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    Molecular cancer therapeutics. 2014 Apr 22. pii: 1535-7163.MCT-13-0288. doi: 10.1158/1535-7163.MCT-13-0288. pmc: PMC4174294. mid: EMS60298
    Generation of a canine anti-EGFR (ErbB-1) antibody for passive immunotherapy in dog cancer patients.
    Singer J1,  Fazekas J2,  Wang W3,  Weichselbaumer M4,  Matz M5,  Mader A6,  Steinfellner W7,  Meitz S8,  Mechtcheriakova D9,  Sobanov Y10,  Willmann M11,  Stockner T12,  Spillner E13,  Kunert R14,  Jensen-Jarolim E15
    Author information
    1Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna; Comparative Medicine, Messerli Research Institute, University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna;
    2Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna; Comparative Medicine, Messerli Research Institute, University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna; Department for Applied Life Sciences, University of Applied Sciences, FH Campus Wien;
    3Department of Immunology, Capital Medical University, Beijing, PR China; and.
    4Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna; Comparative Medicine, Messerli Research Institute, University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna;
    5Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna;
    6Department of Biotechnology, VIBT-BOKU, University of Natural Resources and Life Sciences, Vienna, Austria;
    7Department of Biotechnology, VIBT-BOKU, University of Natural Resources and Life Sciences, Vienna, Austria;
    8Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna; Comparative Medicine, Messerli Research Institute, University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna;
    9Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna;
    10Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna;
    11Department for Companion Animals and Horses, University of Veterinary Medicine Vienna;
    12Centre for Physiology and Pharmacology, Medical University of Vienna;
    13Institute of Biochemistry and Molecular Biology, University of Hamburg, Hamburg, Germany.
    14Department of Biotechnology, VIBT-BOKU, University of Natural Resources and Life Sciences, Vienna, Austria;
    15Authors' Affiliations: Comparative Immunology and Oncology, Institute of Pathophysiology and Allergy Research, Medical University of Vienna; Comparative Medicine, Messerli Research Institute, University of Veterinary Medicine Vienna, Medical University Vienna and University Vienna; erika.jensen-jarolim@meduniwien.ac.at.
    Abstract

    Passive immunotherapy with monoclonal antibodies represents a cornerstone of human anticancer therapies, but has not been established in veterinary medicine yet. As the tumor-associated antigen EGFR (ErbB-1) is highly conserved between humans and dogs, and considering the effectiveness of the anti-EGFR antibody cetuximab in human clinical oncology, we present here a "caninized" version of this antibody, can225IgG, for comparative oncology studies. Variable region genes of 225, the murine precursor of cetuximab, were fused with canine constant heavy gamma and kappa chain genes, respectively, and transfected into Chinese hamster ovary (CHO) DUKX-B11 cells. Of note, 480 clones were screened and the best clones were selected according to productivity and highest specificity in EGFR-coated ELISA. Upon purification with Protein G, the recombinant cetuximab-like canine IgG was tested for integrity, correct assembly, and functionality. Specific binding to the surface of EGFR-overexpressing cells was assessed by flow cytometry and immunofluorescence; moreover, binding to canine mammary tissue was demonstrated by immunohistochemistry. In cell viability and proliferation assays, incubation with can225IgG led to significant tumor cell growth inhibition. Moreover, this antibody mediated significant tumor cell killing via phagocytosis in vitro. We thus present here, for the first time, the generation of a canine IgG antibody and its hypothetical structure. On the basis of its cetuximab-like binding site, on the one hand, and the expression of a 91% homologous EGFR molecule in canine cancer, on the other hand, this antibody may be a promising research compound to establish passive immunotherapy in dog patients with cancer.


    ©2014 American Association for Cancer Research.

    Publikations ID: 24755200
    Quelle: öffnen
     
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