US2012244167A1PendingUtilityA1

Antibodies to m-csf

60
Assignee: BEDIAN VAHEPriority: Sep 10, 2003Filed: Apr 27, 2012Published: Sep 27, 2012
Est. expirySep 10, 2023(expired)· nominal 20-yr term from priority
A61P 9/10A61P 7/02A61P 39/02A61P 37/08A61P 9/00A61P 37/06A61P 37/00A61P 3/10A61P 43/00A61P 33/06A61P 25/00A61P 35/02A61P 31/04A61P 3/00A61P 29/00A61P 25/28A61P 35/00A61P 27/02A61P 11/06A61P 17/02A61P 17/06A61P 19/08A61P 17/04A61P 11/00A61P 19/10A61P 17/00A61P 1/00A61P 21/00A61P 19/06A61P 19/00A61P 13/12A61P 1/04A61P 19/02A61P 17/16G06Q 30/02C07K 16/243C07K 2317/92G06Q 30/0601C07K 2317/56G06Q 40/04A61K 2039/505C07K 2317/14C07K 2317/73C07K 16/24C07K 2317/565C07K 2317/76A61K 38/193A61K 39/395G06Q 50/12C07K 2317/21C07K 16/18Y02A50/30
60
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Claims

Abstract

The present invention relates to antibodies and antigen-binding portions thereof that specifically bind to a M-CSF, preferably human M-CSF, and that function to inhibit a M-CSF. The invention also relates to human anti-M-CSF antibodies and antigen-binding portions thereof. The invention also relates to antibodies that are chimeric, bispecific, derivatized, single chain antibodies or portions of fusion proteins. The invention also relates to isolated heavy and light chain immunoglobulins derived from human anti-M-CSF antibodies and nucleic acid molecules encoding such immunoglobulins. The present invention also relates to methods of making human anti-M-CSF antibodies, compositions comprising these antibodies and methods of using the antibodies and compositions for diagnosis and treatment. The invention also provides gene therapy methods using nucleic acid molecules encoding the heavy and/or light immunoglobulin molecules that comprise the human anti-M-CSF antibodies. The invention also relates to transgenic animals and transgenic plants comprising nucleic acid molecules of the present invention.

Claims

exact text as granted — not AI-modified
1 - 34 . (canceled) 
     
     
         35 . A monoclonal antibody or an antigen-binding portion thereof that specifically binds to M-CSF, wherein the antibody comprises a heavy chain amino acid sequence that is at least 90% identical to the heavy chain amino acid sequence of SEQ ID NO: 30 without the signal sequence. 
     
     
         36 . The monoclonal antibody or antigen-binding portion according to  claim 35 , wherein the antibody further comprises a light chain amino acid sequence of SEQ ID NO: 32 without the signal sequence. 
     
     
         37 . The monoclonal antibody or antigen-binding portion according to  claim 35 , wherein the heavy chain comprises an amino acid sequence that is at least 95% identical to the heavy chain amino acid sequence of SEQ ID NO: 30 without the signal sequence. 
     
     
         38 . A pharmaceutical composition, comprising the antibody or antigen-binding portion according to  claim 35  and a pharmaceutically acceptable carrier. 
     
     
         39 . The monoclonal antibody or antigen-binding portion according to  claim 37 , wherein the heavy chain comprises an amino acid sequence that is at least 99% identical to the heavy chain amino acid sequence of SEQ ID NO: 30 without the signal sequence. 
     
     
         40 . An isolated cell line that produces the antibody or antigen-binding portion according to  claim 36 , or the heavy chain or light chain of said antibody. 
     
     
         41 . The antigen-binding portion according to  claim 35 , wherein the portion is selected from the group consisting of: an Fab fragment, an F(ab′) 2  fragment, and an Fv fragment. 
     
     
         42 . A monoclonal antibody or an antigen-binding portion thereof that specifically binds to M-CSF, wherein the antibody comprises a light chain amino acid sequence that is at least 90% identical to the light chain amino acid sequence of SEQ ID NO: 32 without the signal sequence. 
     
     
         43 . The monoclonal antibody or antigen-binding portion according to  claim 42 , wherein the antibody further comprises a heavy chain amino acid sequence of SEQ ID NO: 30 without the signal sequence. 
     
     
         44 . The monoclonal antibody or antigen-binding portion according to  claim 42 , wherein the light chain comprises an amino acid sequence that is at least 95% identical to the light chain amino acid sequence of SEQ ID NO: 32 without the signal sequence. 
     
     
         45 . A pharmaceutical composition, comprising the antibody or antigen-binding portion according to  claim 42  and a pharmaceutically acceptable carrier. 
     
     
         46 . The monoclonal antibody or antigen-binding portion according to  claim 44 , wherein the light chain comprises an amino acid sequence that is at least 99% identical to the light chain amino acid sequence of SEQ ID NO: 32 without the signal sequence. 
     
     
         47 . An isolated cell line that produces the antibody or antigen-binding portion according to  claim 43 , or the heavy chain or light chain of said antibody. 
     
     
         48 . The antigen-binding portion according to  claim 42 , wherein the portion is selected from the group consisting of: an Fab fragment, an F(ab′) 2  fragment, and an Fv fragment. 
     
     
         49 . A monoclonal antibody or an antigen-binding portion thereof that specifically binds to M-CSF, wherein the antibody comprises a heavy chain amino acid sequence that is at least 90% identical to the heavy chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         50 . The monoclonal antibody or antigen-binding portion according to  claim 49 , wherein the antibody further comprises a light chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         51 . The monoclonal antibody or antigen-binding portion according to  claim 49 , wherein the heavy chain comprises an amino acid sequence that is at least 95% identical to the heavy chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         52 . A pharmaceutical composition, comprising the antibody or antigen-binding portion according to  claim 49  and a pharmaceutically acceptable carrier. 
     
     
         53 . The monoclonal antibody or antigen-binding portion according to  claim 51 , wherein the heavy chain comprises an amino acid sequence that is at least 99% identical to the heavy chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         54 . An isolated cell line that produces the antibody or antigen-binding portion according to  claim 50 , or the heavy chain or light chain of said antibody. 
     
     
         55 . The antigen-binding portion according to  claim 49 , wherein the portion is selected from the group consisting of: an Fab fragment, an F(ab′) 2  fragment, and an Fv fragment. 
     
     
         56 . A monoclonal antibody or an antigen-binding portion thereof that specifically binds to M-CSF, wherein the antibody comprises a light chain amino acid sequence that is at least 90% identical to the light chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         57 . The monoclonal antibody or antigen-binding portion according to  claim 56 , wherein the antibody further comprises a heavy chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         58 . The monoclonal antibody or antigen-binding portion according to  claim 56 , wherein the light chain comprises an amino acid sequence that is at least 95% identical to the light chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         59 . A pharmaceutical composition, comprising the antibody or antigen-binding portion according to  claim 56  and a pharmaceutically acceptable carrier. 
     
     
         60 . The monoclonal antibody or antigen-binding portion according to  claim 58 , wherein the light chain comprises an amino acid sequence that is at least 99% identical to the light chain amino acid sequence of monoclonal antibody 8.10.3F. 
     
     
         61 . An isolated cell line that produces the antibody or antigen-binding portion according to  claim 57 , or the heavy chain or light chain of said antibody. 
     
     
         62 . The antigen-binding portion according to  claim 56 , wherein the portion is selected from the group consisting of: an Fab fragment, an F(ab′) 2  fragment, and an Fv fragment.

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