Targeting EpCAM by a Bispecific Trifunctional Antibody Exerts Profound Cytotoxic Efficacy in Germ Cell Tumor Cell Lines
Autor: | Anna Casati, Gabriele Calaminus, Daniel Nettersheim, Dagmar Dilloo, Mahsa Mohseni, Rogerio B. Craveiro, Hubert Schorle, Stefan Schönberger, Daniela Kraft |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
embryonal carcinoma Cancer Research T cell medicine.medical_treatment Catumaxomab Medizin lcsh:RC254-282 Article Embryonal carcinoma 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine medicine choriocarcinoma Cytotoxic T cell germ cell tumors biology seminoma Epithelial cell adhesion molecule Immunotherapy medicine.disease lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens Trifunctional antibody CD3 bispecific antibody 030104 developmental biology medicine.anatomical_structure Oncology chemistry 030220 oncology & carcinogenesis EpCAM biology.protein Cancer research immunotherapy Antibody medicine.drug |
Zdroj: | Cancers Cancers, Vol 12, Iss 1279, p 1279 (2020) Volume 12 Issue 5 |
ISSN: | 2072-6694 |
Popis: | Outcome in high-risk patients with refractory or relapsed germ cell tumours (GCT) remains poor. Novel strategies enhancing therapeutic efficacy whilst limiting therapeutic burden are warranted, yet immunotherapy approaches geared towards activating endogenous antitumor responses have not been successful thus far. Redirection of cytotoxic effector cells by bispecific antibodies represents a promising approach in this setting. We demonstrate that the Epithelial Cell Adhesion Molecule (EpCAM) is broadly expressed in GCT cell lines of different histologic origin including seminoma, choriocarcinoma (CHC), and embryonal carcinoma (EC). In these GCT lines of variable EpCAM surface expression, targeting T cells by the prototypic bispecific EpCAM/CD3-antibody (bAb) Catumaxomab together with natural killer (NK) cell engagement via the Fc domain promotes profound cytotoxicity across a broad range of antibody dilutions. In contrast, tumor cell lysis mediated by either immune cell subset alone is influenced by surface density of the target antigen. In the CHC line JAR, NK cell-dependent cytotoxicity dominates, which may be attributed to differential surface expression of immunomodulatory proteins such as MHC-I, CD24, and Fas receptors on CHC and EC. In view of redirecting T cell therapy mediated by bispecific antibodies, such differences in GCT immunophenotype potentially favoring immune escape are worth further investigation. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |