US2007010546A1PendingUtilityA1

Method for enhancing epithelial cell proliferation and uses thereof

Individually held — no corporate assignee on recordPriority: Nov 8, 2002Filed: Jun 21, 2006Published: Jan 11, 2007
Est. expiryNov 8, 2022(expired)· nominal 20-yr term from priority
Inventors:David Weinstein
A61K 38/13
64
PatentIndex Score
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Claims

Abstract

The present invention is directed to uses of GM-284 for enhancing epithelial cell proliferation. The present invention is also provides methods for treating a keratinocyte-associated disorder in a subject in need of treatment.

Claims

exact text as granted — not AI-modified
1 . A method for enhancing epithelial cell proliferation, comprising contacting epithelial tissue with an amount of an immunophilin ligand effective to enhance epithelial cell proliferation.  
   
   
       2 . The method of  claim 1 , wherein the epithelial cell is selected from the group consisting of a glandular cell, a Langerhans cell, a neural cell, and a skin cell.  
   
   
       3 . The method of  claim 2 , wherein the skin cell is a keratinocyte.  
   
   
       4 . The method of  claim 1 , wherein the immunophilin ligand is FK506 or an FK506 derivative.  
   
   
       5 . The method of  claim 4 , wherein the FK506 derivative is nonimmunosuppressive.  
   
   
       6 . The method of  claim 5 , wherein the nonimmunosuppressive FK506 derivative is GM-284.  
   
   
       7 . The method of  claim 1 , wherein the contacting is effected in vitro.  
   
   
       8 . The method of  claim 1 , wherein the contacting is effected in vivo in a subject.  
   
   
       9 . The method of  claim 8 , wherein the enhanced epithelial cell proliferation promotes healing of a wound in the subject.  
   
   
       10 . The method of  claim 8 , wherein the contacting is effected in vivo in a subject by administering the immunophilin ligand to the subject.  
   
   
       11 . The method of  claim 10 , wherein the immunophilin ligand is administered to the subject by oral administration, parenteral administration, sublingual administration, topical administration, transdermal administration, or osmotic pump.  
   
   
       12 . The method of  claim 10 , wherein the subject is a human.  
   
   
       13 . The method of  claim 12 , wherein the human has a keratinocyte-associated disorder.  
   
   
       14 . The method of  claim 13 , wherein the keratinocyte-associated disorder is characterized by a dysregulation of keratinocyte proliferation.  
   
   
       15 . The method of  claim 13 , wherein the keratinocyte-associated disorder is selected from the group consisting of leprosy, periodontal disease, a peripheral neuropathy, a pressure ulcer, psoriasis, a skin ulceration, a venous stasis ulcer, and a wound.  
   
   
       16 . The method of  claim 10 , wherein the amount of the immunophilin ligand is between about 0.1 pM and about 5 mM.  
   
   
       17 . The method of  claim 16 , wherein the amount of the immunophilin ligand is between about 5 pM and about 1.5 mM.  
   
   
       18 . A method for treating a keratinocyte-associated disorder in a subject in need of treatment, comprising administering to the subject an amount of an immunophilin.

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