Precision Immunotherapy Utilizing Adapter CAR-T Cells (AdCAR-T) in Metastatic Breast Cancer Leads to Target Specific Lysis

Author:

Önder Cansu E.1ORCID,Moustafa-Oglou Moustafa2,Schröder Sarah M.34ORCID,Hartkopf Andreas D.5ORCID,Koch André15ORCID,Seitz Christian M.267ORCID

Affiliation:

1. Research Institute for Women’s Health, University of Tübingen, 72076 Tübingen, Germany

2. Department of Pediatric Oncology and Hematology, University Hospital Tübingen, 72076 Tübingen, Germany

3. Department of Otorhinolaryngology, Head and Neck Surgery, University of Ulm, 89081 Ulm, Germany

4. Department of Peptide-Based Immunotherapy, University and University Hospital Tübingen, 72076 Tübingen, Germany

5. Department of Women’s Health, University of Tübingen, 72076 Tübingen, Germany

6. Cluster of Excellence iFIT (EXC 2180) “Image-Guided and Functionally Instructed Tumor Therapies”, University of Tübingen, 72076 Tübingen, Germany

7. German Cancer Consortium (DKTK), Partner Site Tübingen, a Partnership between German Cancer Research Center (DKFZ) and University Hospital Tübingen, 81675 Munich, Germany

Abstract

A frequent symptom of metastasized breast cancer (BC) includes the development of malignant pleural effusion (MPE), which contains malignant cells derived from the primary tumor site. The poor prognosis of MPE in metastasized BC indicates the necessity for dependable precision oncology and the importance of models representing the heterogenous nature of metastatic BC. In this study, we cultured MPE-derived metastatic tumor cells from four advanced BC patients using organoid technology. We assessed the expression of tumor-associated antigens on MPE-derived organoid lines by flow cytometry (FC). Based on an individual antigen expression pattern, patient-derived organoids were treated with adapter CAR-T cells (AdCAR-T) and biotinylated monoclonal antibodies targeting CD276, HER2, EGFR, TROP2, or EpCAM. Co-culture assays revealed specific organoid lysis by AdCAR-T depending on individual antigen expression patterns. Our results demonstrate that MPE-derived organoids can serve as a reliable tool for assessing the efficacy of AdCAR-T on metastatic BC in a patient-individualized manner. This approach could potentially be applied in a preclinical setting to instruct therapy decisions. Further, our study demonstrates the feasibility of precision immunotherapy utilizing AdCAR-T to target patient-individualized antigen patterns.

Funder

German Cancer Aid

Open Access Publication Fund of the University of Tübingen

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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