CA2913155A1 - Engineered heme-binding compositions and uses thereof - Google Patents
Engineered heme-binding compositions and uses thereofInfo
- Publication number
- CA2913155A1 CA2913155A1 CA2913155A CA2913155A CA2913155A1 CA 2913155 A1 CA2913155 A1 CA 2913155A1 CA 2913155 A CA2913155 A CA 2913155A CA 2913155 A CA2913155 A CA 2913155A CA 2913155 A1 CA2913155 A1 CA 2913155A1
- Authority
- CA
- Canada
- Prior art keywords
- heme
- molecule
- binding
- domain
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
- C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
- C12N9/2474—Hyaluronoglucosaminidase (3.2.1.35), i.e. hyaluronidase
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/795—Porphyrin- or corrin-ring-containing peptides
- C07K14/805—Haemoglobins; Myoglobins
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
- C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
- C12Y302/01035—Hyaluronoglucosaminidase (3.2.1.35), i.e. hyaluronidase
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
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- Veterinary Medicine (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Epidemiology (AREA)
- Biophysics (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Communicable Diseases (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361825707P | 2013-05-21 | 2013-05-21 | |
| US61/825,707 | 2013-05-21 | ||
| PCT/US2014/038945 WO2014190040A1 (en) | 2013-05-21 | 2014-05-21 | Engineered heme-binding compositions and uses thereof |
Publications (1)
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| CA2913155A1 true CA2913155A1 (en) | 2014-11-27 |
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|---|---|---|---|
| CA2913155A Abandoned CA2913155A1 (en) | 2013-05-21 | 2014-05-21 | Engineered heme-binding compositions and uses thereof |
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| Country | Link |
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| US (4) | US9988617B2 (enExample) |
| EP (3) | EP3848044A1 (enExample) |
| JP (3) | JP6649250B2 (enExample) |
| AU (2) | AU2014268603B2 (enExample) |
| CA (1) | CA2913155A1 (enExample) |
| WO (1) | WO2014190040A1 (enExample) |
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| DK2347775T3 (da) | 2005-12-13 | 2020-07-13 | Harvard College | Skabeloner til celletransplantation |
| CN107648668B (zh) | 2010-10-06 | 2021-06-18 | 哈佛学院董事会 | 用于基于材料的细胞疗法的可注射的成孔水凝胶 |
| US9675561B2 (en) | 2011-04-28 | 2017-06-13 | President And Fellows Of Harvard College | Injectable cryogel vaccine devices and methods of use thereof |
| CN104244929B (zh) | 2012-04-16 | 2017-04-05 | 哈佛学院董事会 | 用于调节免疫反应的介孔二氧化硅组合物 |
| US9988617B2 (en) * | 2013-05-21 | 2018-06-05 | President And Fellows Of Harvard College | Engineered heme-binding compositions and uses thereof |
| WO2015095604A2 (en) | 2013-12-18 | 2015-06-25 | President And Fellows Of Harvard College | Methods and assays relating to circulating tumor cells |
| US10682400B2 (en) | 2014-04-30 | 2020-06-16 | President And Fellows Of Harvard College | Combination vaccine devices and methods of killing cancer cells |
| EP3250250A4 (en) | 2015-01-30 | 2019-05-22 | President and Fellows of Harvard College | PERITUMORAL AND INTRATUMORAL MATERIALS FOR CANCER THERAPY |
| JP7094533B2 (ja) | 2015-04-10 | 2022-07-04 | プレジデント アンド フェローズ オブ ハーバード カレッジ | 免疫細胞捕捉デバイスおよびその製造および使用方法 |
| WO2017024114A1 (en) | 2015-08-06 | 2017-02-09 | President And Fellows Of Harvard College | Improved microbe-binding molecules and uses thereof |
| EP3411475B1 (en) | 2016-02-06 | 2025-08-27 | President and Fellows of Harvard College | Recapitulating the hematopoietic niche to reconstitute immunity |
| MA44252A (fr) * | 2016-02-16 | 2018-12-26 | Harvard College | Vaccins contre des agents pathogènes et leurs procédés de production et d'utilisation |
| CA3024490A1 (en) | 2016-05-16 | 2017-11-23 | President And Fellows Of Harvard College | Aqueous biomolecule coupling on co2-plasma-activated surfaces |
| CN115537372A (zh) | 2016-07-13 | 2022-12-30 | 哈佛学院院长等 | 抗原呈递细胞模拟支架及其制备和使用方法 |
| EP3493842A4 (en) | 2016-08-02 | 2020-07-29 | President and Fellows of Harvard College | BIOMATERIALS TO MODULATE IMMUNE RESPONSES |
| WO2018045145A1 (en) * | 2016-09-02 | 2018-03-08 | Georgetown University | Serologic assay of liver fibrosis |
| US10584146B2 (en) | 2016-12-07 | 2020-03-10 | Uchicago Argonne, Llc | Heme peptide materials for anti-inflammatory regenerative nanobiomedicine |
| WO2020061129A1 (en) | 2018-09-19 | 2020-03-26 | President And Fellows Of Harvard College | Compositions and methods for labeling and modulation of cells in vitro and in vivo |
| KR102865175B1 (ko) * | 2019-12-19 | 2025-09-30 | 악스톤 바이오사이언시스 코퍼레이션 | 초-장기 작용 인슐린-fc 융합 단백질 및 사용 방법 |
Family Cites Families (198)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL154598B (nl) | 1970-11-10 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van laagmoleculire verbindingen en van eiwitten die deze verbindingen specifiek kunnen binden, alsmede testverpakking. |
| US3817837A (en) | 1971-05-14 | 1974-06-18 | Syva Corp | Enzyme amplification assay |
| US3939350A (en) | 1974-04-29 | 1976-02-17 | Board Of Trustees Of The Leland Stanford Junior University | Fluorescent immunoassay employing total reflection for activation |
| US3954623A (en) | 1974-05-28 | 1976-05-04 | Johnson & Johnson | Blood filtration unit |
| US3996345A (en) | 1974-08-12 | 1976-12-07 | Syva Company | Fluorescence quenching with immunological pairs in immunoassays |
| JPS5418198A (en) * | 1977-07-09 | 1979-02-09 | Toshimitsu Niwa | Artificial intraretinal device |
| US4275149A (en) | 1978-11-24 | 1981-06-23 | Syva Company | Macromolecular environment control in specific receptor assays |
| US4277437A (en) | 1978-04-05 | 1981-07-07 | Syva Company | Kit for carrying out chemically induced fluorescence immunoassay |
| US4340668A (en) | 1979-06-04 | 1982-07-20 | Miles Laboratories, Inc. | Heme-labeled specific binding assay |
| US4366241A (en) | 1980-08-07 | 1982-12-28 | Syva Company | Concentrating zone method in heterogeneous immunoassays |
| US4425330A (en) | 1981-05-20 | 1984-01-10 | Cornell Research Foundation, Inc. | Bovine mastitis vaccine and method for detecting efficacy thereof |
| US4517090A (en) | 1982-03-30 | 1985-05-14 | Baxter Travenol Laboratories, Inc. | Low volume, large area filters for IV or blood filtration |
| US4737462A (en) | 1982-10-19 | 1988-04-12 | Cetus Corporation | Structural genes, plasmids and transformed cells for producing cysteine depleted muteins of interferon-β |
| JPS60500548A (ja) | 1982-12-03 | 1985-04-18 | イ−・アイ・デユポン・ド・ネモア−ス・アンド・コンパニ− | 発色性支持体免疫測定法 |
| WO1984002193A1 (en) | 1982-12-03 | 1984-06-07 | Du Pont | Chromogenic support immunoassay |
| US4518584A (en) | 1983-04-15 | 1985-05-21 | Cetus Corporation | Human recombinant interleukin-2 muteins |
| US5139941A (en) | 1985-10-31 | 1992-08-18 | University Of Florida Research Foundation, Inc. | AAV transduction vectors |
| US5219740A (en) | 1987-02-13 | 1993-06-15 | Fred Hutchinson Cancer Research Center | Retroviral gene transfer into diploid fibroblasts for gene therapy |
| JPH0718875B2 (ja) | 1987-06-19 | 1995-03-06 | ヤマサ醤油株式会社 | 血中または体液中の微量物質含有量の測定法 |
| US5270199A (en) | 1987-08-20 | 1993-12-14 | The Children's Medical Center Corporation | Human mannose-binding protein |
| WO1989001519A1 (en) | 1987-08-20 | 1989-02-23 | Children's Hospital Corporation | Human mannose binding protein |
| DE10399032I1 (de) | 1987-08-28 | 2004-01-29 | Health Research Inc | Rekombinante Viren. |
| ATE122568T1 (de) | 1989-01-25 | 1995-06-15 | Commw Scient Ind Res Org | Polypeptide, antigene oder vakzine gegen babesiosis. |
| US6673776B1 (en) | 1989-03-21 | 2004-01-06 | Vical Incorporated | Expression of exogenous polynucleotide sequences in a vertebrate, mammal, fish, bird or human |
| US5703055A (en) | 1989-03-21 | 1997-12-30 | Wisconsin Alumni Research Foundation | Generation of antibodies through lipid mediated DNA delivery |
| US5693622A (en) | 1989-03-21 | 1997-12-02 | Vical Incorporated | Expression of exogenous polynucleotide sequences cardiac muscle of a mammal |
| US6214804B1 (en) | 1989-03-21 | 2001-04-10 | Vical Incorporated | Induction of a protective immune response in a mammal by injecting a DNA sequence |
| US5137810A (en) | 1989-04-26 | 1992-08-11 | The University Of North Carolina | Method of determining the gram sign of bacteria |
| FR2658432B1 (fr) | 1990-02-22 | 1994-07-01 | Medgenix Group Sa | Microspheres pour la liberation controlee des substances hydrosolubles et procede de preparation. |
| US5981276A (en) | 1990-06-20 | 1999-11-09 | Dana-Farber Cancer Institute | Vectors containing HIV packaging sequences, packaging defective HIV vectors, and uses thereof |
| US5252701A (en) | 1990-07-06 | 1993-10-12 | American Cyanamid Company | Segmented absorbable copolymer |
| DE69131576T2 (de) | 1990-07-30 | 2000-03-16 | Novartis Ag | Insektizide proteine |
| MY109299A (en) | 1990-08-15 | 1996-12-31 | Virogenetics Corp | Recombinant pox virus encoding flaviviral structural proteins |
| GB9020075D0 (en) | 1990-09-14 | 1990-10-24 | Filler Aaron G | Contrast agents for magnetic resonance imaging of axonal transport |
| JPH04130274A (ja) | 1990-09-20 | 1992-05-01 | Kyoto Ikagaku Kenkyusho:Kk | 糖蛋白の分析,検出方法 |
| US5783179A (en) | 1991-08-09 | 1998-07-21 | Syntex (U.S.A.) Inc. | C-reactive protein fragment with immunomodulatory activity |
| EP0616535B1 (en) | 1991-11-27 | 2000-02-02 | Immtech International Incorporated | Method of treating viral infections |
| US5405832A (en) | 1991-11-27 | 1995-04-11 | Immtech International Inc. | Method of treating non-streptococcal bacterial infections |
| US5874238A (en) | 1993-02-26 | 1999-02-23 | Immtech International Inc. | Mutant protein and methods and materials for making and using it |
| US5283238A (en) | 1992-04-24 | 1994-02-01 | Immtech International, Inc. | Methods of treating cancer using modified C-reactive protein |
| US6132419A (en) | 1992-05-22 | 2000-10-17 | Genetronics, Inc. | Electroporetic gene and drug therapy |
| US6703219B1 (en) | 1993-02-26 | 2004-03-09 | Immtech International Inc. | Mutant protein and methods and materials for making and using it |
| US5993434A (en) | 1993-04-01 | 1999-11-30 | Genetronics, Inc. | Method of treatment using electroporation mediated delivery of drugs and genes |
| US5565215A (en) | 1993-07-23 | 1996-10-15 | Massachusettes Institute Of Technology | Biodegradable injectable particles for imaging |
| US5543158A (en) | 1993-07-23 | 1996-08-06 | Massachusetts Institute Of Technology | Biodegradable injectable nanoparticles |
| IT1271486B (it) | 1993-10-12 | 1997-05-28 | Italfarmaco Spa | Oligopeptidi immunomodulatori derivati di frammenti della proteina c- reattiva |
| US5665557A (en) | 1994-11-14 | 1997-09-09 | Systemix, Inc. | Method of purifying a population of cells enriched for hematopoietic stem cells populations of cells obtained thereby and methods of use thereof |
| AUPN214095A0 (en) | 1995-04-03 | 1995-04-27 | Australian Water Technologies Pty Ltd | Method for detecting microorganisms using flow cytometry |
| US5763270A (en) | 1995-06-07 | 1998-06-09 | Genemedicine, Inc. | Plasmid for delivery of nucleic acids to cells and methods of use |
| EP1445322B2 (en) | 1995-06-15 | 2012-06-06 | Crucell Holland B.V. | Packaging systems for human recombinant adenovirus to be used in gene therapy |
| US6001650A (en) | 1995-08-03 | 1999-12-14 | Avigen, Inc. | High-efficiency wild-type-free AAV helper functions |
| US5622856A (en) | 1995-08-03 | 1997-04-22 | Avigen | High efficiency helper system for AAV vector production |
| WO1997014809A2 (en) | 1995-10-16 | 1997-04-24 | Dana-Farber Cancer Institute | Novel expression vectors and methods of use |
| US6004797A (en) | 1995-11-09 | 1999-12-21 | Avigen, Inc. | Adenovirus helper-free recombinant AAV Virion production |
| CA2249354A1 (en) | 1996-03-28 | 1997-10-02 | Genitrix, L.L.C. | Opsonin-enhanced cells, and methods of modulating an immune response to an antigen |
| ZA973051B (en) | 1996-04-24 | 1998-10-12 | Genentech Inc | Type c lectins |
| US6117977A (en) | 1996-04-24 | 2000-09-12 | Genentech, Inc. | Type C lectins |
| FR2751229B1 (fr) | 1996-07-19 | 1998-11-27 | Rhone Merieux | Formule de vaccin polynucleotidique notamment contre la pathologie respiratoire des bovins |
| US5980948A (en) | 1996-08-16 | 1999-11-09 | Osteotech, Inc. | Polyetherester copolymers as drug delivery matrices |
| US6294170B1 (en) | 1997-08-08 | 2001-09-25 | Amgen Inc. | Composition and method for treating inflammatory diseases |
| US6048551A (en) | 1997-03-27 | 2000-04-11 | Hilfinger; John M. | Microsphere encapsulation of gene transfer vectors |
| IL132120A0 (en) | 1997-04-03 | 2001-03-19 | Guilford Pharm Inc | Biodegradable terephthalate polyester-poly (phosphate) polymers compositions articles and methods for making and using the same |
| US6233483B1 (en) | 1997-05-14 | 2001-05-15 | Pacesetter, Inc. | System and method for generating a high efficiency biphasic defibrillation waveform for use in an implantable cardioverter/defibrillator (ICD). |
| US6117100A (en) | 1997-06-06 | 2000-09-12 | Powers; Kathleen M. | Hemodialysis-double dialyzers in parallel |
| IL121191A0 (en) | 1997-06-29 | 1997-11-20 | Yeda Res & Dev | Synthetic peptides and pharmaceutical compositions comprising them |
| US6045925A (en) | 1997-08-05 | 2000-04-04 | Kansas State University Research Foundation | Encapsulated nanometer magnetic particles |
| JPH11206378A (ja) | 1998-01-23 | 1999-08-03 | Fuso Pharmaceutical Industries Ltd | 組換えヒトマンナン結合タンパク質およびその製造方法 |
| US7049099B2 (en) | 1998-01-23 | 2006-05-23 | Fuso Pharmaceutical Industries, Ltd. | Recombinant human mannan-binding proteins and producing method of the same |
| US6528624B1 (en) | 1998-04-02 | 2003-03-04 | Genentech, Inc. | Polypeptide variants |
| JP3898834B2 (ja) | 1998-04-10 | 2007-03-28 | 富士フイルム株式会社 | 血液連続濾過装置 |
| US6007557A (en) | 1998-04-29 | 1999-12-28 | Embol-X, Inc. | Adjustable blood filtration system |
| JP4707231B2 (ja) | 1998-06-10 | 2011-06-22 | スタテンズ セーラム インスティテュート | マンナン結合レクチンを製造するための精製方法及びmbl医薬品 |
| US6800484B2 (en) | 1998-06-24 | 2004-10-05 | Genetronics, Inc. | High efficiency transfection based on low electric field strength, long pulse length |
| CA2338989C (en) | 1998-07-31 | 2010-07-27 | Asahi Kasei Kogyo Kabushiki Kaisha | Antibodies for detecting microorganisms |
| US6419709B1 (en) | 1998-10-02 | 2002-07-16 | Guilford Pharmaceuticals, Inc. | Biodegradable terephthalate polyester-poly(Phosphite) compositions, articles, and methods of using the same |
| US6153212A (en) | 1998-10-02 | 2000-11-28 | Guilford Pharmaceuticals Inc. | Biodegradable terephthalate polyester-poly (phosphonate) compositions, articles, and methods of using the same |
| US6660843B1 (en) * | 1998-10-23 | 2003-12-09 | Amgen Inc. | Modified peptides as therapeutic agents |
| EP1148885A4 (en) | 1999-02-08 | 2002-05-08 | Chiron Corp | ELECTRICALLY INDUCED INCREASE IN IMMUNITY AND EFFECTIVENESS OF IN VIVO DNA VACCINES |
| US6254567B1 (en) | 1999-02-26 | 2001-07-03 | Nxstage Medical, Inc. | Flow-through peritoneal dialysis systems and methods with on-line dialysis solution regeneration |
| DK1168934T3 (da) | 1999-04-12 | 2008-05-13 | Cornell Res Foundation Inc | Hydrogeldannende system med hydrofobe og hydrofile komponenter |
| AU781135B2 (en) | 1999-05-14 | 2005-05-05 | Thomas Vorup Jensen | Recombinant human mannan-binding lectin |
| JP4944324B2 (ja) | 1999-07-13 | 2012-05-30 | ボルダー バイオテクノロジー, インコーポレイテッド | 免疫グロブリン融合タンパク質 |
| US6503761B1 (en) | 1999-10-19 | 2003-01-07 | Kimberly-Clark Worldwide, Inc. | Selective removal of contaminants from a surface using articles having magnets |
| ATE336514T1 (de) | 2000-02-11 | 2006-09-15 | Merck Patent Gmbh | Steigerung der zirkulierenden halbwertzeit von auf antikörpern basierenden fusionsproteinen |
| US6471968B1 (en) | 2000-05-12 | 2002-10-29 | Regents Of The University Of Michigan | Multifunctional nanodevice platform |
| US6503538B1 (en) | 2000-08-30 | 2003-01-07 | Cornell Research Foundation, Inc. | Elastomeric functional biodegradable copolyester amides and copolyester urethanes |
| JP2002165591A (ja) | 2000-09-25 | 2002-06-11 | Jsr Corp | 磁性粒子およびその使用方法 |
| AU2002227184A1 (en) | 2000-10-18 | 2002-04-29 | The Board Of Trustess Of The Leland Stanford Junior University | Methods for development and use of diagnostic and therapeutic agents |
| ATE530212T1 (de) | 2001-04-26 | 2011-11-15 | Asahi Kasei Medical Co Ltd | Blutfiltrationsmethode |
| CA2450123C (en) | 2001-08-02 | 2013-01-29 | Cornell Research Foundation, Inc. | Biodegradable polyhydric alcohol esters |
| GB0119274D0 (en) | 2001-08-08 | 2001-10-03 | Univ Durham | Fusion proteins for insect control |
| US6900292B2 (en) | 2001-08-17 | 2005-05-31 | Lee-Hwei K. Sun | Fc fusion proteins of human erythropoietin with increased biological activities |
| US7396662B2 (en) | 2001-12-19 | 2008-07-08 | Immunex Corporation | C-type lectin polypeptides |
| US6676729B2 (en) | 2002-01-02 | 2004-01-13 | International Business Machines Corporation | Metal salt reduction to form alloy nanoparticles |
| EP1335003A3 (en) | 2002-02-06 | 2004-04-07 | Toyo Boseki Kabushiki Kaisha | Magnetic carrier capable of binding with protein and purification method of protein utilizing the magnetic carrier |
| WO2003066003A2 (en) | 2002-02-07 | 2003-08-14 | Massachusetts Institute Of Technology | Anti-pathogen treatements |
| EP1339075A1 (en) | 2002-02-25 | 2003-08-27 | Motorola, Inc. | Magnetic nanomaterials and synthesis method |
| US6878445B2 (en) | 2002-03-08 | 2005-04-12 | Fuji Photo Film Co., Ltd. | Nanoparticle coated material and production method of same |
| JP2005526084A (ja) | 2002-03-15 | 2005-09-02 | ナットイムネ・アクティーゼルスカブ | マンノース結合レクチンを含む医薬組成物 |
| US20030180814A1 (en) | 2002-03-21 | 2003-09-25 | Alastair Hodges | Direct immunosensor assay |
| US7211396B2 (en) | 2002-04-18 | 2007-05-01 | Antibodyshop A/S | Antibody pairs and kits for immunochemical determination of mannan-binding lectin |
| WO2003090774A1 (en) | 2002-04-24 | 2003-11-06 | The Council Of The Queensland Institute Of Medical Research | Mannose binding lectin and uses thereof |
| US20040018611A1 (en) | 2002-07-23 | 2004-01-29 | Ward Michael Dennis | Microfluidic devices for high gradient magnetic separation |
| US7629440B2 (en) | 2002-08-20 | 2009-12-08 | Genitrix, Llc | Lectin compositions and methods for modulating an immune response to an antigen |
| AP2005003234A0 (en) | 2002-08-20 | 2005-03-31 | Genitrix Llc | Lectin compositions and methods for modulating an immune response to an antigen. |
| CN1694961A (zh) | 2002-09-10 | 2005-11-09 | 内蒂穆恩公司 | 胶原凝集素-补体激活蛋白嵌合体 |
| GB2393728A (en) | 2002-10-04 | 2004-04-07 | Nanomagnetics Ltd | Magnetic nanoparticles |
| EP1417965A1 (en) | 2002-11-07 | 2004-05-12 | Vereniging Voor Christelijk Wetenschappelijk Onderwijs | C-type lectin binding molecules, identification and uses thereof |
| RU2353399C2 (ru) | 2003-01-17 | 2009-04-27 | Этлон Медикал, Инк. | Способ удаления вирусов из крови посредством лектин-аффинного гемодиализа |
| DE10331439B3 (de) | 2003-07-10 | 2005-02-03 | Micromod Partikeltechnologie Gmbh | Magnetische Nanopartikel mit verbesserten Magneteigenschaften |
| US20050014932A1 (en) | 2003-05-15 | 2005-01-20 | Iogenetics, Llc | Targeted biocides |
| DE10325752A1 (de) | 2003-06-06 | 2004-12-30 | Faustus Forschungs Cie. Translational Cancer Research Gmbh | Lektin-Konjugate |
| GB0313259D0 (en) | 2003-06-09 | 2003-07-16 | Consejo Superior Investigacion | Magnetic nanoparticles |
| US7396589B2 (en) | 2003-07-31 | 2008-07-08 | Industrial Technology Research Institute | Core-shell magnetic nanoparticles comprising an inner-transition element |
| TW593158B (en) | 2003-07-31 | 2004-06-21 | Ind Tech Res Inst | Magnetic nanoparticle |
| WO2005027916A1 (en) | 2003-09-19 | 2005-03-31 | Pfizer Products Inc. | Pharmaceutical compositions and methods comprising combinations of 2-alkylidene-19-nor-vitamin d derivatives and aromatase inhibitors |
| US7332096B2 (en) | 2003-12-19 | 2008-02-19 | Fenwal, Inc. | Blood filter assembly having multiple filtration regions |
| KR20060124656A (ko) | 2003-12-31 | 2006-12-05 | 메르크 파텐트 게엠베하 | 개선된 약물동태를 가지는 Fc-에리스로포이에틴 융합단백질 |
| EP2053062A1 (en) | 2004-03-24 | 2009-04-29 | Xencor, Inc. | Immunoglobin variants outside the Fc region |
| US7488302B1 (en) | 2004-03-29 | 2009-02-10 | Robert Helm | Device allowing serial use of clean and alternative blood filters during blood filtration |
| SE0401033D0 (sv) | 2004-04-20 | 2004-04-20 | Amersham Biosciences Ab | Device and method for protein analysis |
| WO2007001332A2 (en) | 2004-08-04 | 2007-01-04 | University Of Massachusetts | Anti-pathogen immunoadhesins |
| JP2008515389A (ja) * | 2004-08-20 | 2008-05-15 | ノボ ノルディスク アクティーゼルスカブ | ヘモペキシン融合タンパク質 |
| JP4731875B2 (ja) | 2004-10-15 | 2011-07-27 | 東洋紡績株式会社 | 血液浄化器の滅菌方法および血液浄化器包装体 |
| DK1800136T3 (da) | 2004-10-15 | 2012-03-26 | Danisco Us Inc | Kompetitiv differentiel screening |
| MX2007005107A (es) | 2004-10-28 | 2007-09-11 | Dobeel Co Ltd | Metodo para la produccion masiva de lectina de union a manosa multimerica. |
| US20060141547A1 (en) | 2004-11-16 | 2006-06-29 | Das Hasi R | Novel diagnostic marker, a diagnostic kit and a method for diagnosis of rheumatoid arthritis |
| US7172906B2 (en) | 2004-11-16 | 2007-02-06 | Dade Behring Inc. | Reduction of non-specific binding in assays |
| US8084275B2 (en) | 2005-02-08 | 2011-12-27 | Fujifilm Corporation | Magnetic composite body, production method thereof, method for removing substance with mannose on its surface, and method for concentrating substance with mannose on its surface |
| US7462446B2 (en) | 2005-03-18 | 2008-12-09 | University Of Washington | Magnetic nanoparticle compositions and methods |
| US7700193B2 (en) | 2005-04-08 | 2010-04-20 | Industrial Technology Research Institute | Core-shell structure with magnetic, thermal, and optical characteristics and manufacturing method thereof |
| CN101193651A (zh) | 2005-04-11 | 2008-06-04 | 内蒂穆恩公司 | 甘露聚糖结合凝集素(mbl)在治疗与癌症相关的免疫削弱的病症中的用途 |
| US20070031819A1 (en) | 2005-04-26 | 2007-02-08 | University Of Washington | Microfluidic systems for biological and molecular analysis and methods thereof |
| US20070231833A1 (en) | 2005-05-23 | 2007-10-04 | Arcidiacono Steven M | Labeled antimicrobial peptides and method of using the same to detect microorganisms of interest |
| JP2007002557A (ja) | 2005-06-24 | 2007-01-11 | Kensetsu Kiso Eng Co Ltd | 張出し道路 |
| TWI333959B (en) | 2005-08-31 | 2010-12-01 | Academia Sinica | Methods and reagents for the analysis and purification of polysaccharides |
| US20070264199A1 (en) | 2005-09-26 | 2007-11-15 | Labhasetwar Vinod D | Magnetic nanoparticle composition and methods for using the same |
| AU2006299414A1 (en) | 2005-09-30 | 2007-04-12 | Caliper Life Sciences, Inc. | Microfluidic device for purifying a biological component using magnetic beads |
| US9220831B2 (en) | 2005-10-06 | 2015-12-29 | Children's Medical Center Corporation | Device and method for combined microfluidic-micromagnetic separation of material in continuous flow |
| EP2388013A3 (en) | 2005-10-26 | 2012-03-07 | Science & Technology Corporation @ UNM | C-reactive protein and its use to treat systemic Lupus erythematosus and related conditions |
| US20130072445A9 (en) | 2005-10-26 | 2013-03-21 | Terry W. Du Clos | Development of c-reactive protein mutant with improved therapeutic benefit in immune thrombocytopenia and lupus nephritis |
| US20070269818A1 (en) | 2005-12-28 | 2007-11-22 | Affymetrix, Inc. | Carbohydrate arrays |
| US20090181041A1 (en) | 2006-01-23 | 2009-07-16 | Jan Holgersson | Production of proteins carrying oligomannose or human-like glycans in yeast and methods of use thereof |
| EP1979079A4 (en) | 2006-02-03 | 2012-11-28 | Integenx Inc | MICROFLUIDIC DEVICES |
| US8821851B2 (en) | 2006-03-23 | 2014-09-02 | The General Hospital Corporation | Inflammation-inhibitory serum factors and uses thereof |
| WO2007111496A1 (en) | 2006-03-28 | 2007-10-04 | Universiteit Utrecht Holding B.V. | Improved carbohydrate recognition domains |
| US8454934B2 (en) | 2006-05-25 | 2013-06-04 | Canadian Blood Services | High molecular weight chelation structure |
| EP1862541A1 (en) * | 2006-06-01 | 2007-12-05 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Polypeptides derived from the hemopexin-like domain of metalloproteinase MMP-2 |
| KR101343034B1 (ko) | 2006-09-05 | 2013-12-18 | 삼성전자 주식회사 | 원심력 기반의 단백질 검출용 미세유동 장치 및 이를포함하는 미세유동 시스템 |
| US8273310B2 (en) | 2006-09-05 | 2012-09-25 | Samsung Electronics Co., Ltd. | Centrifugal force-based microfluidic device for nucleic acid extraction and microfluidic system including the microfluidic device |
| US8088596B2 (en) | 2006-10-10 | 2012-01-03 | Oakland University | Method of microorganism detection using carbohydrate and lectin recognition |
| WO2009008925A2 (en) | 2007-04-05 | 2009-01-15 | The Regents Of The University Of California | A particle-based microfluidic device for providing high magnetic field gradients |
| US20080260738A1 (en) | 2007-04-18 | 2008-10-23 | Moore Margaret D | Single chain fc, methods of making and methods of treatment |
| WO2008130618A1 (en) | 2007-04-19 | 2008-10-30 | The Charles Stark Draper Laboratory, Inc. | Method and apparatus for separating particles, cells, molecules and particulates |
| BRPI0811857A2 (pt) * | 2007-05-14 | 2014-10-21 | Biogen Idec Inc | Regiões fc (scfc) de cadeia simples, polipeptídeos de aglutinação que as compreendem e métodos relacionados. |
| EP3176264B1 (en) | 2007-05-30 | 2018-09-26 | Postech Academy-Industry- Foundation | Immunoglobulin fusion proteins |
| WO2009033770A2 (en) | 2007-09-11 | 2009-03-19 | Mondobiotech Laboratories Ag | Calcitonin c-terminal flanking peptide for use as a therapeutic agent |
| US8105487B2 (en) | 2007-09-25 | 2012-01-31 | Fresenius Medical Care Holdings, Inc. | Manifolds for use in conducting dialysis |
| EP2207798A2 (en) | 2007-10-29 | 2010-07-21 | Virginia Tech Intellectual Properties, Inc. | Porcine dc-sign, icam-3 and lsectin and uses thereof |
| WO2009062195A2 (en) | 2007-11-09 | 2009-05-14 | Anaphore, Inc. | Fusion proteins of mannose binding lectins for treatment of disease |
| ES2326109B1 (es) | 2007-12-05 | 2010-06-25 | Consejo Superior De Investigaciones Cientificas | Microdispositivo de separacion y extraccion selectiva y no invasiva de particulas en suspensiones polidispersas, procedimiento de fabricacion y sus aplicaciones. |
| US20100266558A1 (en) | 2007-12-18 | 2010-10-21 | Dov Zipori | Method and assay for glycosylation pattern detection related to cell state of stem cells |
| WO2009086343A2 (en) | 2007-12-31 | 2009-07-09 | 3M Innovative Properties Company | Microorganism-capturing compositions and methods |
| WO2009126346A2 (en) | 2008-01-18 | 2009-10-15 | The General Hospital Corporation | Methods for prevention and treatment of infections with supraphysiological doses of mannan-binding lectin (mbl) and ficolin-mbl fusion proteins |
| KR101625979B1 (ko) | 2008-03-28 | 2016-05-31 | 국립대학법인 홋가이도 다이가쿠 | 항 h5 아형 a형 인플루엔자 바이러스 헤마글루티닌 모노클로날 항체 |
| CA2722952A1 (en) | 2008-03-31 | 2009-10-08 | Japan Tobacco Inc. | Quantitation method of virus |
| WO2009123348A1 (ja) | 2008-03-31 | 2009-10-08 | 日本たばこ産業株式会社 | ウイルス濃縮法 |
| US20100323429A1 (en) | 2008-04-10 | 2010-12-23 | Yu-Chen Hu | Methods for purifying baculovirus |
| US8865876B2 (en) | 2008-06-02 | 2014-10-21 | California Institute Of Technology | Engineered lectin oligomers with antiviral activity |
| JP2010122205A (ja) | 2008-08-29 | 2010-06-03 | Sysmex Corp | 麻疹ウイルス検出方法、メンブレンアッセイ用試験具およびメンブレンアッセイ用試験キット |
| US20110159000A1 (en) | 2008-09-05 | 2011-06-30 | The Regents Of The University Of California | Antibodies with mannose binding lectin effector function for inhibiting pathologic inflammatory conditions |
| WO2010033514A1 (en) | 2008-09-17 | 2010-03-25 | Aethlon Medical, Inc. | Methods for reducing viral load of hepatitus c virus in hemodialysis patients |
| WO2010065765A2 (en) | 2008-12-04 | 2010-06-10 | Aethlon Medical, Inc. | Affinity capture of circulating biomarkers |
| CN106243229B (zh) | 2008-12-22 | 2019-09-06 | 国立大学法人北海道大学 | 具有三螺旋结构的蛋白质物质及其制造方法 |
| US8664366B2 (en) | 2009-01-09 | 2014-03-04 | Apogenix Gmbh | Fusion proteins forming trimers |
| EP2396053B1 (en) | 2009-01-15 | 2016-09-28 | Brightwake Limited | Extracorporeal blood filtration |
| AU2010206681A1 (en) * | 2009-01-23 | 2011-09-01 | Biogen Idec Ma Inc. | Stabilized Fc polypeptides with reduced effector function and methods of use |
| AU2010208374A1 (en) | 2009-01-28 | 2011-08-04 | Smartcells, Inc. | Binding-site modified lectins and uses thereof |
| KR101144005B1 (ko) | 2009-11-06 | 2012-05-09 | 주식회사 위노바 | 추간체 고정재 |
| WO2011084749A1 (en) * | 2009-12-21 | 2011-07-14 | The Research Foundation Of State University Of New York | Compositions and methods for inhibiting mmp-9-mediated cell migration |
| WO2011090954A2 (en) | 2010-01-19 | 2011-07-28 | President And Fellows Of Harvard College | Engineered opsonin for pathogen detection and treatment |
| US20130157283A1 (en) | 2010-01-19 | 2013-06-20 | President And Fellows Of Harvard College | Rapid pathogen diagnostic device and method |
| WO2011103144A1 (en) | 2010-02-16 | 2011-08-25 | President And Fellows Of Harvard College | Methods and systems for detection of microbes |
| KR101140029B1 (ko) | 2010-02-23 | 2012-06-21 | 한국식품연구원 | 항원고정화 면역형광 슬라이드의 제조방법 및 그에 의해 제조되는 면역형광 슬라이드 |
| US20130123185A1 (en) * | 2010-08-06 | 2013-05-16 | Emory University | Methods of treating and diagnosing acute chest syndrome |
| WO2012050874A2 (en) * | 2010-09-28 | 2012-04-19 | Soares Miguel P | Targeting heme for the treatment of immune mediated inflammatory diseases |
| US9353646B2 (en) | 2011-01-19 | 2016-05-31 | President And Fellows Of Harvard College | Slippery surfaces with high pressure stability, optical transparency, and self-healing characteristics |
| US8469916B2 (en) | 2011-02-28 | 2013-06-25 | Fenwal, Inc. | Systems and methods for single needle continuous plasma processing |
| CA2831857A1 (en) | 2011-04-01 | 2012-10-04 | Children's Medical Center Corporation | Dialysis like therapeutic (dlt) device |
| ES2608835T3 (es) | 2011-04-13 | 2017-04-17 | Bristol-Myers Squibb Company | Proteínas de fusión Fc que comprenden nuevos enlazadores o disposiciones |
| EP3081937B1 (en) | 2011-07-18 | 2019-11-13 | President and Fellows of Harvard College | Engineered microbe-targeting molecules and uses thereof |
| WO2013049321A1 (en) | 2011-09-28 | 2013-04-04 | The General Hospital Corporation | Use of hemopexin to sequester hemoglobin |
| JP5477401B2 (ja) | 2012-02-03 | 2014-04-23 | 株式会社デンソー | 電子制御装置 |
| AU2013225823A1 (en) | 2012-02-29 | 2014-09-18 | President And Fellows Of Harvard College | Rapid antibiotic susceptibility testing |
| WO2014014788A2 (en) * | 2012-07-18 | 2014-01-23 | President And Fellows Of Harvard College | Modification of surfaces for simulataneous repellency and targeted binding of desired moieties |
| WO2014110368A1 (en) | 2013-01-11 | 2014-07-17 | The California Institute For Biomedical Research | Bovine fusion antibodies |
| WO2014144325A1 (en) | 2013-03-15 | 2014-09-18 | President And Fellows Of Harvard College | Methods and compositions for improving detection and/or capture of a target entity |
| US9988617B2 (en) * | 2013-05-21 | 2018-06-05 | President And Fellows Of Harvard College | Engineered heme-binding compositions and uses thereof |
-
2014
- 2014-05-21 US US14/892,252 patent/US9988617B2/en active Active
- 2014-05-21 WO PCT/US2014/038945 patent/WO2014190040A1/en not_active Ceased
- 2014-05-21 EP EP20213586.9A patent/EP3848044A1/en not_active Withdrawn
- 2014-05-21 JP JP2016515046A patent/JP6649250B2/ja active Active
- 2014-05-21 AU AU2014268603A patent/AU2014268603B2/en active Active
- 2014-05-21 EP EP14801627.2A patent/EP3010522B1/en active Active
- 2014-05-21 EP EP21150097.0A patent/EP3848045A1/en not_active Withdrawn
- 2014-05-21 CA CA2913155A patent/CA2913155A1/en not_active Abandoned
-
2018
- 2018-05-01 US US15/968,116 patent/US10501729B2/en active Active
- 2018-06-08 AU AU2018204114A patent/AU2018204114B2/en active Active
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2019
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2020
- 2020-01-16 JP JP2020005037A patent/JP7121057B2/ja active Active
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2022
- 2022-03-18 US US17/698,576 patent/US11939608B2/en active Active
- 2022-06-01 JP JP2022089365A patent/JP2022107724A/ja active Pending
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| AU2014268603A1 (en) | 2015-12-10 |
| EP3848044A1 (en) | 2021-07-14 |
| AU2018204114B2 (en) | 2019-05-09 |
| JP2022107724A (ja) | 2022-07-22 |
| US10501729B2 (en) | 2019-12-10 |
| JP6649250B2 (ja) | 2020-02-19 |
| EP3010522A1 (en) | 2016-04-27 |
| AU2018204114A1 (en) | 2018-06-28 |
| AU2014268603B2 (en) | 2018-03-22 |
| EP3848045A1 (en) | 2021-07-14 |
| US20180320157A1 (en) | 2018-11-08 |
| US20220267749A1 (en) | 2022-08-25 |
| HK1223560A1 (zh) | 2017-08-04 |
| JP2016520591A (ja) | 2016-07-14 |
| WO2014190040A1 (en) | 2014-11-27 |
| EP3010522B1 (en) | 2021-01-20 |
| US20160090583A1 (en) | 2016-03-31 |
| US20200248158A1 (en) | 2020-08-06 |
| EP3010522A4 (en) | 2017-01-04 |
| US11312949B2 (en) | 2022-04-26 |
| US11939608B2 (en) | 2024-03-26 |
| JP2020090510A (ja) | 2020-06-11 |
| US9988617B2 (en) | 2018-06-05 |
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| HK1223560B (en) | Engineered heme-binding compositions and uses thereof | |
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