US2014294726A1PendingUtilityA1

Methods for diagnosing and treating alzheimer's disease by administering an anti-angiogenic agent

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Assignee: JEFFERIES WILFREDPriority: Jul 19, 2011Filed: Jul 18, 2012Published: Oct 2, 2014
Est. expiryJul 19, 2031(~5 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 25/28A61K 31/436A61K 38/208A61K 38/1709C07K 16/22A61K 38/212C07K 16/18A61K 2039/575A61K 38/484A61K 31/42A61K 38/195A61K 45/00A61K 39/0007A61K 31/44A61K 31/551A61K 31/506A61K 31/404G01N 33/5058A61K 38/21A61K 39/395A61K 2039/55566A61K 38/39A61K 31/05A61K 31/192
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Claims

Abstract

Methods for diagnosing and treating Alzheimer's disease are provided. In particular, methods of restoring blood-brain barrier integrity and/or promoting vascular reversion in a person suffering from Alzheimer's disease by administering an anti-angiogenic agent or an agent that is capable of restoring tight junction integrity. Methods of preventing or delaying the onset of Alzheimer's disease in a subject are also provided.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . A method of treating or delaying the onset of Alzheimer's disease in a patient having or at risk of developing Alzheimer's disease comprising administering to the subject an effective amount of an anti-angiogenic agent. 
     
     
         2 . A method of maintaining and/or restoring blood-brain barrier (BBB) integrity in a subject having or at risk of developing Alzheimer's disease comprising administering to the subject an effective amount of an anti-angiogenic agent and/or an agent that inhibits abeta amyloidogenesis or promotes removal of abeta peptide from the brain. 
     
     
         3 . A method of promoting vascular reversion in the brain of a subject having or at risk of developing Alzheimer's disease comprising administering to the subject an effective amount of an anti-angiogenic agent and/or an agent that promotes the removal of abeta peptide from the brain. 
     
     
         4 . The method of  claim 1 ,  2  or  3 , wherein the anti-angiogenic agent is bexarotene, bevacizumab (Avastin®), imatinib, sorafenib, sunitinib, leflunomide (SU101), midostaurin (PKC412), vatalinib (PTK787/LK222584), AG013736, AZD2171, CP547,632, CP673,451, RPI.4610, VEGF Trap, ZD6474, YM359445, SU5416, temsirolimus (Toriser), batimastat, marimastat, neovastat, prinomastat, carboxyamidotriazole, TNP-470, CM101, IFN-□, IL-12, platelet factor-4, suramin, SU5416, thrombospondin, angiostatin, endostatin, thalidomide, tetrathiomolybdate, tecogalan, razoxane or reservatrol. 
     
     
         5 . The method of  claim 3 , wherein the agent that promotes the removal of abeta peptide from the brain is abeta peptide, or an antibody that specifically binds abeta peptide. 
     
     
         6 . A method for identifying subjects at risk of developing Alzheimer's disease, or having early stage Alzheimer's disease, comprising detecting neoangiogenesis, TJ disruption and/or blood-brain barrier disruption in the brain of a subject. 
     
     
         7 . A method of identifying potential therapeutic agents for the treatment of Alzheimer's disease comprising testing the ability of a candidate agent to restore tight junctions in cerebral blood vessels or to promote vascular reversion in the brain. 
     
     
         8 . The method according to  claim 7 , comprising the steps of:
 providing a culture of a cell line that forms functional in vitro model of the blood-brain barrier,   contacting the culture with an agent that disrupts tight junctions,   
       contacting the culture with the candidate agent,
 assessing integrity of the tight junctions in the cell culture 
 
       wherein an increase in integrity in the tight junctions compared to a control animal not receiving the candidate agent indicates the agent is a potential therapeutic agent. 
     
     
         9 . The method according to  claim 7 , comprising the steps of:
 administering the candidate agent to an animal model to Alzheimer's disease, and   assessing integrity of the tight junctions in the cerebral blood vessels,   
       wherein an increase in integrity in the tight junctions compared to a control animal not receiving the candidate agent indicates the agent is a potential therapeutic agent.

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