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2D7 diabody bound to the alpha2 domain of HLA class I efficiently induces caspase-independent cell death against malignant and activated lymphoid cells
Authors:Kimura Naoki  Kawai Shigeto  Kinoshita Yasuko  Ishiguro Takahiro  Azuma Yumiko  Ozaki Shuji  Abe Masahiro  Sugimoto Masamichi  Hirata Yuichi  Orita Tetsuro  Okabe Hisafumi  Matsumoto Toshio  Tsuchiya Masayuki
Affiliation:Genome Antibody Product Research Department, Chugai Pharmaceutical Co., Ltd., Japan. kimuranok@chugai-pharm.co.jp
Abstract:
A mouse monoclonal antibody (2D7 mAb), which specifically bound to the alpha2 domain of HLA class I, rapidly induces cell aggregation accompanied by weak cytotoxicity against ARH-77 cells, suggesting that 2D7 mAb had a potential for agonist antibody. In order to enhance this cytotoxicity, 2D7 mAb was engineered to be a small bivalent antibody fragment, 2D7 diabody. The resultant 2D7 diabody showed a strong cytotoxicity against ARH-77 cells. As a notable characteristic feature, the lethal effect of 2D7 diabody was quite rapid, mediated by a caspase-independent death pathway. Furthermore, 2D7 diabody also showed cytotoxicity against several leukemia and lymphoma cell lines, and mitogen-activated peripheral blood mononuclear cells (PBMC), but not for normal resting PBMC and adherent cell lines such as HUVEC. These results suggest that 2D7 diabody could be expected as a novel therapeutic antibody for hematological malignancies as well as inflammatory diseases.
Keywords:Agonist antibody   Diabody   HLA class I   Cell death   Therapeutic antibody   Hematological malignancy
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