US2002052483A1PendingUtilityA1
Intestinal trefoil proteins
Assignee: GEN HOSPITAL CORP MASSACHUSETTPriority: Feb 14, 1991Filed: Mar 16, 2001Published: May 2, 2002
Est. expiryFeb 14, 2011(expired)· nominal 20-yr term from priority
Inventors:Daniel Podolsky
A61P 43/00A61P 35/02A61P 27/02A61P 29/00A61P 25/08A61P 35/00A61P 27/00A61P 31/04C07K 16/26A61P 17/02A61P 11/00A61K 38/00A61P 15/00C07K 14/575A61P 11/04A61P 1/00A61P 13/02A61P 1/04A61P 11/02A61P 17/00A61P 1/02A61P 1/06
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Claims
Abstract
Intestinal trefoil factors and nucleic acids encoding intestinal trefoil factors are disclosed. The intestinal trefoil factors disclosed are resistent to destruction in the digestive tract and can be used for the treatment of peptic ulcer diseases, inflammatory bowel diseases and other insults.
Claims
exact text as granted — not AI-modified1 . A purified nucleic acid encoding an intestinal trefoil factor.
2 . The purified nucleic acid of claim 1 wherein said intestinal trefoil factor is mammalian intestinal trefoil factor.
3 . The purified nucleic acid of claim 2 wherein said mammal is a human.
4 . The purified nucleic acid of claim 2 wherein said mammal is a rat.
5 . The purified nucleic acid of claim 2 wherein said mammal comprises a cow, or a pig.
6 . The purified nucleic acid of claim 1 , said purified nucleic acid being present within a vector.
7 . A cell comprising a vector encoding an intestinal trefoil factor.
8 . A substantially pure intestinal trefoil factor.
9 . A therapeutic composition comprising said factor of claim 8 and a pharmacologically acceptable carrier.
10 . A monoclonal antibody which preferentially binds the factor of claim 8 .
11 . The monoclonal antibody of claim 10 wherein said monoclonal antibody is detectably labelled.
12 . A method for detecting intestinal trefoil factor in a human patient comprising
contacting a biological sample obtained from said patient with said monoclonal antibody of claim 10 , and detecting immune complexes formed with said monoclonal antibody.
13 . The method of claim 12 wherein said biological sample is an intestinal mucosal scraping.
14 . The method of claim 12 wherein said biological sample is serum.
15 . A method for treating digestive disorders in a human patient, comprising
administering to said patient the therapeutic composition of claim 9 .
16 . The factor of claim 8 wherein said factor is detectably labelled.
17 . A method for detecting binding sites for intestinal trefoil factor in a patient comprising
contacting a biological sample obtained from said patient with said factor of claim 8 , and detecting said factor bound to said biological sample as an indication of the presence of said binding sites in said sample.
18 . An isolated DNA comprising a sequence encoding an intestinal trefoil factor.
19 . The isolated DNA of claim 18 , wherein said DNA is present within a vector.
20 . The isolated DNA of claim 18 , wherein said intestinal trefoil factor is a mammalian intestinal trefoil factor.
21 . The isolated DNA of claim 20 , wherein said mammal is a human.
22 . The isolated DNA of claim 20 , wherein said mammal is a rat.
23 . The isolated DNA of claim 20 , wherein said mammal comprises a cow, or a pig.
24 . A method for the treatment of lesions in the alimentary canal of a patient, said method comprising administering to said patient at least one trefoil peptide, or a biologically active fragment thereof.
25 . The method of claim 24 , wherein said lesion is in the mucosa of the alimentary canal.
26 . The method of claim 24 , wherein said lesion is in the mouth of the patient.
27 . The method of claim 24 , wherein said lesion is in the esophagus of the patient.
28 . The method of claim 24 , wherein said lesion is in the stomach of the patient.
29 . The method of claim 24 , wherein said lesion is in the intestine of the patient.
30 . The method of claim 24 , wherein said patient is recieving radiation therapy for the treatment of cancer.
31 . The method of claim 24 , wherein said patient is recieving chemotherapy for the treatment of cancer.
32 . The method of claim 24 , wherein said patient is recieving a drug that damages said alimentary canal.
33 . The method of claim 24 , wherein said patient is suffering from a digestive disorder.
34 . The method of claim 33 , wherein said digestive disorder is non-ulcer dispepsia.
35 . The method of claim 33 , wherein said digestive disorder is gastritis.
36 . The method of claim 33 , wherein said digestive disorder is gastro-esophageal reflux disease.
37 . The method of claim 33 , wherein said digestive disorder is a peptic ulcer or duodenal ulcer.
38 . The method of claim 24 , wherein said trefoil protein is a human trefoil protein.
39 . The method of claim 38 , wherein said trefoil peptide is intestinal trefoil peptide (ITF).
40 . The method of claim 38 , wherein said trefoil peptide is spasmolytic peptide (SP).
41 . The method of claim 38 , wherein said trefoil peptide is pS2.
42 . The method of claim 24 , wherein said administration is oral.
43 . The method of claim 24 , wherein said administration further comprises administration of mucin glycoprotein preparations.Join the waitlist — get patent alerts
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