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1.
公开(公告)号:US20080038256A1
公开(公告)日:2008-02-14
申请号:US11626055
申请日:2007-01-23
申请人: Junho CHUNG , Kisu Kim
发明人: Junho CHUNG , Kisu Kim
IPC分类号: A61K39/395 , A61P35/00 , C07H21/04 , C07K16/22 , C40B10/00
CPC分类号: C07K16/32 , A61K39/39558 , A61K2039/505 , C07K2317/24 , A61K2300/00
摘要: The inventive anti-HGF/SF humanized antibody prepared by displaying on the surface of a phage an anti-HGF/SF chimeric Fab library comprising a set of human antibody light chain variable region (VL) and human antibody heavy chain variable region (VH) which are grafted with heavy chain complementary determining regions (HCDRs) of an anti-HGF/SF antibody of an animal other than human, has the equal or greater binding affinity than that of the parent anti-HGF/SF antibody, the neutralizing activity inhibiting the binding of HGF/SF to its receptor, cMET, while having the reduced immunogenicity in human. Therefore, the inventive anti-HGF/SF humanized antibody can be used for preventing and treating diseases effectively, e.g., cancers, by the action of binding HGF/SF to cMET.
摘要翻译: 通过在噬菌体表面上显示包含一组人抗体轻链可变区(V L L L)和人的抗HGF / SF嵌合Fab文库制备的本发明抗HGF / SF人源化抗体 用除人以外的动物的抗HGF / SF抗体的重链互补决定区(HCDR)接枝的抗体重链可变区(V H H H S)具有相等或更大的结合亲和力 与抗原HGF / SF抗体相比,中和活性抑制HGF / SF与其受体cMET的结合,同时在人体中具有降低的免疫原性。 因此,通过将HGF / SF结合到cMET的作用,本发明的抗HGF / SF人源化抗体可用于有效地预防和治疗疾病,例如癌症。
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公开(公告)号:US20080226650A1
公开(公告)日:2008-09-18
申请号:US12048636
申请日:2008-03-14
申请人: Sunyoung PARK , Junho CHUNG , Dohoon LEE , Jae-Gahb PARK
发明人: Sunyoung PARK , Junho CHUNG , Dohoon LEE , Jae-Gahb PARK
IPC分类号: A61K39/395 , C07K16/44 , C07H21/00 , A61P25/30 , C12N5/00
CPC分类号: C07K16/16 , C07K16/44 , C07K2317/24 , C07K2317/55
摘要: The present application discloses monoclonal antibody against cotinine and nicotine.
摘要翻译: 本申请公开了针对可替宁和尼古丁的单克隆抗体。
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公开(公告)号:US20100172902A1
公开(公告)日:2010-07-08
申请号:US12635392
申请日:2009-12-10
申请人: Junho CHUNG , Eun Kyung RYU , Ji Eun LEE , Sukmook LEE
发明人: Junho CHUNG , Eun Kyung RYU , Ji Eun LEE , Sukmook LEE
CPC分类号: C07K16/2836 , A61K2039/505 , C07K2317/24 , C07K2317/55 , C07K2317/565 , C07K2319/30
摘要: A method for treating a VCAM-1 mediated disease comprising administering a therapeutically effective amount of a monoclonal antibody to a patient in need thereof. The monoclonal antibody specifically binds to both human and mouse vascular cell adhesion molecule-1 (VCAM-1). The monoclonal antibody comprises(a) a light chain CDR 1 region defined by SEQ ID NO:5, a light chain CDR 2 region defined by SEQ ID NO:6, and a light chain CDR 3 region defined by SEQ ID NO:7, and (b) a heavy chain CDR 1 region defined by SEQ ID NO:8, a heavy chain CDR 2 region defined by SEQ ID NO:.9 or 11, and a heavy chain CDR 3 region defined by SEQ ID NO:10 or 12.
摘要翻译: 一种治疗VCAM-1介导的疾病的方法,其包括向有需要的患者施用治疗有效量的单克隆抗体。 单克隆抗体特异性结合人和小鼠血管细胞粘附分子-1(VCAM-1)。 单克隆抗体包含(a)由SEQ ID NO:5定义的轻链CDR1区,由SEQ ID NO:6定义的轻链CDR2区和由SEQ ID NO:7限定的轻链CDR3区, 或(b)由SEQ ID NO:8定义的重链CDR1区域,由SEQ ID NO:.9或11定义的重链CDR2区域和由SEQ ID NO:10定义的重链CDR3区域 12。
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