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    • 7. 发明申请
    • DIAGNOSTIC METHOD FOR THE DETECTION OF CELLS EX VIVO
    • 用于检测细胞的诊断方法
    • WO2011138462A1
    • 2011-11-10
    • PCT/EP2011/057400
    • 2011-05-09
    • F. HOFFMANN-LA ROCHE AGDOBOSZ, MichaelSCHEUER, Werner
    • DOBOSZ, MichaelSCHEUER, Werner
    • G01N33/574A61K39/395A61K49/16C07K16/18C07K16/28
    • G01N33/566A61K49/0032A61K49/0058A61K2039/505C07K16/2863C07K16/32C07K16/4291G01N33/57484G01N33/57492
    • The present invention relates in essence to a method for detecting a subset of cells with a binding domain which is specific for a target which characterizes said subset of cells, which method comprises detecting, ex vivo, said subset of cells, wherein said binding domain is to be administered to a subject which comprises or is assumed to comprise said subset of cells, prior to the removal of said subset of cells. The present invention also relates to the use of a binding domain as defined herein in a method defined herein. The use of a binding domain as defined herein for the preparation of a diagnostic composition to be used in a method defined herein is also envisaged. In another aspect, the present invention relates to the binding domain as defined herein to be used in a method defined herein. Kits comprising a binding domain as defined herein and means to administer said binding domain to a subject, and, optionally, means to detect said binding domain with a method defined herein, are also disclosed. In another aspect, the present invention relates to the use of a binding domain, preferably a therapeutically effective antibody like for example alemtuzumab, apolizumab, cetuximab, epratuzumab, galiximab, gemtuzumab, ipilimumab, labetuzumab, panitumumab, rituximab, trastuzumab, nimotuzumab, mapatumumab, matuzumab, rhMab ICR62, rhMab B-Ly1 and pertuzumab etc including combinations thereof, for the preparation of a pharmaceutical composition for the treatment of patients disposed to respond favorably to said binding domain as identified by a method defined herein.
    • 本发明实质上涉及一种用于检测细胞子集的方法,所述结合域具有针对表征所述细胞亚群的靶特异性的结合域,所述方法包括离体检测细胞的所述子集,其中所述结合域为 在除去所述细胞子集之前,将其施用于包含或假设包含细胞子集的受试者。 本发明还涉及如本文定义的方法中定义的结合结构域的用途。 还设想使用如本文所定义的结合结构域来制备用于本文定义的方法中的诊断组合物。 在另一方面,本发明涉及如本文所定义的用于本文定义的方法的结合结构域。 还公开了包含如本文所定义的结合结构域的试剂盒和将受试者施用所述结合结构域的手段,以及任选地使用本文定义的方法检测所述结合结构域的手段。 另一方面,本发明涉及结合结构域,优选治疗有效的抗体,例如阿仑单抗,阿朴替珠单抗,西妥昔单抗,依普珠单抗,加利昔单抗,吉妥单抗,伊曲单抗,拉替珠单抗,帕尼单抗,利妥昔单抗,曲妥珠单抗,尼妥珠单抗, matuzumab,rhMab ICR62,rhMab B-Ly1和pertuzumab等包括其组合,用于制备用于治疗患者的药物组合物,所述药物组合物用于通过本文定义的方法鉴定的所述结合结构域有利地响应。