US2014356332A1PendingUtilityA1

Enhancing vessel lesion homing and repair potential of stem cells

50
Assignee: UNIV FLORIDAPriority: Mar 20, 2008Filed: May 7, 2014Published: Dec 4, 2014
Est. expiryMar 20, 2028(~1.7 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 9/10A61K 35/28C12N 2310/3233C12N 2310/11C12N 5/0647C12N 15/1136C12N 2320/31A61K 2035/124C12N 2501/15C12N 2310/14C12N 2320/32
50
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

Disclosed herein are methods of enhancing repair of vascular lesions involving the administration of cells in which TGF-β expression and/or activity has been transiently blocked. Other methods involve the administration of a TGF-β blocking agent to a subject who has a vascular lesion or is at risk of developing a vascular lesion. Alternatively, a TGF-β blocking agent and treated cells are co-administered to a subject in need thereof.

Claims

exact text as granted — not AI-modified
1 - 16 . (canceled) 
     
     
         17 . A method of diminishing diabetic retinopathy in a subject comprising administering to said subject CD34+ cells treated, ex vivo, with a TGF-β1 blocking agent under conditions to enhance homing ability of said CD34+ cells. 
     
     
         18 . The method of  claim 17 , wherein said administering comprises parenterally or intraoptically injecting cells. 
     
     
         19 . A method of enhancing repair of vessel lesion in a subject comprising administering to said subject CD34+ cells treated with a TGF-β1 blocking agent under conditions to enhance homing ability of said CD34+ cells. 
     
     
         20 . The method of  claim 19 , wherein said administering comprises parenterally injecting cells. 
     
     
         21 . The method of  claim 19 , wherein said CD34+ cells are autologous or allogeneic in origin. 
     
     
         22 . (canceled) 
     
     
         23 . (canceled) 
     
     
         24 . A method of treating a condition in a patient in need thereof, said method comprising administering to said patient a therapeutically effective amount of a TGF-β1 blocking agent, and, optionally, co-administering stem cells subjected, ex vivo, to a TGF-β1 blocking agent, wherein said condition is a vessel lesion. 
     
     
         25 . The method of  claim 24 , wherein said condition is a stroke. 
     
     
         26 . The method of  claim 24 , wherein said condition is a myocardial infarction. 
     
     
         27 . The method of  claim 24 , wherein said condition is choroidal neovascularization. 
     
     
         28 . The method of  claim 24 , wherein said condition is diabetes. 
     
     
         29 . The method of  claim 24 , wherein said condition is nephropathy. 
     
     
         30 . The method of  claim 24 , wherein said administering comprises intraocular delivery. 
     
     
         31 . The method of  claim 24 , wherein said intraocular delivery comprises intravitreal injection. 
     
     
         32 . (canceled) 
     
     
         33 . (canceled) 
     
     
         34 . (canceled) 
     
     
         35 . (canceled) 
     
     
         36 . (canceled) 
     
     
         37 . (canceled) 
     
     
         38 . (canceled) 
     
     
         39 . A lesion treating composition comprising treated CD34+ cells, said treated CD34+ cells obtained by procuring CD34+ cells from a subject and treating said procured CD34+ cells, ex vivo, by blocking activity of TGF-β1 under conditions to enhance homing ability of said CD34+ cells. 
     
     
         40 . An isolated, enriched population of CD34+ stem cells comprising an effective amount of an exogenous antisense oligonucleotide that blocks endogenous TGF-β1.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.