US2015166660A1PendingUtilityA1

Immunomodulation by anti-cd3 immunotoxins to treat cancers not uniformly bearing surface cd3

Assignee: ANGIMMUNE LLCPriority: Apr 20, 2012Filed: Mar 13, 2013Published: Jun 18, 2015
Est. expiryApr 20, 2032(~5.7 yrs left)· nominal 20-yr term from priority
A61P 35/00C07K 16/30C07K 16/2809A61K 2039/505C07K 2319/00C07K 2317/35C07K 2317/622A61K 39/3955A61K 2039/545A61K 38/164A61K 39/0011A61K 47/6879A61K 47/6829A61K 47/6849C07K 2317/73Y02A50/30
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Claims

Abstract

Methods of modulating the immune systems of patients suffering from cancers that do not hear, or do not uniformly bear, surface CD3 are provided. The methods involve administering an anti-CD3 immunotoxin (e.g. A-dmDT390-bisFv(UCHT1)), to the patient so a to cause the patient's Immune system to recognize and destroy non-CD3 cancer cells.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . A method of providing immunomodulation to a patient suffering from a cancer which does not bear, or does not uniformly bear, surface CD3 epitopes, comprising
 administering to the patient an anti-CD3 specific immunotoxin in an amount sufficient to deplete extant T-cells of said patient; and   allowing repopulation and maturation of new T cells in said patient in the presence of said non-CD3 cancer cell antigens.   
     
     
         2 . The method of  claim 1 , wherein said non-CD3 cancer cell antigens are released into circulation as a result of administering an antigen releasing anti-cancer therapy. 
     
     
         3 . The method of  claim 2 , wherein said antigen releasing anti-cancer therapy is radiation therapy. 
     
     
         4 . The method of  claim 1 , wherein said step of administering does not break immune tolerance to self antigens in said patient. 
     
     
         5 . The method of  claim 1  further comprising a step of providing said non-CD3 cancer cell antigens to said patient to boost an immune response of said patient to said non-CD3 cancer cell antigens, at a period of time after said step of allowing. 
     
     
         6 . The method of  claim 5 , wherein said step of providing is performed after a recurrence of said cancer. 
     
     
         7 . The method of  claim 1 , wherein said anti-CD3 specific immunotoxin is A-dmDT390-bisFv (UCHT1). 
     
     
         8 . A method of lengthening survival time of a patient suffering from a cancer which does not bear, or does not uniformly bear, surface CD3 epitopes, comprising
 administering to the patient an anti-CD3 specific immunotoxin in an amount sufficient to deplete extant T-cells of said patient; and   allowing repopulation and maturation of new T cells in said patient in the presence of said non-CD3 cancer cell antigens.   
     
     
         9 . A method of preparing the immune system of a patient to recognize and kill metastatic and/or recurrent cancer, wherein said patient is suffering from a cancer which does not bear, or does not uniformly bear, surface CD3 epitopes, comprising
 administering to the patient an anti-CD3 specific immunotoxin in an amount sufficient to deplete extant T-cells of said patient; and   allowing repopulation and maturation of new T cells in said patient in the presence of said non-CD3 cancer cell antigens.

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