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公开(公告)号:US20240255503A1
公开(公告)日:2024-08-01
申请号:US18565377
申请日:2022-05-25
发明人: Thomas HALLAM , Kevin MARCHBANK , David KAVANAGH , Claire HARRIS
IPC分类号: G01N33/564 , C07K14/47 , G01N33/543
CPC分类号: G01N33/564 , C07K14/472 , G01N33/54373 , G01N2333/4716
摘要: Aspects of the present invention relate to the detection of binding events associated with a protein complex comprised of a protease deficient Complement Factor I (FI) protein. Certain embodiments of the present invention provide for a protein complex comprising a Complement Factor I, C3b and further comprising at least one other protein from Complement Factor H (FH), Factor-H-like protein 1 (FHL-1), soluble membrane cofactor protein (sMCP), and soluble complement receptor 1 (sCR1), wherein the Complement Factor I comprises at least one mutation that causes inactivation of Complement Factor I protease activity. Further embodiments of the present invention provide for a protein complex comprising a Complement Factor I, C4b and further comprising at least one other protein from soluble complement receptor 1 (sCR1), soluble membrane cofactor protein (sMCP) and C4b binding protein (C4bp), wherein the Complement Factor I comprises at least one mutation that causes inactivation of Complement Factor I protease activity.
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公开(公告)号:US11879008B2
公开(公告)日:2024-01-23
申请号:US17339021
申请日:2021-06-04
申请人: Q32 Bio Inc.
发明人: Michael Steven Curtis , Michael Storek , Shelia Marie Violette , Susan L. Kalled , Kelly C. Fahnoe , Cheng Ran Huang , Ellen Garber Stark , Frederick Robbins Taylor , Justin Andrew Caravella , Vernon Michael Holers
CPC分类号: C07K16/18 , A61K38/1725 , A61P13/12 , C07K14/472 , C07K2317/51 , C07K2317/565 , C07K2319/00
摘要: Provided herein are fusion protein constructs that can bind a complement-associated antigen, comprising a targeting moiety and a complement modulator protein, or a fragment thereof or a variant thereof. The targeting moiety is an antibody or an antigen binding fragment thereof, in some examples. Further provided are methods of using the fusion protein constructs, for example, in treating complement mediation conditions.
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公开(公告)号:US11807666B2
公开(公告)日:2023-11-07
申请号:US18059929
申请日:2022-11-29
IPC分类号: C07K1/18 , B01J41/20 , B01D15/36 , B01D15/38 , A61K38/36 , A61K38/48 , A61K35/16 , C12N9/64 , B01D15/34 , C07K14/47 , C07K14/755 , C07K14/765 , C07K16/00 , A61K38/00
CPC分类号: C07K1/18 , A61K35/16 , A61K38/36 , A61K38/4846 , B01D15/34 , B01D15/363 , B01D15/3847 , B01J41/20 , C07K14/472 , C07K14/755 , C07K14/765 , C07K16/00 , C12N9/644 , C12N9/6424 , C12Y304/21022 , A61K38/00
摘要: The present invention relates to the field of chromatography. More closely, the invention relates to a chromatographic method for purification of proteins, such as Factor VIII, von Willebrand factor and Factor IX. The chromatographic method is performed on a matrix comprising an inner porous core and outer porous lid surrounding said core.
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公开(公告)号:US20230287051A1
公开(公告)日:2023-09-14
申请号:US18016490
申请日:2021-07-15
申请人: ZP SPV 3 K/S
CPC分类号: C07K7/08 , A61P37/06 , C07K14/472
摘要: Compstatin analogues having improved physicochemical properties, such as increased stability and/or solubility as compared to the 13 amino acid compstatin peptide are described, in particular compstatin analogues that additionally possess useful binding and complement-inhibiting activity. These analogues have an alkylene bridge between sulphur atoms of cysteine residues and include variants with an isoleucine residue at position 3 in place of the wild type valine residue, which provides compstatin peptides with improved binding and complement-inhibiting activity and also enables the introduction of other modifications, for example modifications that are capable of increasing stability, such as the introduction of lysine or serine at position 11.
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公开(公告)号:US20190248839A1
公开(公告)日:2019-08-15
申请号:US16386179
申请日:2019-04-16
IPC分类号: C07K7/64 , A61K47/64 , C07K14/475 , G01N33/564 , C07K14/005 , C12N7/00 , C07K14/47 , C07K7/08
CPC分类号: C07K7/64 , A61K38/00 , A61K47/645 , C07K7/08 , C07K14/005 , C07K14/472 , C07K14/475 , C07K2319/01 , C07K2319/10 , C12N7/00 , C12N2740/16022 , C12N2740/16033 , G01N33/564 , G01N2333/4716
摘要: In some aspects, the present invention cell-penetrating compstatin analog and compositions comprising cell-penetrating compstatin analog. In some aspects, the invention further provides methods of using cell-penetrating compstatin analogs treat a complement-mediated disorder, e.g., to inhibit complement-mediated damage to a cell, tissue, or organ, to inhibit production or release of biologically active C3 cleavage products.
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公开(公告)号:US20190202900A1
公开(公告)日:2019-07-04
申请号:US16256100
申请日:2019-01-24
申请人: INFLARX GMBH
CPC分类号: C07K16/18 , A61K2039/505 , C07K14/472 , C07K2317/24 , C07K2317/34 , C07K2317/565 , C07K2317/76
摘要: The present invention relates to inhibitors of C5a for use in the treatment of pneumonia, especially viral pneumonia. The invention also relates to the use of inhibitors of C5a in the preparation of a pharmaceutical composition for the treatment of pneumonia, especially viral pneumonia. The inventors further relates to methods for the treatment of pneumonia, especially viral pneumonia, comprising the step of administering a therapeutic amount of an inhibitor of C5a to a subject in need thereof.
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公开(公告)号:US20190202878A1
公开(公告)日:2019-07-04
申请号:US16311711
申请日:2017-06-28
申请人: UNIVERSITAT ULM
IPC分类号: C07K14/47
CPC分类号: C07K14/472 , A61K38/00
摘要: The present invention relates to a multi-domain polypeptide comprising (i) a first complement control protein repeat (CCP)-comprising domain being a convertase decay accelerating domain for convertases of the classical and alternative pathways of complement activation, (ii) a host cell recognition domain, and (iii) a second CCP-comprising domains with cofactor activity. The present invention further relates to a polynucleotide encoding said multi-domain polypeptide, to a vector comprising said polynucleotide, and to a host cell comprising said polynucleotide and/or said vector. Further, the present invention relates to the multi-domain polypeptide, the polypeptide, and the vector for use in medicine and for treating and/or preventing inappropriate complement activation and/or a disease having inappropriate complement activation as a symptom. Moreover, the present invention relates to methods and uses related to multi-domain polypeptide, the polypeptide, and the vector.
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公开(公告)号:US10035848B2
公开(公告)日:2018-07-31
申请号:US15110577
申请日:2015-01-08
申请人: The United States of America, as represented by the Secretary, Department of Health and Human Services , University of Virginia Patent Foundation
发明人: Adrian U. Wiestner , Martin W. Skarzynski , Margaret A. Lindorfer , Ronald P. Taylor , Christoph Rader , Berengere Vire
IPC分类号: A61K39/395 , C07K16/18 , C07K16/30 , C07K14/47 , C07K14/725 , A61K39/00
CPC分类号: C07K16/18 , A61K2039/505 , C07B2200/11 , C07K14/472 , C07K14/7051 , C07K16/3061 , C07K2317/24 , C07K2317/34 , C07K2317/51 , C07K2317/515 , C07K2317/565 , C07K2317/73 , C07K2317/732 , C07K2317/734 , C07K2317/92 , C07K2319/03
摘要: An anti-C3d antibody or antibody fragment; method for use thereof to kill cancer cells; and related methods and compositions.
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9.
公开(公告)号:US20180184629A1
公开(公告)日:2018-07-05
申请号:US15736951
申请日:2016-06-16
IPC分类号: A01K67/027 , A61K49/00 , C12N15/90
CPC分类号: A01K67/0275 , A01K67/027 , A01K67/0271 , A01K2207/12 , A01K2207/15 , A01K2217/07 , A01K2227/105 , A01K2267/0387 , A61K49/0008 , C07K14/472 , C12N15/907
摘要: The present invention relates generally to genetically modified non-human animals and immunodeficient non-human animals characterized by restored complement-dependent cytotoxicity, as well as methods and compositions for assessment of therapeutic antibodies in the genetically modified immunodeficient non-human animals. In specific aspects, the present invention relates to immunodeficient non-obese diabetic (NOD), A/J, A/He, AKR, DBA/2, NZB/BIN, B10.D2/oSn and other mouse strains genetically modified to restore complement-dependent cytotoxicity which is lacking in the unmodified immunodeficient mice. In further specific aspects, the present invention relates to NOD.Cg-Prkdcscid IL2rgtm1Wj1/SzJ (NSG), NOD. Cg-Rag1tm1Mom IL2rgtm1Wj1/SzJ (NRG) and NOD.Cg-Prkdcscid IL2rgtm1Wj1/JicTAc (NOG) mice genetically modified to restore complement-dependent cytotoxicity which is lacking in unmodified NSG, NRG and NOG mice. Methods for assessment of therapeutic antibodies or putative therapeutic antibodies in the genetically modified immunodeficient mice characterized by an intact complement system are provided according to specific aspects of the present invention.
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公开(公告)号:US09815890B2
公开(公告)日:2017-11-14
申请号:US13805522
申请日:2011-06-22
IPC分类号: C07K16/28 , A61K39/395 , C07K16/18 , C07K14/47
CPC分类号: C07K16/18 , C07K14/472 , C07K2317/33 , C07K2317/76 , C07K2317/92 , C07K2319/00
摘要: The present invention relates to methods and materials for modulating the complement alternative pathway (CAP), the complement classical pathway (CCP), the complement lectin/mannose pathway (CMP), or combinations thereof, as well as methods and materials for targeting diagnostic, prophylactic and therapeutic agents to localized areas of tissue within the body where they may more directly exert their effects upon the intended target cells or tissue, with reduced, associated systemic effects compared with administration of the same or similar agents in an untargeted, systemic manner. The methods and materials of the present invention may therefore allow for increased efficacy, lower threshold effective dosages and/or lower effective maintenance doses, and/or reduced associated undesired or adverse effects in terms of frequency or severity of occurrence, or both. The present invention also relates to methods and materials for modulating a host humoral immune response, especially reducing, inhibiting, or preventing a host humoral immune response.
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