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IMMUNOTHERAPEUTIC AGENT COMBINED WITH CD37, AND ITS COMBINATION WITH BIFUNCTIONAL CHEMOTHERAPEUTIC AGENT

机译:与CD37结合的免疫治疗剂及其与功能性化学治疗剂的结合

摘要

FIELD: biotechnologies.;SUBSTANCE: invention proposes a molecule that is specifically combined with CD37 and that contains the following from N-end to C-end: (a) CD37-specific scFV containing the following from N-end to C-end: (i) humanized variable region of a heavy chain, which contains CDR1 GYNMN, CDR2 NIDPYYGGTTYNRKFKG and CDR3 SVGPFDS, (ii) linker having 5 to 30 aminoacids inclusive, and (iii) humanized variable region of an easy chain containing CDR1 RASENVYSYLA, CDR2 FAKTLAE and CDR3 QHHSDNPWT; (b) a link region; and (c) immunoglobulin regions CH2 and CH3. The following is described: The following is described: nucleic acid coding the above binding molecule; an expression vector containing the above nucleic acid; and a host cell for production of a binding molecule, which contains the above vector. The invention proposes use of the above binding molecule to obtain a medicinal agent to reduce the number of B-cells, treatment of a disease or an illness, which is related to abnormal activity of B-cells. Besides, the invention describes compositions containing effective number of the above binding molecule to reduce the number of B-cells, treatment of a disease or an illness related to abnormal activity of B-cells.;EFFECT: invention allows obtaining scFV molecule binding CD37, having orientation of variable regions VHVL, with high yield and efficiency in comparison to scFV molecule against CD37, which has orientation of variable regions VLVH.;31 cl, 17 dwg, 13 tbl, 12 ex
机译:技术领域:发明内容:本发明提出一种分子,其与CD37特异性结合,并且从N端到C端包含以下分子:(a)从N端到C端包含以下CD37特异性scFV: (i)重链的人源化可变区,其包含CDR1 GYNMN,CDR2 NIDPYYGGTTYNRKFKG和CDR3 SVGPFDS,(ii)具有5至30个氨基酸(含5至30个氨基酸)的接头,和(iii)易链化的人源化可变区,其包含CDR1 RASENVYSYLA,CDR2 FAKTLAE和CDR3 QHHSDNPWT; (b)连结区; (c)免疫球蛋白区域CH2和CH3。描述以下内容:描述以下内容:编码上述结合分子的核酸;含有上述核酸的表达载体;含有上述载体的用于产生结合分子的宿主细胞。本发明提出上述结合分子在获得减少B细胞数目,治疗疾病或疾病的药物中的用途,所述药物与B细胞的异常活性有关。此外,本发明描述了包含有效数量的上述结合分子以减少B细胞数量,治疗与B细胞异常活性有关的疾病或疾病的组合物。效果:本发明允许获得结合scFV分子的CD37,具有抗可变区VLVH取向的scFV分子,与具有可变区VLVH取向的scFV分子相比,具有较高的收率和效率。; 31 cl,17 dwg,13 tbl,12 ex

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