CA2399550A1 - Method for treating inflammatory bowel disease and other forms of gastrointestinal inflammation - Google Patents

Method for treating inflammatory bowel disease and other forms of gastrointestinal inflammation Download PDF

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Publication number
CA2399550A1
CA2399550A1 CA002399550A CA2399550A CA2399550A1 CA 2399550 A1 CA2399550 A1 CA 2399550A1 CA 002399550 A CA002399550 A CA 002399550A CA 2399550 A CA2399550 A CA 2399550A CA 2399550 A1 CA2399550 A1 CA 2399550A1
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CA
Canada
Prior art keywords
nucleic acid
subject
immunomodulatory nucleic
pyrimidine
inflammatory bowel
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Abandoned
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CA002399550A
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French (fr)
Inventor
Eyal Raz
Daniel Rachmilewitz
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Tel Aviv Sourasky Medical Center
University of California
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Individual
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088Compounds having three or more nucleosides or nucleotides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088Compounds having three or more nucleosides or nucleotides
    • A61K31/7105Natural ribonucleic acids, i.e. containing only riboses attached to adenine, guanine, cytosine or uracil and having 3'-5' phosphodiester links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088Compounds having three or more nucleosides or nucleotides
    • A61K31/711Natural deoxyribonucleic acids, i.e. containing only 2'-deoxyriboses attached to adenine, guanine, cytosine or thymine and having 3'-5' phosphodiester links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6891Pre-targeting systems involving an antibody for targeting specific cells
    • A61K47/6893Pre-targeting systems involving an antibody for targeting specific cells clearing therapy or enhanced clearance, i.e. using an antibody clearing agents in addition to T-A and D-M
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6891Pre-targeting systems involving an antibody for targeting specific cells
    • A61K47/6897Pre-targeting systems with two or three steps using antibody conjugates; Ligand-antiligand therapies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6891Pre-targeting systems involving an antibody for targeting specific cells
    • A61K47/6897Pre-targeting systems with two or three steps using antibody conjugates; Ligand-antiligand therapies
    • A61K47/6898Pre-targeting systems with two or three steps using antibody conjugates; Ligand-antiligand therapies using avidin- or biotin-conjugated antibodies
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery

Abstract

The invention provides a method for ameliorating gastrointestinal inflammation, particularly chronic gastrointestinal inflammation such as inflammatory bowel disease (IBD), in a subject. In one embodiment, the metho d comprises administering an immunomodulatory nucleic acid to a subject suffering from or susceptible to gastrointestinal inflammation.

Description

METHOD

Claims (46)

What is claimed is:
1. A method for ameliorating gastrointestinal inflammation in a subject comprising:
administering to a subject suffering from gastrointestinal inflammation a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising the sequence 5'-CpG-3', said administering being in an amount effective to ameliorate a symptom of gastrointestinal inflammation in the subject;
wherein gastrointestinal inflammation is ameliorated in the subject.
2. The method of claim 1, wherein the immunomodulatory nucleic acid comprises the sequence 5'-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3'.
3. The method of claim 1, wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of:
a) 5'-Purine-TCG-Pyrimidine-Pyrimidine-3;
b) 5'-[TCG]n3', where n is any integer that is 1 or greater;
c) 5'-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3'; and d) 5'-Purine-TCG-Pyrimidine-Pyrimidine-CG-3'
4. The method of claim 1, wherein the immunomodulatory nucleic acid molecule is selected from the group consisting of an immunostimulatory oligodeoxyribonucleotide (ISS-ODN); an isolated bacterial genomic DNA and plasmid DNA comprising an immunomodulatory nucleic acid sequence.
5. The method of claim 1, wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.
6. The method of claim 4, wherein the immunomodulatory nucleic acid molecule comprises at least one sequence selected from the group consisting of AACGTT, aacgttcg, aacgtt, gtcgtt, and tcgtcg.
7. The method of claim 4, wherein the immunomodulatory nucleic acid molecule comprises at least one sequence selected from the group consisting of tgactgtgaacgttcgagatga (SEQ ID NO:1), tgactgtgaacgttagagatga (SEQ ID NO:5), tgactgtggtcgttagagatga (SEQ ID NO:9), tcgtcgtcgtcgtcgtcgtcgt (SEQ ID NO:10), and tgaaacgttcgcctgtcgttga (SEQ ID NO:11).
8. The method of claim 1, wherein the immunomodulatory nucleic acid is administered via a gastroenteral route.
9. The method of claim 1, wherein the gastroenteral route is oral, intranasal, intragastric or rectal
10. The method of claim 1, wherein the immunomodulatory nucleic acid is administered by a systemic route.
11. The method of claim 10, wherein the systemic route is intradermal, intramuscular, subcutaneous or intravenous.
12. The method of claim 1, wherein the immunomodulatory nucleic acid is administered by a mucosal route.
13. The method of claim 1, wherein the gastrointestinal inflammation is chronic gastrointestinal inflammation.
14. The method of claim 13, wherein the chronic gastrointestinal inflammation is caused by inflammatory bowel disease.
15. The method of claim 14, wherein the inflammatory bowel disease is ulcerative colitis.
16. The method of claim 14, wherein the inflammatory bowel disease is Crohn's disease.
17. The method of claim 14, wherein the immunomodulatory nucleic acid is administered in conjunction with a steroid or an antibody directed against tumor necrosis factor-.alpha. (TNF-.alpha.).
18. The method of claim 1, wherein the gastrointestinal inflammation is acute gastrointestinal inflammation.
19. A method for ameliorating inflammatory bowel disease in a subject comprising:
administering to a subject suffering from inflammatory bowel disease a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising the sequence 5'-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3', said administering being in an amount effective to ameliorate a symptom of inflammatory bowel disease in the subject;
wherein inflammatory bowel disease is ameliorated in the subject.
20. The method of claim 19, wherein said administering is by an intragastric route.
21. The method of claim 19, wherein said administering is by a subcutaneous route.
22. A method for ameliorating inflammatory bowel disease in a subject comprising:
administering to a subject suffering from inflammatory bowel disease a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising at least one sequence selected from the group consisting of tgactgtgaacgttcgagatga (SEQ ID NO:1), tgactgtgaacgttagagatga (SEQ ID NO:5), tgactgtggtcgttagagatga (SEQ ID NO:9), tcgtcgtcgtcgtcgtcgtcgt (SEA ID NO:10), and tgaaacgttcgcctgtcgttga (SEQ m NO:11), said administering being in an amount effective to ameliorate a symptom of inflammatory bowel disease in the subject;
23. A method for reducing inflammation caused by a gastrointestinal inflammatory disease in a subject, the method comprising:
administering to a subject suffering from gastrointestinal inflammatory disease a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising the sequence 5'-CpG-3', said administering being in an amount effective to reduce inflammation caused by gastrointestinal inflammatory disease in the subject;
wherein inflammation caused by gastrointestinal inflammatory disease is reduced in the subject.
24. The method of claim 23, wherein the immunomodulatory nucleic acid comprises the sequence 5'-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3'.
25. The method of claim 23, wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of:
a) 5'-Purine-TCG-Pyrimidine-Pyrimidine-3 ;
b) 5'-[TCG]n-3', where n is any integer that is 1 or greater;
c) 5'-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3'; and d) 5'-Purine-TCG-Pyrimidine-Pyrimidine-CG-3'
26. The method of claim 23, wherein the immunomodulatory nucleic acid molecule is selected from the group consisting of an immunostimulatory oligodeoxyribonucleotide (ISS-ODN); an isolated, detoxified bacterial polynucleotide; bacterial genomic DNA;
and a plasmid DNA comprising an immunomodulatory nucleic acid.
27. The method of claim 23, wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.
28. The method of claim 23, wherein the immunomodulatory nucleic acid molecule comprises the sequence at least one sequence selected from the group consisting of aacgtt, aacgttcg, aacgtt, gtcgtt, and tcgtcg.
29. The method of claim 23, wherein the immunomodulatory nucleic acid comprises at least one sequence selected from the group consisting of tgactgtgaacgttcgagatga (SEQ ID
NO:1), tgactgtgaacgttagagatga (SEQ ID NO:5), tgactgtggtcgttagagatga (SEQ ID
NO:9), tcgtcgtcgtcgtcgtcgtcgt (SEQ ID NO: 10), and tgaaacgttcgcctgtcgttga (SEQ ID
NO:11).
30. The method of claim 23, wherein the immunomodulatory nucleic acid is administered via a gastroenteral route.
31. The method of claim 30, wherein the gastroenteral route is oral, intranasal, intragastric or rectal.
32. The method of claim 23, wherein the immunomodulatory nucleic acid is administered by a systemic route.
33. The method of claim 32, wherein the systemic route is intradermal, intramuscular, subcutaneous or intravenous.
34. The method of claim 23 wherein the immunomodulatory nucleic acid is administered by a mucosal route.
35. The method of claim 23, wherein the gastrointestinal inflammation is chronic gastrointestinal inflammation.
36. The method of claim 33, wherein the chronic gastrointestinal inflammation is caused by inflammatory bowel disease.
37. The method of claim 36, wherein the immunomodulatory nucleic acid is administered in conjunction with a steroid or an antibody directed against tumor necrosis factor-.alpha. (TNF-.alpha.).
38. The method of claim 35, wherein the chronic gastrointestinal inflammatory disease is ulcerative colitis.
39. The method of claim 35, wherein the chronic gastrointestinal inflammatory disease is Crohn's disease.
40. A method for reducing inflammation caused by inflammatory bowel disease in a subject comprising:
administering to a subject suffering from inflammatory bowel disease a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising the sequence 5'-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3', said administering being in an amount effective to reduce inflammation caused by inflammatory bowel disease in the subject;
wherein inflammation caused by inflammatory bowel disease is reduced in the subject.
41. The method of claim 40, wherein said administering is by an intragastric route.
42. The method of claim 40, wherein said administering is by a subcutaneous route.
43. The method of claim 40, wherein the inflammatory bowel disease is ulcerative colitis.
44. The method of claim 40, wherein reduction of inflammation of ulcerative colitis further decreases the risk of colonic carcinoma.
45. The method of claim 43, wherein the inflammatory bowel disease is Crohn's disease.
46. A method for reducing inflammation of inflammatory bowel disease in a subject comprising:
administering to a subject suffering from inflammatory bowel disease a formulation comprising an immunomodulatory nucleic acid to the subject, the immunomodulatory nucleic acid comprising at least one sequence selected from the group consisting of tgactgtgaacgttcgagatga (SEQ ID NO:1), tgactgtgaacgttagagatga (SEQ ID NO:5), tgactgtggtcgttagagatga (SEQ ID NO:9), tcgtcgtcgtcgtcgtcgtcgt (SEQ ID NO:10), and tgaaacgttcgcctgtcgttga (SEQ ID NO:11), said administering being in an amount effective to reduce inflammation in the subject;
wherein inflammation caused by inflammatory bowel disease is reduced in the subject.
CA002399550A 2000-02-23 2001-02-22 Method for treating inflammatory bowel disease and other forms of gastrointestinal inflammation Abandoned CA2399550A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US18425600P 2000-02-23 2000-02-23
US60/184,256 2000-02-23
PCT/US2001/006034 WO2001062207A2 (en) 2000-02-23 2001-02-22 Method for treating inflammatory bowel disease and other forms of gastrointestinal inflammation

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CA2399550A1 true CA2399550A1 (en) 2001-08-30

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US (2) US6613751B2 (en)
EP (1) EP1259264A4 (en)
AU (3) AU2001241751B2 (en)
CA (1) CA2399550A1 (en)
IL (1) IL151345A0 (en)
WO (1) WO2001062207A2 (en)

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