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Human kappa light chain targeted Pseudomonas exotoxin A - identifying human antibodies and Fab fragments with favorable characteristics for antibody-drug conjugate development

C. Kellner, W. K. Bleeker, J. J. Lammerts van Bueren, M. Staudinger, K. Klausz, S. Derer, P. Glorius, A. Muskulus, B. E.C.G. de Goeij, J. G.J. van de Winkel, P. W.H.I. Parren, T. Valerius, M. Gramatzki, M. Peipp*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Antibody-drug conjugates (ADC) represent promising agents for targeted cancer therapy. To allow rational selection of human antibodies with favorable characteristics for ADC development a screening tool was designed obviating the need of preparing individual covalently linked conjugates. Therefore, α-kappa-ETA' was designed as a fusion protein consisting of a human kappa light chain binding antibody fragment and a truncated version of Pseudomonas exotoxin A α-kappa-ETA' specifically bound to human kappa light chains of human or human-mouse chimeric antibodies and Fab fragments. Antibody-redirected α-kappa-ETA' specifically inhibited proliferation of antigen-expressing cell lines at low toxin and antibody concentrations. Selected antibodies that efficiently delivered α-kappa-ETA' in the novel assay system were used to generate scFv-based covalently linked immunotoxins. These molecules efficiently triggered apoptosis of target cells, indicating that antibodies identified in our assay system can be converted to functional immunoconjugates. Finally, a panel of human epidermal growth factor receptor (EGFR) antibodies was screened - demonstrating favorable characteristics with antibody 2F8. These data suggest that antibodies with potential for Pseudomonas exotoxin A-based ADC development can be identified using the novel α-kappa-ETA' conjugate.

OriginalspracheEnglisch
ZeitschriftJournal of Immunological Methods
Jahrgang371
Ausgabenummer1-2
Seiten (von - bis)122-133
Seitenumfang12
ISSN0022-1759
DOIs
PublikationsstatusVeröffentlicht - 31.08.2011

Fördermittel

Heidi Bosse, Britta von Below and Daniela Hallack are acknowledged for expert technical assistance. This study was supported by research grant 2007.065.1 from the Wilhelm Sander-Stiftung , research grant DJCLS R 08/01 from the Deutsche José Carreras Leukaemie Stiftung e.V. ; research grant VA124/7-1 from the Deutsche Forschungs Gemeinschaft (DFG) ; research grant from the Werner und Klara Kreitz-Stiftung and intramural funding from the Christian-Albrechts-University Kiel .

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

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