TY - JOUR
T1 - Human kappa light chain targeted Pseudomonas exotoxin A - identifying human antibodies and Fab fragments with favorable characteristics for antibody-drug conjugate development
AU - Kellner, C.
AU - Bleeker, W. K.
AU - Lammerts van Bueren, J. J.
AU - Staudinger, M.
AU - Klausz, K.
AU - Derer, S.
AU - Glorius, P.
AU - Muskulus, A.
AU - de Goeij, B. E.C.G.
AU - van de Winkel, J. G.J.
AU - Parren, P. W.H.I.
AU - Valerius, T.
AU - Gramatzki, M.
AU - Peipp, M.
N1 - Funding Information:
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 .
Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2011/8/31
Y1 - 2011/8/31
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=79960936401&partnerID=8YFLogxK
U2 - 10.1016/j.jim.2011.06.023
DO - 10.1016/j.jim.2011.06.023
M3 - Journal articles
C2 - 21756911
AN - SCOPUS:79960936401
SN - 0022-1759
VL - 371
SP - 122
EP - 133
JO - Journal of Immunological Methods
JF - Journal of Immunological Methods
IS - 1-2
ER -