional screen to generate chimeric antigen receptor (CAR)-NK-92 cells that target HER1/epidermal growth factor receptor (EGFR). (2) Methods: Selected CAR-NK-92 cell candidates were tested for enhanced reduction of target cells, CD107a expression and IFNγ secretion in different co-culture models. For representative HNSCC models, patient-derived primary HNSCC (pHNSCC) cell lines were generated by employing an EpCAM-sorting approach to eliminate the high percentage of non-malignant cells found. (3) Results: 2D and 3D spheroid co-culture experiments showed that anti-HER1 CAR-NK-92 cells effectively eliminated SCC cell lines and primary HNSCC (pHNSCC) cells. Co-culture of tumor models with anti-HER1 CAR-NK-92 cells led to enhanced degranulation and IFNγ secretion of NK-92 cells and apoptosis of target cells. Furthermore, remaining pHNSCC cells showed upregulated expression of putative cancer stem cell marker CD44v6. (4) Conclusions: These results highlight the promising potential of CAR-NK cell therapy in HNSCC and the likely necessity to target multiple tumor-associated antigens to reduce currently high relapse rates.

Funder

Deutsche Krebshilfe

MHH Library

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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