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USE OF ANTIBODY AGAINST CD20 TYPE II WITH INCREASED ANTIBODY-DEPENDENT CELL-MEDIATED CYTOTOXICITY (ADCC) IN COMBINATION WITH CYCLOPHOSPHAMIDE, VINCRISTINE, AND DOXORUBICIN FOR TREATMENT OF NON-HODGKIN LYMPHOMA
USE OF ANTIBODY AGAINST CD20 TYPE II WITH INCREASED ANTIBODY-DEPENDENT CELL-MEDIATED CYTOTOXICITY (ADCC) IN COMBINATION WITH CYCLOPHOSPHAMIDE, VINCRISTINE, AND DOXORUBICIN FOR TREATMENT OF NON-HODGKIN LYMPHOMA
The invention relates to the use of the humanized B-Lyl (B-HH6-B-KV1 GE) antibody with the variable region of the heavy chain (VH) represented in SEQ ID NO: 7 and the variable region of the light chain represented in SEQ ID NO: the humanized B-Lyl antibody constructed using glycoengineering techniques, at least 40 % of oligosaccharides in Fc-region are non-fucosilated. The said antibody is proposed as the component for preparing anticancer agent wherein CD20 is expressed in combination with at least one chemotherapeutic agent selected from the group comprising Cyclophosphamide, Vincristine, and Doxorubicin. The treatment with anti-CD20 type II is provided in combination with a) Cyclophosphamide and Vincristine, b) Doxorubicin, c) Cyclophosphamide, d) Cyclophosphamide, Vincristine, and Doxorubicin.
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机译:本发明涉及人源化B-Lyl(B-HH6-B-KV1 GE)抗体与SEQ ID NO:7所示的重链(VH)的可变区和轻链的可变区的用途。在SEQ ID NO:使用糖工程技术构建的人源化B-Lyl抗体中,Fc区中至少40%的寡糖是非岩藻糖基化的。提出将所述抗体用作制备抗癌剂的成分,其中CD20与选自环磷酰胺,长春新碱和阿霉素的至少一种化学治疗剂组合表达。 II型抗CD20治疗与a)环磷酰胺和长春新碱,b)阿霉素,c)环磷酰胺,d)环磷酰胺,长春新碱和阿霉素组合提供。
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