HRP20160221T1 - Serum amiloidni p derivati i njihova priprema i upotreba - Google Patents

Serum amiloidni p derivati i njihova priprema i upotreba Download PDF

Info

Publication number
HRP20160221T1
HRP20160221T1 HRP20160221T HRP20160221T HRP20160221T1 HR P20160221 T1 HRP20160221 T1 HR P20160221T1 HR P20160221 T HRP20160221 T HR P20160221T HR P20160221 T HRP20160221 T HR P20160221T HR P20160221 T1 HRP20160221 T1 HR P20160221T1
Authority
HR
Croatia
Prior art keywords
sap polypeptide
polypeptide
linked
amino acid
human sap
Prior art date
Application number
HRP20160221T
Other languages
English (en)
Inventor
W Scott Willett
Richard J Caimi
Original Assignee
Promedior Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Promedior Inc filed Critical Promedior Inc
Publication of HRP20160221T1 publication Critical patent/HRP20160221T1/hr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/04Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Immunology (AREA)
  • Biochemistry (AREA)
  • Zoology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Toxicology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Transplantation (AREA)
  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Neurology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicinal Preparation (AREA)
  • Steroid Compounds (AREA)

Claims (38)

1. Glikolizirani humani serum amiloid P (SAP) polipeptid koji sadržava oligosaharidni lanac vezan na N, naznačen time, da najmanje jedan ogranak oligosaharidnog lanca završava s kiselinskim dijelom sijalične kiseline vezanim na α2,3.
2. Glikozilirani humani SAP polipeptid u skladu s patentnim zahtjevom 1, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 85% identična aminokiselinskoj sekvenci SEQ ID NO: 1.
3. Glikozilirani humani SAP polipeptid u skladu s patentnim zahtjevom 1 ili 2, naznačen time, da oligosaharidni lanac vezan na N sadržava pentasaharidnu jezgru Man[(α1,6-)-(Man(α1,3)]-Man(�1,4)-GlcNAc(�1,4)-GlcNAc(�1,N)-Asn.
4. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 3, naznačen time, da oligosaharidni lanac sadržava najmanje jednu granu koja ima strukturu NeuNAc2a3Gal�4GlcNAc�2Manα6
5. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 4, naznačen time, da je SAP polipeptid rekombinantni polipeptid.
6. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 90% identična aminokiselinskoj sekvenci SEQ ID NO: 1.
7. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 95% identična aminokiselinskoj sekvenci SEQ ID NO: 1.
8. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 96% identična sekvenciji aminokiselina iz SEQ ID'NO: 1.
9. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 98% identična aminokiselinskoj sekvenci SEQ ID NO: 1.
10. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu koja je najmanje 99% identična aminokiselinskoj sekvenci SEQ ID NO: 1.
11. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time, da polipeptid sadržava aminokiselinsku sekvencu SEQ ID NO:1.
12. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 11, naznačen time, da je polipeptid fuzijski protein koji sadržava domenu SAP i jednu ili više heterolognih domena.
13. Glikozilirani humani SAP polipeptid u skladu s patentnim zahtjevom 12, naznačen time, da jedna ili više heterolognih domena povećavaju jedno ili više od sljedećih svojstava: in vivo stabilnost, vrijeme in vivo polu-života, unos/primjenu, tkivnu lokalizaciju ili distribuciju, formiranje proteinskih kompleksa I / ili pročišćavanje.
14. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 13, naznačen time, da polipeptid sadržava jedan ili više modificiranih aminokiselinskih ostataka.
15. Glikozilirani humani SAP polipeptid u skladu s patentnim zahtjevom 14, naznačen time, da jedan ili više modificiranih aminokiselinskih ostataka obuhvaća PEGilirane amilno kiseline, preniliranu amino kiselinu, acetiliranu aminokiselinu, biotiniliranu aminokiselinu, i/ili amino kiselinu konjugiranu na organsko derivatizirajuće sredstvo.
16. Glikozilirani humani SAP polipeptid u skladu s patentnim zahtjevom 15, naznačen time, da jedan amino kiselinski ostatak ili više aminokiselinskih ostataka povećava in vivo stabilnost, vrijeme in vivo polu-života, unos / primjenu, tkivnu lokalizaciju ili distribuciju, formiranje proteinskih kompleksa i / ili pročišćavanje.
17. Farmaceutski pripravak prikladan za upotrebu kod sisavaca, naznačen time, da sadržava humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 16 i farmaceutski prihvatljivu podlogu.
18. Postupak za dobivanje humanog SAP polipeptida koji sadržava oligosaharidni lanac vezan na N, pričemu najmanje jedan ogranak oligosaharidnog lanca završava s kiselinskim dijelom sijalične kiseline vezanim na α2,3, naznačen time, da postupak obuhvaća: i) ekspresiju ljudskog SAP polipeptida u stanici; i ii) izolaciju ljudskog SAP polipeptida iz stanice.
19. Postupak u skladu s patentnim zahtjevom 18, naznačen time, da je stanica CHO stanica.
20. Postupak u skladu s patentnim zahtjevom 18 ili 19, naznačen time, da je SAP polipeptid polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 16.
21. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, 7 ili 12 do 16 ili postupak u skladu s bilo kojim od patentnih zahtjeva 18 do 20, naznačen time, da sve grane oligosaharidnog lanca završavaju s kiselinskim dijelom sijalične kiseline vezanim na α2,3.
22. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 5, 7 ili 12 do 16 ili postupak u skladu s bilo kojim od patentnih zahtjeva 18 do 20, naznačen time, da je oligosaharidni lanac u biti bez kiselinskih ostataka sijalične kiseline vezanih na α2,3.
23. Postupak u skladu s patentnim zahtjevom 18, naznačen time, da nadalje obuhvaća enzimske ili kemijske promjene izoliranog SAP polipeptida da bi se proizveo SAP polipeptid s modificiranim oligosaharidnim lancem.
24. Postupak u skladu s patentnim zahtjevom 23, naznačen time, da enzimski ili kemijski proces promjene izoliranog SAP polipeptida uklanja jednu ili više završnih
25. Postupak u skladu s patentnim zahtjevom 24, naznačen time, da enzimski ili kemijski proces promjene izoliranog SAP polipeptida zamjenjuje jednu ili više završnih skupina sijalične kiselina vezanih na α2,6 oligosaharidnog lanca s jednom ili više skupina sijalične kiselina vezanih na α2,3.
26. Glikozilirani humani SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 16, ili postupak u skladu s bilo kojim od patentnih zahtjeva 18 do 25, naznačen time, da izolirani SAP polipeptid ima IC50 za inhibiciju diferencijacije monocita u fibrocite in vitro koja je manja od jedne polovine odgovarajućeg uzorka divljeg tipa SAP izoliranog iz humanog seruma.
27. Postupak za pripremu humanog SAP polipeptida, naznačen time, da postupak obuhvaća: i) pribavljanje glikoliziranog humanog SAP polipeptida, pri čemu glikozilirani humani SAP polipeptid sadržava oligosaharidni lanac vezan na N ; i ii) enzimsku ili kemijsku promjenu oligosaharidnog lanca vezanog na N humanog SAP polipeptida kako bi se dobio modificirani glikozilirani humani SAP polipeptid, pri čemu barem jedna grana oligosaharidnog lanca završava kiselinskom skupinom sijalične kiseline vezanim na α2,3.
28. Postupak u skladu s patentnim zahtjevom 27, naznačen time, da proces enzimske ili kemijske promjene oligosaharidnog lanca vezanog na N SAP polipeptida uklanja jednu ili više završnih skupina sijalične kiseline vezanih na α2,6 iz oligosaharidnog lanca.
29. Postupak u skladu s patentnim zahtjevom 27, naznačen time, da proces enzimske ili kemijske promjene oligosaharidnog lanca vezanog na N humanog SAP polipeptida zamjenjuje jednu ili više završnih skupina sijalične kiselina vezanih na α2,6 oligosaharidnog lanca s jednom ili više skupina sijalične kiselina vezanih na α2,3.
30. Postupak u skladu s bilo kojim od patentnih zahtjeva 27 do 29, naznačen time, da je oligosaharidni lanac vezan na N ima barem 50% manje ostataka sijalične kiselina vezanih na α.2,6 od divljeg tipa humanog SAP proteina izoliranog iz humanog seruma.
31. Postupak u skladu s bilo kojim od patentnih zahtjeva 27 do 29, naznačen time, da su oligosaharidni lanci vezani na N u biti bez kiselinskih ostataka sijalične kiseline vezanih na α2,6.
32. Postupak u skladu s bilo kojim od patentnih zahtjeva 27 do 31, naznačen time, da svi ogranci oligosaharidnih lanaca završavaju skupinama sijalične kiseline vezanim na α2,3.
33. Postupak u skladu s bilo kojim od patentnih zahtjeva 27 do 32, naznačen time, da modificirana glikolizirani SAP polipeptid ima IC50 za inhibiciju diferencijacije monocita u fibrocite in vitro, koja je manja od jedne polovice one od odgovarajućeg uzorka SAP divljeg tipa izoliranog iz humanog seruma.
34. Postupak za pripremu humanog SAP polipeptida, naznačen time, da obuhvaća: i) pripremu humanog SAP polipeptida i ii) enzimsku ili kemijsku promjenu humanog SAP polipeptida da bi se proizveo glikozilirani humani SAP polipeptid koji sadržava oligosaharide vezane na N, pri čemu barem jedan ogranak oligosaharidnog lanca 2,3 završava skupinom sijalične kiseline vezanom na α2,3.
35. Humani SAP polipeptid koji sadržava oligosaharidni lanac vezan na N , naznačen time, da najmanje jedan ogranak oligosaharlda završava skupinom sijalične kiseline vezanom na α2,3 koji je pripravljen postupkom koji obuhvaća: i) ekspresija SAP polipeptida u CHO stanici; i ii) izolaciju SAP polipeptida iz stanice.
36. Humani SAP polipeptid u skladu s patentnim zahtjevom 35, naznačen time, da SAP polipeptid ima IC50 za inhibiciju diferencijacije monocita u fibrocite in vitro koja je manja od polovine one odgovarajućeg uzorka divljeg tipa SAP izoliranog iz humanog seruma.
37. CHO stanica koja obuhvaća humani SAP polipeptid koji sadržava oligosaharidni lanac vezan na N, naznačen time, da najmanje jedan ogranak oligosahardnog lanca završava kiselinskom skupinom sijalične kiseline vezanim na α2,3.
38. SAP polipeptid u skladu s bilo kojim od patentnih zahtjeva 1 do 16 za uporabu u liječenju ili sprečavanju stanja ili poremećaja odabranih iz skupine koju čine: upalni poremećaji, fibrozni ili fibroproliferativni poremećaji, poremećaji preosjetljivosti, autoimuni poremećaji ili upalni poremećaji sluznice.
HRP20160221T 2009-06-04 2016-03-01 Serum amiloidni p derivati i njihova priprema i upotreba HRP20160221T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US21793109P 2009-06-04 2009-06-04
PCT/US2010/037542 WO2010141918A1 (en) 2009-06-04 2010-06-04 Serum amyloid p derivatives and their preparation and use
EP10784210.6A EP2438083B1 (en) 2009-06-04 2010-06-04 Serum amyloid p derivatives and their preparation and use

Publications (1)

Publication Number Publication Date
HRP20160221T1 true HRP20160221T1 (hr) 2016-03-25

Family

ID=43298203

Family Applications (2)

Application Number Title Priority Date Filing Date
HRP20160221T HRP20160221T1 (hr) 2009-06-04 2016-03-01 Serum amiloidni p derivati i njihova priprema i upotreba
HRP20181803TT HRP20181803T1 (hr) 2009-06-04 2018-10-31 Serumski amiloidni p derivati i njihova priprava i uporaba

Family Applications After (1)

Application Number Title Priority Date Filing Date
HRP20181803TT HRP20181803T1 (hr) 2009-06-04 2018-10-31 Serumski amiloidni p derivati i njihova priprava i uporaba

Country Status (28)

Country Link
US (5) US9296800B2 (hr)
EP (2) EP2438083B1 (hr)
JP (3) JP5801293B2 (hr)
CN (1) CN102574902B (hr)
AU (1) AU2010256426B2 (hr)
BR (2) BR122020010980B1 (hr)
CA (1) CA2764461C (hr)
CO (1) CO6480917A2 (hr)
CR (1) CR20110640A (hr)
CY (1) CY1120817T1 (hr)
DK (2) DK2438083T3 (hr)
EA (1) EA030332B1 (hr)
ES (2) ES2692815T3 (hr)
HK (1) HK1168603A1 (hr)
HR (2) HRP20160221T1 (hr)
HU (1) HUE026737T2 (hr)
IL (1) IL216744A (hr)
LT (1) LT3042915T (hr)
MX (1) MX2011012738A (hr)
MY (1) MY158761A (hr)
NZ (1) NZ596849A (hr)
PL (2) PL2438083T3 (hr)
PT (1) PT3042915T (hr)
SI (2) SI3042915T1 (hr)
TR (1) TR201815592T4 (hr)
UA (1) UA110323C2 (hr)
WO (1) WO2010141918A1 (hr)
ZA (1) ZA201108857B (hr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8247370B2 (en) * 2006-12-04 2012-08-21 Promedior, Inc. Conjoint therapy for treating fibrotic diseases
US20090092574A1 (en) 2006-12-29 2009-04-09 Scott Richard W Ophthalmic And Otic Compositions Of Facially Amphiphilic Polymers And Oligomers And Uses Thereof
US9884899B2 (en) * 2007-07-06 2018-02-06 Promedior, Inc. Methods for treating fibrosis using CRP antagonists
US8497243B2 (en) * 2007-07-06 2013-07-30 Promedior, Inc. Methods and compositions useful in the treatment of mucositis
CA2755047C (en) 2009-03-11 2018-12-04 Promedior, Inc. Treatment methods for autoimmune disorders
JP5797565B2 (ja) * 2009-03-11 2015-10-21 プロメディオール, インコーポレイテッド 過敏性障害(hypersensitive disorder)に対する処置および診断方法
UA110323C2 (en) * 2009-06-04 2015-12-25 Promedior Inc Derivative of serum amyloid p and their receipt and application
ES2552793T3 (es) 2009-06-17 2015-12-02 Promedior Inc. Variantes de SAP y su uso
FR2969153B1 (fr) * 2010-12-17 2014-10-17 Lab Francais Du Fractionnement Procede de purification de proteine amyloide p et utilisation de la proteine ainsi purifiee
WO2012158672A2 (en) 2011-05-16 2012-11-22 Polymedix, Inc. Compounds for use in treatment of mucositis
JP6340319B2 (ja) * 2011-12-21 2018-06-06 プロメディオール, インコーポレイテッド 血清アミロイドp−抗体融合タンパク質
EP3718558A1 (en) * 2013-10-08 2020-10-07 Promedior, Inc. Methods for treating fibrotic cancers
FR3012453B1 (fr) 2013-10-31 2015-11-13 Lab Francais Du Fractionnement Proteine chimerique dans le traitement de l’amylose
CN105372214B (zh) * 2014-08-18 2019-06-28 中国科学院上海有机化学研究所 一种鉴定新红细胞生成刺激蛋白的n-连接寡糖结构的方法
MX2019002734A (es) * 2016-09-13 2019-05-27 Bayer Healthcare Llc Glicoformas del factor viia.
JP6852397B2 (ja) 2016-12-28 2021-03-31 株式会社島津製作所 分析用試料の調製方法および分析方法
CN108114001B (zh) * 2017-12-23 2023-05-30 中国科学院海洋研究所 一种诱导海产双壳贝类产卵的诱导剂及其应用方法
WO2021248008A1 (en) 2020-06-05 2021-12-09 Innovation Pharmaceuticals Inc. Arylamide compounds for treatment and prevention of viral infections
IL302388A (en) * 2020-11-02 2023-06-01 Attralus Inc SAP FC fusion proteins and methods of use

Family Cites Families (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1562244A (en) * 1976-11-11 1980-03-05 Lock P M Wound dressing materials
GB1594389A (en) * 1977-06-03 1981-07-30 Max Planck Gesellschaft Dressing material for wounds
GB8516081D0 (en) 1985-06-25 1985-07-31 Ciba Geigy Ag Assay & purification of amyloid components
US6071517A (en) * 1986-07-07 2000-06-06 Medarex, Inc. Bispecific heteroantibodies with dual effector functions
EP0321703B1 (en) * 1987-11-20 1993-04-28 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Absorbent for serum amyloid protein
US7070994B2 (en) * 1988-03-21 2006-07-04 Oxford Biomedica (Uk) Ltd. Packaging cells
US5047335A (en) 1988-12-21 1991-09-10 The Regents Of The University Of Calif. Process for controlling intracellular glycosylation of proteins
US5092876A (en) * 1989-08-30 1992-03-03 The United States Of America As Represented By The Department Of Health And Human Services Cell attachment peptides derived from amyloid P component
EP0587777A4 (en) 1991-05-31 1995-05-10 New England Deaconess Hospital CARCINOBRYONARY ANTIGEN BINDING PROTEINS AND METHODS OF ISOLATING AND USING THE SAME.
US5591709A (en) * 1991-08-30 1997-01-07 Life Medical Sciences, Inc. Compositions and methods for treating wounds
CA2135646A1 (en) 1992-05-11 1993-11-25 Kenneth G. Draper Method and reagent for inhibiting viral replication
EP0786522A2 (en) 1992-07-17 1997-07-30 Ribozyme Pharmaceuticals, Inc. Enzymatic RNA molecules for treatment of stenotic conditions
US6054121A (en) * 1993-02-26 2000-04-25 The Picower Institute For Medical Research Modulation of immune responses in blood-borne mesenchymal cells
US5804446A (en) * 1993-02-26 1998-09-08 The Picower Institute For Medical Research Blood-borne mesenchymal cells
US5654186A (en) * 1993-02-26 1997-08-05 The Picower Institute For Medical Research Blood-borne mesenchymal cells
AU7043694A (en) 1993-05-27 1994-12-20 Regents Of The University Of Michigan, The Method of treatment and prevention of immune complex-induced lung injury
US5698589A (en) * 1993-06-01 1997-12-16 International Medical Innovations, Inc. Water-based topical cream containing nitroglycerin and method of preparation and use thereof
GB9317120D0 (en) * 1993-08-17 1993-09-29 Royal Postgrad Med School Human serum amyloid p component
US5981470A (en) 1994-06-07 1999-11-09 The University Of Birmingham Uterine fibroid treatment
US5989811A (en) * 1994-09-29 1999-11-23 Urocor, Inc. Sextant core biopsy predictive mechanism for non-organ confined disease status
US6030815A (en) 1995-04-11 2000-02-29 Neose Technologies, Inc. Enzymatic synthesis of oligosaccharides
US5922577A (en) 1995-04-11 1999-07-13 Cytel Corporation Enzymatic synthesis of glycosidic linkages
US5876980A (en) 1995-04-11 1999-03-02 Cytel Corporation Enzymatic synthesis of oligosaccharides
US5728554A (en) 1995-04-11 1998-03-17 Cytel Corporation Enzymatic synthesis of glycosidic linkages
CA2204743C (en) * 1995-09-13 2008-09-02 Keiji Sakamoto D-pantolactone hydrolase and gene encoding the same
US5750345A (en) 1995-10-31 1998-05-12 Evanston Hospital Corporation Detection of human α-thalassemia mutations and their use as predictors of blood-related disorders
AU712819B2 (en) 1996-01-25 1999-11-18 Profylakse Aps Pharmaceutical composition comprising serum amyloid P component for proph ylactic or therapeutic treatment of virus infections and a kit for detecting binding of compositions to virus components
ATE296315T1 (de) 1997-06-24 2005-06-15 Genentech Inc Galactosylierte glykoproteine enthaltende zusammensetzungen und verfahren zur deren herstellung
US6395713B1 (en) 1997-07-23 2002-05-28 Ribozyme Pharmaceuticals, Inc. Compositions for the delivery of negatively charged molecules
AU8525098A (en) 1997-07-24 1999-02-16 Inex Pharmaceuticals Corporation Liposomal compositions for the delivery of nucleic acid catalysts
US6365570B1 (en) * 1997-10-10 2002-04-02 Universiteit Utrecht Pharmaceutical and diagnostic use of Serum Amyloid P component
ATE419009T1 (de) 1997-10-31 2009-01-15 Genentech Inc Methoden und zusammensetzungen bestehend aus glykoprotein-glykoformen
IL137919A0 (en) * 1998-02-17 2001-10-31 Medarex Inc Treating and diagnosing macrophage-mediated diseases using fc receptor ligands
DE99907899T1 (de) 1998-03-11 2005-01-13 Kabushiki Kaisha Soken Hautnormalisierungsmittel
PT1071700E (pt) 1998-04-20 2010-04-23 Glycart Biotechnology Ag Modificação por glicosilação de anticorpos para melhorar a citotoxicidade celular dependente de anticorpos
JPH11319542A (ja) 1998-05-08 1999-11-24 Tokuyama Corp 超薄層の製造方法
US6660843B1 (en) * 1998-10-23 2003-12-09 Amgen Inc. Modified peptides as therapeutic agents
US6600019B2 (en) * 2000-01-06 2003-07-29 Curagen Corporation Polypeptides and nucleic acids encoding same
EP1267795A1 (en) 2000-03-30 2003-01-02 Brennen Medical Inc. Anti-microbial and immunostimulating composition
US20040068095A1 (en) * 2001-03-14 2004-04-08 Shimkets Richard A. Novel human proteins, polynucleotides encoding them and methods of using the same
US7713705B2 (en) * 2002-12-24 2010-05-11 Biosite, Inc. Markers for differential diagnosis and methods of use thereof
US6872541B2 (en) * 2001-07-25 2005-03-29 Coulter International Corp. Method and compositions for analysis of pentraxin receptors as indicators of disease
US6537811B1 (en) * 2001-08-01 2003-03-25 Isis Pharmaceuticals, Inc. Antisense inhibition of SAP-1 expression
US20030199442A1 (en) 2001-10-09 2003-10-23 Alsobrook John P. Therapeutic polypeptides, nucleic acids encoding same, and methods of use
JP2004049214A (ja) 2001-11-29 2004-02-19 Nippon Shokubai Co Ltd 蛋白質またはペプチドの細胞内導入方法
US7022476B2 (en) * 2002-02-26 2006-04-04 New York Society For Ruptured And Crippled Maintaining The Hospital For Special Surgery Human FcγRIIB gene polymorphisms for assessing development of systemic lupus erythematosus and compositions for use thereof
GB0211136D0 (en) 2002-05-15 2002-06-26 Univ London Treatment and prevention of tissue damage
US20050182042A1 (en) * 2002-05-17 2005-08-18 Feldman David L. Pharmaceutical composition comprising a renin inhibitor, a calcium channel blocker and a diuretic
GB0216648D0 (en) 2002-07-18 2002-08-28 Lonza Biologics Plc Method of expressing recombinant protein in CHO cells
CA2495251C (en) 2002-08-14 2018-03-06 Macrogenics, Inc. Fc.gamma.riib-specific antibodies and methods of use thereof
JP4819364B2 (ja) * 2002-12-23 2011-11-24 ウイリアム、マーシュ、ライス、ユーニヴァーサティ 線維細胞形成阻害の検出方法、ならびに線維細胞形成を増強する方法および化合物
US7763256B2 (en) * 2002-12-23 2010-07-27 William Marsh Rice University Compositions and methods for suppressing fibrocytes and for detecting fibrocyte differentiation
US8012472B2 (en) * 2002-12-23 2011-09-06 William Marsh Rice University Compositions and methods for suppressing fibrocytes
JP2006526140A (ja) 2002-12-24 2006-11-16 バイオサイト インコーポレイテッド 鑑別診断のためのマーカーおよびその使用方法
US20070149450A1 (en) 2003-02-27 2007-06-28 Ranjit Bhardwaj Method for reducing levels of c-reactive protein
MXPA06011796A (es) 2004-04-16 2007-05-07 Macrogenics Inc Anticuerpos especificos de fc(riib y metodos para el uso de los mismos.
KR101297146B1 (ko) 2004-05-10 2013-08-21 마크로제닉스, 인크. 인간화 FcγRIIB 특이적 항체 및 그의 사용 방법
WO2006002438A2 (en) 2004-06-03 2006-01-05 Medarex, Inc. Human monoclonal antibodies to fc gamma receptor i (cd64)
WO2006002930A2 (en) 2004-06-30 2006-01-12 Friedrich-Alexander- Universitaet Erlangen- Nuernberg FcϜRIIa POLYMORPHISM AND ITS USE IN DIAGNOSIS
ZA200701783B (en) 2004-09-02 2009-10-28 Genentech Inc Anti-Fc-gamma RIIB receptor antibody and uses therefor
US7553653B2 (en) * 2004-09-17 2009-06-30 Biomarin Pharmaceutical Inc. Variants and chemically-modified variants of phenylalanine ammonia-lyase
WO2006039418A2 (en) 2004-09-30 2006-04-13 Medarex, Inc. Human monoclonal antibodies to fc gamma receptor ii (cd32)
US7405302B2 (en) 2005-10-11 2008-07-29 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (FLAP) inhibitors
US20070099251A1 (en) 2005-10-17 2007-05-03 Institute For Systems Biology Tissue-and serum-derived glycoproteins and methods of their use
US20070243163A1 (en) 2006-02-17 2007-10-18 Chih-Ping Liu Respiratory tract delivery of interferon-tau
US8247370B2 (en) * 2006-12-04 2012-08-21 Promedior, Inc. Conjoint therapy for treating fibrotic diseases
US8497243B2 (en) * 2007-07-06 2013-07-30 Promedior, Inc. Methods and compositions useful in the treatment of mucositis
ES2554167T3 (es) 2007-07-06 2015-12-16 Promedior Inc. Métodos y composiciones útiles en el tratamiento de mucositis
US9884899B2 (en) 2007-07-06 2018-02-06 Promedior, Inc. Methods for treating fibrosis using CRP antagonists
JP5797565B2 (ja) * 2009-03-11 2015-10-21 プロメディオール, インコーポレイテッド 過敏性障害(hypersensitive disorder)に対する処置および診断方法
CA2755047C (en) * 2009-03-11 2018-12-04 Promedior, Inc. Treatment methods for autoimmune disorders
US20100266643A1 (en) 2009-04-01 2010-10-21 Willett W Scott Pulmonary and nasal delivery of serum amyloid p
UA110323C2 (en) 2009-06-04 2015-12-25 Promedior Inc Derivative of serum amyloid p and their receipt and application
ES2552793T3 (es) * 2009-06-17 2015-12-02 Promedior Inc. Variantes de SAP y su uso

Also Published As

Publication number Publication date
DK3042915T3 (en) 2018-11-05
HRP20181803T1 (hr) 2018-12-28
US20230058309A1 (en) 2023-02-23
CO6480917A2 (es) 2012-07-16
EA201171490A1 (ru) 2012-05-30
SI2438083T1 (sl) 2016-04-29
CA2764461C (en) 2021-05-04
EP3042915B1 (en) 2018-08-08
SI3042915T1 (sl) 2018-12-31
ES2692815T3 (es) 2018-12-05
TR201815592T4 (tr) 2018-11-21
EA030332B1 (ru) 2018-07-31
BRPI1012924B1 (pt) 2020-12-22
CN102574902A (zh) 2012-07-11
ZA201108857B (en) 2018-11-28
ES2563748T3 (es) 2016-03-16
AU2010256426A1 (en) 2012-01-12
US20100317596A1 (en) 2010-12-16
US20180044387A1 (en) 2018-02-15
UA110323C2 (en) 2015-12-25
NZ596849A (en) 2013-08-30
EP3042915A1 (en) 2016-07-13
LT3042915T (lt) 2018-11-12
JP2017082008A (ja) 2017-05-18
HK1168603A1 (zh) 2013-01-04
DK2438083T3 (en) 2016-03-07
US20210179679A1 (en) 2021-06-17
CA2764461A1 (en) 2010-12-09
BR122020010980B1 (pt) 2021-07-06
BRPI1012924A2 (pt) 2016-04-05
US20200369735A1 (en) 2020-11-26
BRPI1012924B8 (pt) 2021-05-25
JP2015120754A (ja) 2015-07-02
MY158761A (en) 2016-11-15
PT3042915T (pt) 2018-10-18
PL2438083T3 (pl) 2016-06-30
WO2010141918A1 (en) 2010-12-09
EP2438083A4 (en) 2012-11-21
CR20110640A (es) 2012-01-30
JP5801293B2 (ja) 2015-10-28
PL3042915T3 (pl) 2019-01-31
CY1120817T1 (el) 2019-12-11
IL216744A (en) 2016-09-29
WO2010141918A9 (en) 2013-03-28
HUE026737T2 (en) 2016-07-28
MX2011012738A (es) 2012-02-21
CN102574902B (zh) 2016-01-20
IL216744A0 (en) 2012-02-29
US9296800B2 (en) 2016-03-29
EP2438083B1 (en) 2015-12-02
EP2438083A1 (en) 2012-04-11
AU2010256426B2 (en) 2016-03-31
JP2012529429A (ja) 2012-11-22

Similar Documents

Publication Publication Date Title
HRP20160221T1 (hr) Serum amiloidni p derivati i njihova priprema i upotreba
US20230279048A1 (en) Compositions containing hc-ha/ptx3 complexes and methods of use thereof
Teixeira et al. Biological applications of plants and algae lectins: An overview
Ligtenberg et al. Salivary agglutinin/glycoprotein-340/DMBT1: a single molecule with variable composition and with different functions in infection, inflammation and cancer
JP5057383B2 (ja) 新規ムチン型糖タンパク質及びその用途
Sun et al. An anti-lipopolysaccharide factor from red swamp crayfish, Procambarus clarkii, exhibited antimicrobial activities in vitro and in vivo
KR101569751B1 (ko) 부분 탈아세틸화 키틴 유도체의 조성물
CN105555290B (zh) 抗微生物肽
AU2002328203B2 (en) Antimicrobial and anti-inflammatory peptides
Kamel et al. Novel anti-arthritic mechanisms of Polydatin in complete Freund’s adjuvant-induced arthritis in rats: involvement of IL-6, STAT-3, IL-17, and NF-кB
GB2477914A (en) Biofilm disruption using microbial nucleases
JP2002544759A (ja) カチオン性ペプチド単独、または抗生物質と組み合わせて用いて感染を処置するための組成物および方法
NL2011626C2 (en) Novel polypeptide and uses thereof.
AU2002328203A1 (en) Antimicrobial and anti-inflammatory peptides
KR20090027213A (ko) 개선된 항미생물성 펩타이드
Shah et al. Multifaceted applications of ulvan polysaccharides: Insights on biopharmaceutical avenues
CN107312765B (zh) 一种糖胺聚糖裂解酶及其编码基因与应用
JP4505631B2 (ja) ヘパラン硫酸糖鎖を付加したヘパリン結合性タンパク質、その製造方法及びそれを含有する医薬組成物
TWI593704B (zh) 具有抗病原菌功效的抗菌胜肽及其製藥用途
Scavello et al. The antimicrobial peptides secreted by the chromaffin cells of the adrenal medulla link the neuroendocrine and immune systems: From basic to clinical studies
Wang et al. Antibacterial peptides-loaded bioactive materials for the treatment of bone infection
Fu et al. Antibacterial, wet adhesive, and healing-promoting nanosheets for the treatment of oral ulcers
JP3903503B2 (ja) 可溶性ポリペプチド
CN110448676B (zh) 人α防御素5改造肽在制备中和内毒素药物中的应用
US8815812B2 (en) Synthetic arginine substituted peptides and their use