WO2005058358B1 - Use of agents derived from ceacam1 for the treatment of inflammatory diseases - Google Patents

Use of agents derived from ceacam1 for the treatment of inflammatory diseases

Info

Publication number
WO2005058358B1
WO2005058358B1 PCT/EP2004/014435 EP2004014435W WO2005058358B1 WO 2005058358 B1 WO2005058358 B1 WO 2005058358B1 EP 2004014435 W EP2004014435 W EP 2004014435W WO 2005058358 B1 WO2005058358 B1 WO 2005058358B1
Authority
WO
WIPO (PCT)
Prior art keywords
fragment
immunoglobulin
biliary glycoprotein
fusion protein
ceacaml
Prior art date
Application number
PCT/EP2004/014435
Other languages
French (fr)
Other versions
WO2005058358A3 (en
WO2005058358A2 (en
Filing date
Publication date
Application filed filed Critical
Priority to EP04804036A priority Critical patent/EP1701739A2/en
Priority to US10/583,291 priority patent/US20080026980A1/en
Publication of WO2005058358A2 publication Critical patent/WO2005058358A2/en
Publication of WO2005058358A3 publication Critical patent/WO2005058358A3/en
Publication of WO2005058358B1 publication Critical patent/WO2005058358B1/en
Priority to US12/806,002 priority patent/US20110189181A1/en

Links

Abstract

The use of an agent that selectively modulates cross-linking of biliary glycoprotein polypeptides for the preparation of a pharmaceutical composition for preventing or treatment of a mammal subject afflicted with an inflammatory disease is provided. In particular, a method for preventing or treatment of a mammal subject afflicted with rheumatoid arthritis or multiple sclerosis, comprising the step of administering to a mammal in need thereof a therapeutic effective amount of a fusion protein of a fragment of biliary glycoprotein and a fragment of an immunoglobulin is described.

Claims

25AMENDED CLAIMS[Received by the International Bureau on 15 November 2005 (15.11.05): Original claims 1- 20 replaced by amended claims 1-22]
1. Use of an agent that selectively modulates cross-linking of biliary glycoprotein polypeptides for the preparation of a pharmaceutical composition for preventing or treatment of a mammal subject afflicted with an inflammatory disease.
2. The use of claim 1, wherein said inflammatory disease is arthritis or multiple sclerosis (MS).
3. The use of claim 2, wherein said inflammatory disease is rheumatoid arthritis (RA).
4. The use of any one of claims 1 to 3, wherein the agent is an antibody.
5. The use of claim 4, wherein the antibody is a monoclonal antibody.
6. The use of any one of claims 1 to 3, wherein the agent comprises a ligand for the biliary glycoprotein polypeptide, wherein the ligand binds at least one biliary glycoprotein polypeptides.
7. The use of claim 6, wherein the ligand is fused to an immunoglobulin molecule or a fragment thereof.
8. The use of claim 6 or 7, wherein the ligand comprises a biliary glycoprotein polypeptide or fragment thereof.
9. The use of any one of claims 6 to 8, wherein said biliary glycoprotein is a human biliary glycoprotein (CEACAMl) or a fragment thereof.
10. The use of claim 9, wherein said fragment is derived from the extracellular domain of CEACAMl.
11. The use of any one of claims 7 to 10, wherein said immunoglobulin is a human immunoglobulin or a fragment thereof.
12. The use of claim 11, wherein said immunoglobulin fragment of the immunoglobulin is the Fc portion of the immunoglobulin.
13. The use of any one of claims 9 to 12, wherein said biliary glycoprotein fragment comprises the amino sequence from position 1 to 228 of SEQ ID NO: 2 (Figure 1) or a fragment thereof and/or the immunoglobulin fragment comprises the hinge-CH2-CH3 region of the Fc portion of the immunoglobulin.
14. The use of any one of claims 1 to 13, wherein the dosage is in the range of 0.1 mg/kg/day to 25 mg/kg/day.
15. The use of any one of claims 1 to 14, wherein the pharmaceutical composition is adapted in a form to be administered intravenously, subcutaneous, intramuscular or by inhalation.
16. A fusion protein comprising a human biliary glycoprotein (CEACAMl) fragment which is derived from the extracellular domain of CEACAMl and an Fc portion of a human immunoglobulin.
17. The fusion protein of claim 16, wherein said CEACAMl fragment substantially consists of the amino sequence from position 1 to 228 of SEQ ID NO: 2 (Figure 1) or a fragment thereof.
18. A polynucleotide encoding the fusion protein of claim 16 or 17.
19. A vector comprising the polynucleotide of claim 18.
20. A host cell comprising a polynucleotide of claim 18 or a vector of claim 19.
21. A composition comprising the fusion protein of claim 16 or 17, the polynucleotide of claim 18, the vector of claim 19 or the cell of claim 20, optionally in combination with a pharmaceutically acceptable carrier. 27
22. A method for preventing or treatment of a mammal subject afflicted with rheumatoid arthritis or multiple sclerosis, comprising the step of administering to a mammal in need thereof a therapeutic effective amount of a fusion protein of a fragment of biliary glycoprotein and a fragment of an immunoglobulin.
PCT/EP2004/014435 2003-12-17 2004-12-17 Use of agents derived from ceacam1 for the treatment of inflammatory diseases WO2005058358A2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP04804036A EP1701739A2 (en) 2003-12-17 2004-12-17 Use of agents derived from ceacam1 for the treatment of inflammatory diseases
US10/583,291 US20080026980A1 (en) 2003-12-17 2004-12-17 Use of Agents Derived from Ceacam1 for the Treatment of Inflammatory Diseases
US12/806,002 US20110189181A1 (en) 2003-12-17 2010-08-02 Use of agents derived from CEACAM1 for the treatment of inflammatory diseases

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP03028968.0 2003-12-17
EP03028968 2003-12-17

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/806,002 Continuation US20110189181A1 (en) 2003-12-17 2010-08-02 Use of agents derived from CEACAM1 for the treatment of inflammatory diseases

Publications (3)

Publication Number Publication Date
WO2005058358A2 WO2005058358A2 (en) 2005-06-30
WO2005058358A3 WO2005058358A3 (en) 2005-11-24
WO2005058358B1 true WO2005058358B1 (en) 2006-01-26

Family

ID=34684544

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2004/014435 WO2005058358A2 (en) 2003-12-17 2004-12-17 Use of agents derived from ceacam1 for the treatment of inflammatory diseases

Country Status (3)

Country Link
US (2) US20080026980A1 (en)
EP (1) EP1701739A2 (en)
WO (1) WO2005058358A2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003054019A2 (en) 2001-12-21 2003-07-03 Genpat77 Pharmacogenetics Ag Therapeutic monoclonal anti-tirc7 antibodies for use in immune related and other diseases
KR101050298B1 (en) * 2008-12-03 2011-07-19 삼성에스디아이 주식회사 Secondary battery
US9556271B2 (en) 2011-12-01 2017-01-31 The Brigham And Women's Hospital, Inc. Anti-CEACAM1 recombinant antibodies for cancer therapy
CA2916638C (en) 2012-07-31 2021-01-12 The Brigham And Women's Hospital, Inc. Modulation of the immune response
WO2016120331A1 (en) 2015-01-28 2016-08-04 Karl Sebastian Lang Agonistic anti-cd66cd66 antibody for antiviral therapy

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2328725A1 (en) * 1998-04-15 1999-10-21 Brigham & Women's Hospital, Inc. T cell inhibitory receptor compositions and uses thereof

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