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  1. No Access

    Reference Work Entry In depth

    Glyco-engineered Therapeutic Antibodies as a Second-Generation Antibody Therapy

    Since the establishment of monoclonal antibody production using mouse hybridoma technology in the 1980s, there has been expanding progress and continuous technological improvement in the development of therape...

    Rinpei Niwa, Kenya Shitara, Mitsuo Satoh in Glycoscience: Biology and Medicine (2015)

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    Living Reference Work Entry In depth

    Glyco-engineered Therapeutic Antibodies as a Second-Generation Antibody Therapy

    Since the establishment of monoclonal antibody production using mouse hybridoma technology in the 1980s, there has been expanding progress and continuous technological improvement in the development of therape...

    Rinpei Niwa Ph.D., Kenya Shitara, Mitsuo Satoh in Glycoscience: Biology and Medicine

  3. Article

    Open Access

    Two mechanisms of the enhanced antibody-dependent cellular cytotoxicity (ADCC) efficacy of non-fucosylated therapeutic antibodies in human blood

    Antibody-dependent cellular cytotoxicity (ADCC) has recently been identified as one of the critical mechanisms underlying the clinical efficacy of therapeutic antibodies, especially anticancer antibodies. Ther...

    Shigeru Iida, Reiko Kuni-Kamochi, Katsuhiro Mori, Hirofumi Misaka, Miho Inoue in BMC Cancer (2009)

  4. No Access

    Chapter and Conference Paper

    Non-fucosylated Therapeutic Antibodies: The Next Generation of Therapeutic Antibodies

    Therapeutic antibody IgG1 has two N-linked oligosaccharide chains bound to the Fc region. The oligosaccharides are of the complex biantennary type, composed of a trimannosyl core structure with the presence or ab...

    Mitsuo Satoh, Shigeru Iida in Animal Cell Technology: Basic & Applied As… (2009)

  5. No Access

    Article

    Non-fucosylated therapeutic antibodies: the next generation of therapeutic antibodies

    Therapeutic antibody IgG1 has two N-linked oligosaccharide chains bound to the Fc region. The oligosaccharides are of the complex biantennary type, composed of a trimannosyl core structure with the presence or...

    Katsuhiro Mori, Shigeru Iida, Naoko Yamane-Ohnuki, Yutaka Kanda in Cytotechnology (2007)

  6. Article

    Open Access

    Double knockdown of α1,6-fucosyltransferase (FUT8) and GDP-mannose 4,6-dehydratase (GMD) in antibody-producing cells: a new strategy for generating fully non-fucosylated therapeutic antibodies with enhanced ADCC

    Antibody-dependent cellular cytotoxicity (ADCC) is greatly enhanced by the absence of the core fucose of oligosaccharides attached to the Fc, and is closely related to the clinical efficacy of anticancer activ...

    Harue Imai-Nishiya, Katsuhiro Mori, Miho Inoue, Masako Wakitani in BMC Biotechnology (2007)

  7. No Access

    Chapter and Conference Paper

    Thermodynamic and kinetic effects of human IgG1 defucosylation on IgG1-FcγRIIIa interaction

    Akira Okazaki, Emi Shoji, Kazuyasu Nakamura in Animal Cell Technology: Basic & Applied As… (2006)

  8. No Access

    Chapter and Conference Paper

    Generation of an industrially ideal host cell line for producing completely-defucosylated antibody with enhanced antibody-dependent cellular cytotoxicity (ADCC)

    Mitsuo Satoh, Naoko Yamane-Ohnuki in Animal Cell Technology: Basic & Applied As… (2006)

  9. No Access

    Article

    Construction of humanized anti-ganglioside monoclonal antibodies with potent immune effector functions

     Gangliosides GD3, GD2 and GM2, which are the major gangliosides expressed on most human cancers of neuroectodermal and epithelial origin, have been focused on as effective targets for passive immunotherapy wi...

    Kazuyasu Nakamura, Yuko Tanaka, Kenya Shitara in Cancer Immunology, Immunotherapy (2001)

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    Article

    Recombinant antibodies against ganglioside expressed on tumor cells

    Several gangliosides such as GM2, GD2, and GD3 have been thought of as target molecules for active or passive immunotherapy of human cancers because of their dominant expression on the tumor cell surface, esp...

    Nobuo Hanai, Kazuyasu Nakamura, Kenya Shitara in Cancer Chemotherapy and Pharmacology (2000)

  11. No Access

    Article

    Therapeutic potential of chimeric anti-(ganglioside GD3) antibody KM871: antitumor activity in xenograft model of melanoma and effector function analysis

    KM871 is a chimeric antibody recognizing ganglioside GD3, which is one of the major gangliosides expressed on the cell surface of human tumors of neuroectodermal origin. This study demonstrates the antitumor ...

    Junji Kanazawa, So Ohta, Kenya Shitara, Fumiko Fujita in Cancer Immunology, Immunotherapy (2000)

  12. No Access

    Article

    Roles of two VEGF receptors, Flt-1 and KDR, in the signal transduction of VEGF effects in human vascular endothelial cells

    Vascular endothelial growth factor (VEGF) is a principal regulator of vasculogenesis and angiogenesis. VEGF expresses its effects by binding to two VEGF receptors, Flt-1 and KDR. However, properties of Flt-1 a...

    Shinichi Kanno, Nobuyuki Oda, Mayumi Abe, Yoshito Terai, Mikito Ito in Oncogene (2000)

  13. No Access

    Article

    Panosialins, inhibitors of an α1,3-fucosyltransferase Fuc-TVII, suppress the expression of selectin ligands on U937 cells

    Panosialins A and B were isolated as inhibitors of an α1,3-fucosyltransferase, Fuc-TVII, which is a key enzyme in the biosynthesis of selectin ligands, from culture broth of Streptomyces sp. Panosialins A and ...

    Katsumi Shinoda, Kenya Shitara, Yuko Yoshihara, Akira Kusano in Glycoconjugate Journal (1998)

  14. No Access

    Article

    A mouse/human chimeric anti-(ganglioside GD3) antibody with enhanced antitumor activities

    Ganglioside GD3, which is one of the major gangliosides expressed on the cell surface of human tumors of neuroectodermal origin has been focused on as a target molecule for passive immunotherapy. We have clone...

    Kenya Shitara, Yoshihisa Kuwana, Kazuyasu Nakamura in Cancer Immunology, Immunotherapy (1993)