Antibodies to IL-6 and use thereof
View Patent ↗The present invention is directed to therapeutic methods using IL-6 antagonists such as an Ab1 antibody or antibody fragment having binding specificity for IL-6 to prevent or treat disease or to improve survivability or quality of life of a patient in need thereof. In preferred embodiments these patients will comprise those exhibiting (or at risk of developing) an elevated serum C-reactive protein level, reduced serum albumin level, elevated D-dimer or other coagulation cascade related protein(s), cachexia, fever, weakness and/or fatigue prior to treatment. The subject therapies also may include the administration of other actives such as chemotherapeutics, anti-coagulants, statins, and others.
1. A method of treating a chronic disease associated with reduced hemoglobulin comprising administration of an anti-interleukin-6 (“IL-6”) antibody or antibody fragment to a subject in need thereof, wherein the antibody or antibody fragment comprises a variable light (V L ) chain having the complementarity determining regions (CDRs) of SEQ ID NO:4, 5 and 6, and a variable heavy (V H ) chain having the CDRs of SEQ ID NO:7, 8 or 120, and 9, respectively, and wherein the administration of said antibody increases or maintains the hemoglobin levels in said patient.
2. The method of claim 1 , which comprises detecting hemoglobin levels before treatment.
3. The method of claim 1 , which comprises detecting hemoglobin levels after treatment.
4. The method of claim 1 , which comprises detecting hemoglobin levels before and after treatment.
5. The method of claim 1 , wherein the antibody or antibody fragment comprises (a) a V L chain polypeptide sequence which is at least 90% identical to the polypeptide sequences of SEQ ID NO:699, SEQ ID NO:20 or SEQ ID NO:2, and (b) a V H chain polypeptide sequence which is at least 90% identical to the polypeptide sequences of SEQ ID NO:657, SEQ ID NO:19, or SEQ ID NO:3.
6. The method of claim 1 , wherein said antibody or antibody fragment is selected from the group consisting of Fab, Fab′, F(ab′)2, Fv, IgNAR, SMIP, camelbodies, nanobodies and scFvs.
7. The method of claim 1 , wherein said antibody or antibody fragment is selected from the group consisting of human, chimeric and humanized antibodies and fragments thereof.
8. The method of claim 1 , wherein the antibody or antibody fragment comprises (a) a VL chain polypeptide sequence which is at least 95% identical to the polypeptide sequences of SEQ ID NO:699, SEQ ID NO:20 or SEQ ID NO:2, and (b) a VH chain polypeptide sequence which is at least 95% identical to the polypeptide sequences of SEQ ID NO:657, SEQ ID NO:19, or SEQ ID NO:3.
9. The method of claim 1 , wherein the antibody or antibody fragment comprises (a) a VL chain polypeptide sequence which is at least 98% identical to the polypeptide sequences of SEQ ID NO:699, SEQ ID NO:20 or SEQ ID NO:2, and (b) a VH chain polypeptide sequence which is at least 98% identical to the polypeptide sequences of SEQ ID NO:657, SEQ ID NO:19, or SEQ ID NO:3.
10. The method of claim 1 , wherein the antibody or antibody fragment comprises (a) a VL chain polypeptide sequence which is identical to the polypeptide sequences of SEQ ID NO:699, SEQ ID NO:20 and or SEQ ID NO:2, and (b) a VH chain polypeptide sequence which is identical to the polypeptide sequences of SEQ ID NO:657, SEQ ID NO:19, or SEQ ID NO:3.
11. The method of claim 10 , wherein said antibody or antibody fragment is selected from the group consisting of Fab, Fab′, F(ab′) 2 , Fv, IgNAR, SMIP, camelbodies, nanobodies and scFvs.
12. The method of claim 10 , wherein said antibody or antibody fragment is selected from the group consisting of human, chimeric and humanized antibodies and fragments thereof.
13. The method of claim 1 , wherein the antibody or antibody fragment is non-glycosylated.
14. The method of claim 1 , wherein the antibody or antibody fragment contains an Fc region that has been modified to alter effector function, half-life, proteolysis, and/or glycosylation.
15. The method of claim 1 , wherein said antibody is an IgG1.
16. The method of claim 1 , wherein the antibody or antibody fragment comprises (a) a light chain polypeptide sequence which is identical to the polypeptide sequences of SEQ ID NO:702 or SEQ ID NO:706, and (b) a heavy chain polypeptide sequence which is identical to the polypeptide sequences of SEQ ID NO:704 or SEQ ID NO:708.
17. The method of claim 1 , wherein said antibody is administered intravenously or subcutaneously.
18. The method of claim 1 , wherein the antibody is administered at a frequency of at most once per period of approximately four weeks, approximately eight weeks, approximately twelve weeks, approximately sixteen weeks, approximately twenty weeks, or approximately twenty-four weeks.