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公开(公告)号:US09422366B2
公开(公告)日:2016-08-23
申请号:US14134779
申请日:2013-12-19
发明人: Leonardo Borras , Tea Gunde , David Urech
IPC分类号: C07K16/24
CPC分类号: C07K16/241 , C07K2317/24 , C07K2317/55 , C07K2317/565 , C07K2317/567 , C07K2317/622 , C07K2317/92
摘要: The present invention relates to particularly stable and soluble scFv antibodies and Fab fragments specific for TNF, which comprise specific light chain and heavy chain sequences that are optimized for stability, solubility, in vitro and in vivo binding of TNF, and low immunogenicity. Said antibodies are designed for the diagnosis and/or treatment of TNF-mediated disorders. The nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.
摘要翻译: 本发明涉及特别稳定和可溶的scFv抗体和对TNF特异性的Fab片段,其包含针对TNF的稳定性,溶解性,体外和体内结合以及低免疫原性而优化的特异性轻链和重链序列。 所述抗体被设计用于诊断和/或治疗TNF介导的病症。 还公开了用于表达本发明的重组抗体的核酸,载体和宿主细胞,用于分离它们的方法和所述抗体在医学中的用途。
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公开(公告)号:US20140171634A1
公开(公告)日:2014-06-19
申请号:US14185783
申请日:2014-02-20
IPC分类号: C07K16/24
CPC分类号: C07K16/241 , A61K2039/505 , C07K2317/14 , C07K2317/21 , C07K2317/24 , C07K2317/522 , C07K2317/55 , C07K2317/56 , C07K2317/565 , C07K2317/567 , C07K2317/622 , C07K2317/76 , C07K2317/92 , C07K2317/94
摘要: The present invention relates to particularly stable and soluble scFv antibodies and Fab fragments specific for TNFα, which comprise specific light chain and heavy chain sequences that are optimized for stability, solubility, in vitro and in vivo binding of TNFα, and low immunogenicity. Said antibodies are designed for the diagnosis and/or treatment of TNFα-related disorders. The nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.
摘要翻译: 本发明涉及特别稳定和可溶的scFv抗体和对TNFα特异性的Fab片段,其包含针对TNFα的稳定性,溶解性,体外和体内结合而优化的特异性轻链和重链序列以及低免疫原性。 所述抗体被设计用于诊断和/或治疗TNFα相关疾病。 还公开了用于表达本发明的重组抗体的核酸,载体和宿主细胞,用于分离它们的方法和所述抗体在医学中的用途。
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公开(公告)号:US08637022B2
公开(公告)日:2014-01-28
申请号:US13000499
申请日:2009-06-30
申请人: David Urech
发明人: David Urech
IPC分类号: A61K38/00
CPC分类号: C12N15/1062 , A61K47/48215 , A61K47/48338 , A61K47/60 , A61K47/65 , C07K16/00 , C07K16/241 , C07K2317/40 , C07K2317/41 , C07K2317/622 , C07K2319/31 , C12N15/1037
摘要: The invention provides functionalized polypeptides, especially therapeutic polypeptides (e.g., scFv), comprising a linker sequence that can be rapidly and specifically functionalized by the addition of one or functional moieties (e.g., PEG) or binding specificities (e.g., an amino acid sequence with a particular binding specificity). Such functionalized polypeptides are advantageous in that they have improved pharmacokinetic properties (e.g., improved in vivo half-life, tissue penetration and tissue residency time) over non-functionalized polypeptides. Methods for the rapid and reproducible generation of functionalized polypeptides are also provided.
摘要翻译: 本发明提供功能化多肽,特别是治疗性多肽(例如scFv),其包含可以通过加入一个或多个功能部分(例如PEG)或结合特异性(例如,具有 特异性结合特异性)。 这样的功能化多肽的优点在于它们具有比非功能化多肽更好的药代动力学性质(例如,改善的体内半衰期,组织穿透和组织停留时间)。 还提供了快速和可重复产生功能化多肽的方法。
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公开(公告)号:US08227199B2
公开(公告)日:2012-07-24
申请号:US12710579
申请日:2010-02-23
IPC分类号: G01N33/53 , G01N33/567 , G01N1/30 , G01N33/48
CPC分类号: C07K16/2866 , C07K16/22 , C07K16/241 , C07K16/28 , C07K16/4241 , C07K2317/20 , C07K2317/21 , C07K2317/24 , C07K2317/569 , C07K2317/622 , G01N33/5052 , G01N33/566 , G01N33/56972
摘要: The invention provides methods for identifying immunobinders, such as scFv antibodies, capable of specifically binding to cell surface antigens, and compositions identified according to said methods.
摘要翻译: 本发明提供用于鉴定能够特异性结合细胞表面抗原的免疫结合剂如scFv抗体以及根据所述方法鉴定的组合物的方法。
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公开(公告)号:US20120014958A1
公开(公告)日:2012-01-19
申请号:US13000423
申请日:2009-06-25
申请人: Leonardo Borras , David Urech , Tea Gunde
发明人: Leonardo Borras , David Urech , Tea Gunde
IPC分类号: A61K39/395 , C12N15/13 , C12N15/63 , C12N5/10 , C12N1/21 , C12N1/19 , C12N5/16 , C07K7/06 , C07K1/00 , A61P35/00 , A61P27/02 , A61P27/06 , A61P7/10 , A61P19/02 , A61P17/06 , A61P9/10 , C07K16/22
CPC分类号: C07K16/22 , C07K1/00 , C07K7/06 , C07K2317/24 , C07K2317/54 , C07K2317/55 , C07K2317/56 , C07K2317/565 , C07K2317/567 , C07K2317/622 , C07K2317/73 , C07K2317/92
摘要: The present invention relates to soluble and stable anti-VEGF immunobinders comprising CDRs from rabbit monoclonal antibodies. Said antibodies are designed for the diagnosis and/or treatment of VEGF-mediated disorders. The hybridomas, nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.
摘要翻译: 本发明涉及包含来自兔单克隆抗体的CDR的可溶性和稳定的抗-VEGF免疫结合剂。 所述抗体被设计用于诊断和/或治疗VEGF介导的病症。 还公开了用于表达本发明的重组抗体的杂交瘤,核酸,载体和宿主细胞,其分离方法和所述抗体在医学中的用途。
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公开(公告)号:US20110159007A1
公开(公告)日:2011-06-30
申请号:US13000345
申请日:2009-06-25
申请人: Leonardo Borras , Tea Gunde , David Urech
发明人: Leonardo Borras , Tea Gunde , David Urech
IPC分类号: A61K39/395 , C07K16/24 , C12N15/13 , C12N15/63 , C12N5/00 , A61P37/06 , A61P29/00 , A61P25/00 , A61P1/00 , A61P17/06 , A61P19/02 , A61P13/12 , A61P9/00
CPC分类号: C07K16/241 , C07K2317/24 , C07K2317/55 , C07K2317/565 , C07K2317/567 , C07K2317/622 , C07K2317/92
摘要: The present invention relates to particularly stable and soluble scFv antibodies and Fab fragments specific for TNF, which comprise specific light chain and heavy chain sequences that are optimized for stability, solubility, in vitro and in vivo binding of TNF, and low immunogenicity. Said antibodies are designed for the diagnosis and/or treatment of TNF-mediated disorders. The nucleic acids, vectors and host cells for expression of the recombinant antibodies of the invention, methods for isolating them and the use of said antibodies in medicine are also disclosed.
摘要翻译: 本发明涉及特别稳定和可溶的scFv抗体和对TNF特异性的Fab片段,其包含针对TNF的稳定性,溶解性,体外和体内结合以及低免疫原性而优化的特异性轻链和重链序列。 所述抗体被设计用于诊断和/或治疗TNF介导的病症。 还公开了用于表达本发明的重组抗体的核酸,载体和宿主细胞,用于分离它们的方法和所述抗体在医学中的用途。
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公开(公告)号:US20110135644A1
公开(公告)日:2011-06-09
申请号:US13000533
申请日:2009-07-10
IPC分类号: A61K39/395 , C07K19/00 , A61P25/00 , A61P25/28 , A61P25/16 , A61P25/18 , A61P25/08 , A61P25/20
CPC分类号: A61K47/183 , A61K9/0043 , A61K9/08 , A61K39/3955 , A61K2039/505 , A61K2039/543 , C07K16/241 , C07K2317/24 , C07K2317/622 , Y02P20/55 , A61K2300/00
摘要: The invention provides compositions and methods that enhance the delivery of large macromolecules (i.e., greater than 10 kDa), such as antigen-binding polypeptides, across tight junctions. Such methods and compositions are particularly useful for delivering therapeutic antigen-binding polypeptides to the CNS, via intranasal administration, for the treatment of neurological disorders.
摘要翻译: 本发明提供了组合物和方法,其增强了穿过紧密连接点的大的大分子(即大于10kDa)的递送,例如抗原结合多肽。 这些方法和组合物特别可用于通过鼻内施用将治疗性抗原结合多肽递送至CNS,用于治疗神经障碍。
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公开(公告)号:US10221237B2
公开(公告)日:2019-03-05
申请号:US15378649
申请日:2016-12-14
发明人: Leonardo Borras , David Urech
摘要: The invention provides methods of using sequence based analysis and rational strategies to improve the solubility of immunobinders, and in particular of single chain antibodies (scFvs). The invention provides methods of engineering immunobinders, and in particular scFvs, by performing one or more substitutions with hydrophilic residues identified by analysis of a database of selected, stable scFv sequences. The invention also provides immunobinders with optimized solubility prepared according to the engineering methods of the invention.
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公开(公告)号:US09908940B2
公开(公告)日:2018-03-06
申请号:US14947133
申请日:2015-11-20
IPC分类号: C07K16/28 , C07K16/22 , C07K16/24 , G01N33/50 , G01N33/566 , C07K16/42 , G01N33/569
CPC分类号: C07K16/2866 , C07K16/22 , C07K16/241 , C07K16/28 , C07K16/4241 , C07K2317/20 , C07K2317/21 , C07K2317/24 , C07K2317/569 , C07K2317/622 , G01N33/5052 , G01N33/566 , G01N33/56972
摘要: The invention provides methods for identifying immunobinders, such as scFv antibodies, capable of specifically binding to cell surface antigens, and compositions identified according to said methods.
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公开(公告)号:US09803027B2
公开(公告)日:2017-10-31
申请号:US14308936
申请日:2014-06-19
发明人: David Urech , Leonardo Jose Borras
CPC分类号: C07K16/42 , C07K16/241 , C07K2317/24 , C07K2317/34 , C07K2317/622 , C07K2317/76
摘要: A method for decreasing the immunogenicity of antibody variable domains is disclosed.
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