US2019112384A1PendingUtilityA1

Compositions and methods for the detection diagnosis and therapy of hematological malignancies

72
Assignee: CORIXA CORPPriority: Jan 22, 2002Filed: Dec 17, 2018Published: Apr 18, 2019
Est. expiryJan 22, 2022(expired)· nominal 20-yr term from priority
A61K 47/6851C07K 14/47C12Q 2600/158C12Q 2600/112A61K 2039/505C12Q 2600/106C07K 2317/55C07K 2317/92C12N 15/11C12Q 1/6886A61K 38/00C07K 14/70535C12N 5/06C12Q 2600/118C07K 2317/24C07K 2317/56C07K 2317/569C07K 16/3061C07K 16/28C12N 15/63A61P 35/00A61K 51/1018C07K 16/18G01N 33/57505G01N 33/57426A61K 39/0011A61K 39/00A61K 40/416A61K 40/42A61K 40/22A61K 40/11A61K 2239/48
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Claims

Abstract

Disclosed are methods and compositions for the detection, diagnosis, prognosis, and therapy of hematological malignancies, and in particular, B cell leukemias, lymphomas and multiple myelomas. Disclosed are compositions, methods and kits for eliciting immune and T cell responses to specific malignancy-related antigenic polypeptides and antigenic polypeptide fragments thereof in an animal. Also disclosed are compositions and methods for use in the identification of cells and biological samples containing one or more hematological malignancy-related compositions, and methods for the detection and diagnosis of such diseases and affected cell types. Also disclosed are diagnostic and therapeutic kits, as well as methods for the diagnosis, therapy and/or prevention of a variety of leukemias and lymphomas.

Claims

exact text as granted — not AI-modified
1 - 16 . (canceled) 
     
     
         17 . A method for treating cancer in a mammalian subject wherein a B-cell from the subject overexpresses SEQ ID NO:4 comprising, administering to the subject an effective amount of an antibody that specifically binds to a polypeptide comprising the sequence set forth in SEQ ID NO: 4, wherein the cancer is multiple myeloma. 
     
     
         18 . The method of  claim 17 , wherein the antibody is a humanized antibody. 
     
     
         19 . The method of  claim 17 , wherein the antibody is a monoclonal antibody. 
     
     
         20 . The method of  claim 17 , wherein the mammalian subject is a human. 
     
     
         21 . The method of  claim 17 , wherein administration is intravenous. 
     
     
         22 . The method of  claim 17 , wherein the antibody is coupled to a therapeutic agent. 
     
     
         23 . The method of  claim 22 , wherein the therapeutic agent is a cytotoxic agent. 
     
     
         24 . The method of  claim 22 , wherein the therapeutic agent is a chemotherapeutic agent. 
     
     
         25 . The method of  claim 22 , wherein the therapeutic agent is coupled to the antibody via a linker. 
     
     
         26 . The method of  claim 17 , wherein the antibody is an immunotherapeutic antibody. 
     
     
         27 . The method of  claim 26 , wherein the antibody is a passive immunotherapeutic antibody. 
     
     
         28 . The method of  claim 27 , wherein the passive immunotherapeutic antibody directly or indirectly mediates antitumor effect and does not necessarily depend on an intact host immune system. 
     
     
         29 . The method of  claim 26 , wherein the antibody is an active immunotherapeutic antibody. 
     
     
         30 . The method of  claim 29 , wherein the active immunotherapeutic antibody relies on in vivo stimulation of the endogenous host immune system against the cancer cells.

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