Interleukin 10

• US 20030186386A1
• Filed: 12/03/2002
• Published: 10/02/2003
• Est. Priority Date: 02/11/2000
• Status: Abandoned Application

• Current Assignee: Perseid Therapeutics LLC (Astellas Pharma Incorporated)
• Original Assignee: Perseid Therapeutics LLC (Astellas Pharma Incorporated)
• Inventors: Hansen, Christian Karsten, Andersen, Kim Vilbour
• Application Number:
  US10/203,531
• Publication Number:
  US 20030186386A1
• Time in Patent Office: Days
• US Class Current: 435/69.52
• CPC Class Codes: A61K 38/00 Medicinal preparations containing peptides peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00
• CPC Class Codes: A61K 47/60 the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
• CPC Class Codes: C07K 14/5428 IL-10

Abstract

Conjugates exhibiting IL-10 activity comprising (i) a polypeptide which comprises an amino acid sequence that differs from that of human IL-10 in at least one amino acid residue selected from an introduced or removed amino acid residue comprising an attachment group for the non-polypeptide moiety of (ii), and (ii) a non-polypeptide moiety. The conjugates have increased half-life as compared to hIL-10 and may be used for treatment of, e.g., inflammatory diseases.

Claims

1. A conjugate exhibiting IL-10 activity comprising

i) a polypeptide which comprises an amino acid sequence that differs from the amino acid sequence shown in SEQ ID NO 2 in at least one amino acid residue selected from an introduced or removed amino acid residue comprising an attachment group for the non-polypeptide moiety of ii), and ii) a non-polypeptide moiety.

2. The conjugate according to claim 1, comprising 1-10 non-polypeptide moieties.

3. The conjugate according to claim 1 or 2, wherein the polypeptide i) exhibits IL-10 activity.

4. The conjugate according to any of claims 1-3, wherein said polypeptide comprises an amino acid sequence that differs from the amino acid sequence shown in SEQ ID NO 2 in the introduction of at least one lysine residue in a position selected from the group consisting of S1, P2, G3, Q4, G5, T6, Q7, S8, E9, N10, S11, T13, H14, P16, G17, N18, P20, N21, R24, D25, R27, D28, S31, R32, T35, Q38, M39, Q42, L43, D44, N45, L46, E50, S51, E54, G58, S66, Q70, E74, E75, P78, Q79, N82, Q83, D84, P85, D86, A89, H90, N92, S93, E96, N97, T100, R102, L103, R106, R107, H109, R110, P113, E122, Q123, N126, A127, N129, Q132, E133, D144, I145, N148, E151, T155, M156, R159, and N160.

5. A conjugate according to any of claims 14, wherein said polypeptide comprises an amino acid sequence that differs from the amino acid sequence shown in SEQ ID NO 2 in at least one substitution selected from the group consisting of K34X, K40X, K49X, K57X, K88X, K99X, K117X, K119X, K125X, K130X, K134X, K138X and K157X, wherein X is any amino acid residue except K and preferably is R.

6. The conjugate according to any of claims 1-5, wherein two or more residues present in SEQ ID NO 2 have been substituted with any other amino acid residue.

7. The conjugate according to any of claims 1-6, wherein the non-polypeptide moiety is a polymer molecule, e.g. PEG.

8. The conjugate according to any of claims 1-7, wherein the polypeptide is glycosylated.

9. The conjugate according to any of claims 1-8, wherein at least one glycosylation site has been introduced.

10. A conjugate according to any of claims 1-9, wherein said polypeptide comprises an amino acid sequence that differs from the amino acid sequence shown in SEQ ID NO 2 in at least one substitution selected from the group consisting of P2N+Q4S, P2N+Q4T, G3N+G5S, G3N+G5T, Q4N+T6S, Q4N, G5N+Q7S, G5N+Q7T, T6N, T6N+S8T, Q7N+E9S, Q7N+E9T, S8N+N10S, S8N+N10T, E9N, E9N+S11T, S11N+T13S, S11N, H14N+P16S, H14N+P16T, P16N+N18S, P16N+N18T, P20S, P20T, P20N+M22S, 5 P20N+M22T, L23S, L23T, R24N+L26S, R24N+L26T, D25N+R27S, D25N+R27T, R27N+A29S, R27N+A29T, D28N+F30S, D28N+F30T, S31N+V33S, S31N+V33T, R32N+K34S, R32N+K34T, K34N+F36S, K34N+F36T, T35N+F37S, T35N+F37T, Q38N+K40S, Q38N+K40T, M39N+D41S, M39N+D41T, K40N+Q42S, K40N+Q42T, Q42N+D44S, Q42N+D44T, L43N+N45S, L43N+N45T, D44N+L46S, D44N+L46T, L47S, L47T, L46N+L48S, L46N+L48T, K49N, K49N+S51T, E50N+L52S, E50N+L52T, S51N+L53S, S51N+L53T, E54N+F56S, E54N+F56T, K57N+Y59S, K57N+Y59T, G58N+L60S, G58N+L60T, S66N+M68S, S66N+M68T, Q70N+Y72S, Q70N+Y72T, E74N+V76S, E74N+V76T, P78N+A80S, P78N+A80T, Q79N+E81S, Q79N+E81T, Q83N+P85S, Q83N+P85T, P85N+187S, P85N+187T, D86N+K88S, D86N+K88T, K88N+H90S, K88N+H90T, A89N+V91S, A89N+V91T, H90N+N92S, H90N+N92T, L94S, L94T, S93N+G95S, S93N+G95T, E96N+L98S, E96N+L98T, K99S, K99T, K99N+L101S, K99N+L101T, T100SN+R102S, T100N+R102T, R102N+R104S, R102N+R104T, L103N+L 105S, L103N+L105T, R107N+H109S, R107N+H109T, H109N+F111S, H109N+F111T, P113N+E115S, P113N+E115T, K117N+K119S, K117N+K119T, E122N+V124S, E122N+V124T, Q123N+K125S, Q123N+K125T, K125N+A127S, K125N+A127T, F128S, F128T, A127N+N129S, A127N+N129T, L131S, L131T, K130N+Q132S, K130N+Q132T, Q132N+K134S, Q132N+K134T, E133N+G135S, E133N+G135T, K134N+I136S, K134N+I136T, D144N+F146S, D144N+F146T, I145N+I147S, I145N+I147T, I150S, I150T, E151N+Y153S, E151N+Y153T, T155N+K157S, T155N+K157T, M156N+I158S, M156N+I158T, K157N+R159S and K157N+R159T.

11. A conjugate according to any of claims 1-10, wherein said polypeptide comprises an amino acid sequence that differs from the amino acid sequence shown in SEQ ID NO 2 in the removal, preferably by substitution, of at least one of the amino acid residues selected from the group consisting of N116 and S118.

12. The conjugate according to any of claims 1-11, which is glycosylated and PEGylated.

13. The conjugate according to any of the preceding claims, which has a reduced susceptibility to renal clearance as compared to hIL-10.

14. The conjugate according to any of the preceding claims, which has an increased functional in vivo half-life and/or serum half-life as compared to hIL-10.

15. A substantially homogeneous preparation of a conjugate according to any of claims 1-14.

16. A polypeptide exhibiting IL-10 activity, which has the amino acid sequence of the polypeptide i) defined in any of claims 1-11.

17. A nucleotide sequence encoding a polypeptide according to claim 16.

18. An expression vector harbouring a nucleotide sequence according to claim 17.

19. A host cell comprising a nucleotide sequence according to claim 17 or an expression vector according to claim 18.

20. A method of producing a polypeptide exhibiting IL-10 activity, which method comprises subjecting the cell according to claim 19 to cultivation under conditions conducive for the expression of the polypeptide, and optionally recovering the polypeptide.

21. The method according to claim 20, which further comprises subjecting the polypeptide to conjugation to a non-polypeptide moiety.

22. A method of increasing the functional in vivo half-life and/or serum half-life of a polypeptide exhibiting IL-10 activity, which method comprises introducing an amino acid residue change as defined in any of claims 1-11 and subjecting the resulting modified polypeptide to conjugation with the appropriate non-polypeptide moiety.

23. A method for preparing a conjugate according to any of claims 1-14, wherein the polypeptide i) is allowed to react with the non-polypeptide moiety ii) under conditions conducive for the conjugation to take place, and the resulting conjugate is recovered.

24. The method according to any of claims 21-23, wherein the conjugation to the non-polypeptide moiety is conducted in the presence of a molar excess of the non-polypeptide moiety whereby a substantially homogenous conjugate preparation is obtained.

25. A pharmaceutical composition comprising a) a conjugate according to any of claims 1-14 or a preparation according to claim 15 and b) a pharmaceutically acceptable diluent, carrier or adjuvant.

26. A conjugate according to any of claims 1-14, a preparation according to claim 15, or a composition according to claim 25 for use in the treatment of diseases, in particular treatment of inflammatory diseases, such as rheumatoid arthritis, and in connection with transplantation, immunodeficiencies and parasitic infections.

27. Use of a conjugate according to any of claims 1-14, a preparation according to claim 15, or a composition according to claim 25 for the treatment of diseases, in particular treatment of inflammatory diseases, such as rheumatoid arthritis, and in connection with transplantation, immunodeficiencies and parasitic infections.

28. Use of a conjugate according to any of claims 1-14, a preparation according to claim 15, or a composition according to claim 25 for the manufacture of a medicament for treatment of diseases, in particular treatment of inflammatory diseases, such as rheumatoid arthritis, and in connection with transplantation, immunodeficiencies and parasitic infections.

29. A method of treating a mammal having an inflammatory diseases, such as rheumatoid arthritis, and in connection with transplantation, immunodeficiencies and parasitic infections, comprising administering to a mammal in need thereof an effective amount of a conjugate according to any of claims 1-14, a preparation according to claim 15, or a composition according to claim 25.