Abstract:
The present invention relates to anti-Axl antibodies and uses thereof in diagnostic and therapeutic methods. More particularly, the present invention relates to a monoclonal antibody having specificity for Axl comprising an heavy chain variable region comprising SEQ ID NO:2 in the H-CDR1 region, SEQ ID NO:3 in the H-CDR2 region and SEQ ID NO:4 in the H-CDR3 region; and a light chain variable region comprising SEQ ID NO: 6 in the L-CDR1 region, SEQ ID NO:7 in the L-CDR2 region and SEQ ID NO:8 in the L-CDR3 region. Said monoclonal antibody binds to the extracellular domain of Axl via, SEQ ID NO:9, SEQ ID NO: 10 and SEQ ID NO: 11.
Abstract translation:本发明涉及抗Ax1抗体及其在诊断和治疗方法中的用途。 更具体地说,本发明涉及对Ax1具有特异性的单克隆抗体,其包含H-CDR1区中包含SEQ ID NO:2的重链可变区,H-CDR2区中的SEQ ID NO:3和SEQ ID NO: 4在H-CDR3区域; 以及包含L-CDR1区中的SEQ ID NO:6,L-CDR2区的SEQ ID NO:7和L-CDR3区的SEQ ID NO:8的轻链可变区。 所述单克隆抗体通过SEQ ID NO:9,SEQ ID NO:10和SEQ ID NO:11结合Ax1的细胞外结构域。
Abstract:
The present invention relates to anti-Axl antibodies and uses thereof in diagnostic and therapeutic methods. More particularly, the present invention relates to a monoclonal antibody having specificity for Axl comprising an heavy chain variable region comprising SEQ ID NO:2 in the H-CDR1 region, SEQ ID NO:3 in the H-CDR2 region and SEQ ID NO:4 in the H-CDR3 region; and a light chain variable region comprising SEQ ID NO: 6 in the L-CDR1 region, SEQ ID NO:7 in the L-CDR2 region and SEQ ID NO:8 in the L-CDR3 region. Said monoclonal antibody binds to the extracellular domain of Axl via, SEQ ID NO:9 and SEQ ID NO: 10.
Abstract translation:本发明涉及抗Ax1抗体及其在诊断和治疗方法中的用途。 更具体地说,本发明涉及对Ax1具有特异性的单克隆抗体,其包含H-CDR1区中包含SEQ ID NO:2的重链可变区,H-CDR2区中的SEQ ID NO:3和SEQ ID NO: 4在H-CDR3区域; 以及包含L-CDR1区中的SEQ ID NO:6,L-CDR2区的SEQ ID NO:7和L-CDR3区的SEQ ID NO:8的轻链可变区。 所述单克隆抗体通过SEQ ID NO:9和SEQ ID NO:10与Ax1的细胞外结构域结合。
Abstract:
The present invention relates to a method of treating a subject having a cancer in a body cavity characterized in that it comprises the steps of: administering in said body cavity of the subject radiolabeled binding molecules which bind to an antigen expressed by cancerous cells; washing the body cavity to remove unbound radiolabeled molecules. The present invention also relates to a body cavity perfusing system for carrying out said method.
Abstract:
The present invention provides recombinant CEA glycoproteins and methods for their production. These recombinant CEA glycoproteins s lack the C-terminal 26 amino acids which are present in natural CEA and are characterized in that they are free from cross-reactive CEA-like antigens, antigenically indistingiushable from the soluble form of CEA shed from tumor cells, and devoid of the ethanolamine which is present at the C-terminus of natural CEA, and also devoid of the additional amino acids which may be attached to the natural CEA through said ethanolamine. Said recombinant CEA glycoproteins s preferably have the amino acid sequence SEQ ID NO: 1. The CEA glycoproteins s of the invention may be used as reagents in an immunoassay for the diagnosis of neoplastic diseases. The invention also relates to a DNA encoding said recombinant CEA glycoprotein, such as the DNA having the nucleotide sequence SEQ ID NO: 2 or a functional equivalent sequence thereof. The present invention also relates to recombinant vectors comprising said DNA, which recombinant vector is capable of directing the expression of said DNA in a compatible host cell, and to transformed host cells containing such a recombinant vector. The recombinant CEA glycoprotein of the present invention, preferably integrated in a test-kit, may be used for determining the presence of tumor cells in a sample of body fluid.
Abstract translation:本发明提供重组CEA糖蛋白及其生产方法。 这些重组CEA糖蛋白缺乏存在于天然CEA中的C-末端26个氨基酸,其特征在于它们不具有从可溶形式从肿瘤细胞中流出的CEA抗原性不可抵抗的交叉反应性CEA-样抗原,以及 没有存在于天然CEA的C末端的乙醇胺,也没有可以通过所述乙醇胺与天然CEA连接的另外的氨基酸。 所述重组CEA糖蛋白优选具有SEQ ID NO:1的氨基酸序列。本发明的CEA糖蛋白可用作用于诊断肿瘤疾病的免疫测定中的试剂。 本发明还涉及编码所述重组CEA糖蛋白的DNA,例如具有核苷酸序列SEQ ID NO:2的DNA或其功能等同序列。 本发明还涉及包含所述DNA的重组载体,所述重组载体能够引导所述DNA在相容宿主细胞中的表达,以及含有这种重组载体的转化宿主细胞。 优选整合在试验盒中的本发明的重组CEA糖蛋白可用于测定体液样品中肿瘤细胞的存在。
Abstract:
The present invention relates to anti-Axl antibodies and uses thereof in diagnostic and therapeutic methods. More particularly, the present invention relates to a monoclonal antibody having specificity for Axl comprising an heavy chain variable region comprising SEQ ID NO:2 in the H-CDR1 region, SEQ ID NO:3 in the H-CDR2 region and SEQ ID NO:4 in the H-CDR3 region; and a light chain variable region comprising SEQ ID NO: 6 in the L-CDR1 region, SEQ ID NO:7 in the L-CDR2 region and SEQ ID NO:8 in the L-CDR3 region. Said monoclonal antibody binds to the extracellular domain of Axl via, SEQ ID NO:9, SEQ ID NO: 10 and SEQ ID NO: 11.
Abstract translation:本发明涉及抗Ax1抗体及其在诊断和治疗方法中的用途。 更具体地说,本发明涉及对Ax1具有特异性的单克隆抗体,其包含H-CDR1区中包含SEQ ID NO:2的重链可变区,H-CDR2区中的SEQ ID NO:3和SEQ ID NO: 4在H-CDR3区域; 以及包含L-CDR1区中的SEQ ID NO:6,L-CDR2区的SEQ ID NO:7和L-CDR3区的SEQ ID NO:8的轻链可变区。 所述单克隆抗体通过SEQ ID NO:9,SEQ ID NO:10和SEQ ID NO:11结合Ax1的细胞外结构域。
Abstract:
The present invention provides for isolated anti-human-HER3 antibodies or fragments thereof. More particularly the present invention provides an isolated monoclonal antibody that specifically binds to the extracellular domain of HER-3 and competes for binding to the extracellular domain of human HER-3 with the antibody produced obtainable from hybridoma deposited as CNCM-I-4486. The antibodies described in the present invention are useful for the treatment of cancer.
Abstract:
The present invention provides for isolated anti-human-HER3 antibodies or fragments thereof. More particularly the present invention provides an isolated monoclonal antibody that specifically binds to the extracellular domain of HER-3 and competes for binding to the extracellular domain of human HER-3 with the antibody produced obtainable from hybridoma deposited as CNCM-I-4486. The antibodies described in the present invention are useful for the treatment of cancer.
Abstract:
The invention concerns an in-vitro method for introducing a targeted genome modification into an oocyte or an egg and a method for performing a random insertion in the genome of a host cell.
Abstract:
This invention relates to human anti-idiotypic antibody fragments, especially scFv, characterized by the ability to mimic Her-2/neu tumor associated antigen. These antibody fragments are promising candidates for active immunotherapy for cancer patients positive for Her-2/neu.