US2015132326A1PendingUtilityA1

Immunosuppressive blood cells and methods of producing the same

Assignee: UNIVERSITATSKLINIKUM HEIDELBERGPriority: Jun 30, 2008Filed: Nov 7, 2014Published: May 14, 2015
Est. expiryJun 30, 2028(~1.9 yrs left)· nominal 20-yr term from priority
A61P 37/06A61P 29/00C12N 2501/06A61K 39/0008A61K 31/5377A61K 38/1709A61K 35/14A61K 31/164A61K 31/7072A61K 2035/122A61K 31/407A61K 38/16A61K 40/416A61K 40/24A61K 40/22A61K 40/19A61K 40/10A61K 39/00C12N 5/0634
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Claims

Abstract

The present invention refers to a method of producing immunosuppressive blood cells that can be used for the treatment of autoimmune diseases, in particular multiple sclerosis, organ graft rejection and graft-versus-host disease.

Claims

exact text as granted — not AI-modified
1 - 15 . (canceled) 
     
     
         16 . A method of producing immunosuppressive blood cells comprising:
 (a) exposing an isolated blood cell sample to a chemotherapeutic agent; and   (b) optionally exposing the isolated blood cell sample to an autoantigen or a derivative thereof.   
     
     
         17 . The method according to  claim 16 , wherein the exposure takes place in vitro. 
     
     
         18 . The method according to  claim 17 , wherein the blood cell sample is first treated with the autoantigen and subsequently with the chemotherapeutic agent. 
     
     
         19 . A method for treating a patient suffering from an autoimmune disease, the method comprising:
 (a) obtaining a blood cell sample;   (b) treating the blood cell sample with a chemotherapeutic agent and an autoantigen; and   (c) administering such treated blood cells to the patient;   wherein the treated blood cells ameliorate the autoimmune disease in the patient.   
     
     
         20 . A method for treating an inflammatory disease, organ graft rejection or graft-versus-host disease in a patient comprising administering to the patient a composition comprising
 (a) isolated blood cells treated with a therapeutically effective amount of a chemotherapeutic agent and optionally an autoantigen or a derivative thereof, and   (b) optionally a pharmaceutically acceptable carrier.   
     
     
         21 . The method of  claim 20 , wherein the chemotherapeutic agent is selected from the group consisting of mitomycin C, C2 ceramide, tunicamycin, mycophenolate-mofetil, tryptophan metabolites, semisynthetic derivates thereof, proteasome inhibitors, and a combination of two or more agents. 
     
     
         22 . The method of  claim 21 , wherein the chemotherapeutic agent is mitomycin C. 
     
     
         23 . The method of  claim 20 , wherein the autoantigen is selected from the group consisting of natural antigens, synthetic peptides and natural peptides. 
     
     
         24 . The method of  claim 23 , wherein the autoantigen is a synthetic peptide of the myelin basic protein. 
     
     
         25 . The method of  claim 24 , wherein the synthetic peptide of the myelin basic protein is copaxone. 
     
     
         26 . The method of  claim 20 , wherein the disease is organ graft rejection or graft-versus-host disease and the blood cells are only treated with a chemotherapeutic agent. 
     
     
         27 . The method of  claim 26 , wherein the chemotherapeutic agent is mitomycin C. 
     
     
         28 . The method of  claim 20 , wherein the isolated blood cells are whole blood or peripheral blood mononuclear cells.

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