Science and Research

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

(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.

  • Nowak, J.
  • Bentele, M.
  • Kutle, I.
  • Zimmermann, K.
  • Lühmann, J. L.
  • Steinemann, D.
  • Kloess, S.
  • Koehl, U.
  • Roßberg, W.
  • Ahmed, A.
  • Schaudien, D.
  • Neubert, L.
  • Kamp, J. C.
  • Kuehnel, M. P.
  • Warnecke, A.
  • Schambach, A.
  • Morgan, M.

Keywords

  • CAR-NK cells
  • CD44v6
  • Egfr
  • EpCAM
  • Her1
  • Hnscc
  • NK-92 cells
  • chimeric antigen receptor
  • head and neck cancer
  • immunotherapy
Publication details
DOI: 10.3390/cancers15123169
Journal: Cancers (Basel)
Number: 12
Work Type: Original
Location: BREATH
Disease Area: LC
Partner / Member: MHH
Access-Number: 37370779

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