Antagonists of IL-6 to prevent or treat cachexia, weakness, fatigue, and/or fever
View Patent ↗The present invention is directed to therapeutic methods using antibodies and fragments thereof having binding specificity for IL-6 to prevent or treat cachexia, fever, weakness and/or fatigue in 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. In another preferred embodiment, the patient's survivability or quality of life will preferably be improved.
1. A method of inhibiting interleukin 6 (IL-6)-associated cachexia, weakness, fever or fatigue in a patient in need thereof by administering an anti-human IL-6 antibody or anti-human IL-6 antibody fragment which comprises the variable light chain (V L ) complementarity determining regions (CDRs) of SEQ ID NO:4, 5 and 6 and the variable heavy chain (V H ) complementarity determining regions (CDRs) of SEQ ID NO:7, 8 or 120, and 9.
2. The method of claim 1 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises the variable light chain (V L ) complementarity determining regions (CDRs) of SEQ ID NO:4, 5 and 6 and the variable heavy chain (V H ) complementarity determining regions (CDRs) of SEQ ID NO:7, 120, and 9.
3. The method of claim 2 wherein the patient has a chronic inflammatory condition.
4. The method of claim 1 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises the variable light chain (V L ) polypeptide SEQ ID NO:20 and the variable heavy chain (V H ) polypeptide of SEQ ID NO:19 or 18.
5. The method of claim 4 wherein the patient has a chronic inflammatory condition.
6. The method of claim 1 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises the variable light chain (V L ) polypeptide SEQ ID NO:20 and the variable heavy chain (V H ) polypeptide of SEQ ID NO:19.
7. The method of claim 6 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises a human IgG1 constant region polypeptide.
8. The method of claim 7 wherein the human IgG1 constant region polypeptide is mutated to reduce or eliminate FcR binding or glycosylation.
9. The method of claim 6 wherein the patient has a chronic inflammatory condition.
10. The method of claim 1 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises a human IgG1, IgG2, IgG3 or IgG4 constant region polypeptide.
11. The method of claim 10 wherein the human IgG1, IgG2, IgG3 or IgG4 constant region polypeptide is mutated to reduce or eliminate FcR binding or glycosylation.
12. The method of claim 1 wherein the patient's cachexia is stabilized or improved after anti-IL-6 antibody administration.
13. The method of claim 1 wherein the anti-human IL-6 antibody or anti-human IL-6 antibody fragment comprises a human IgG1 constant region polypeptide.
14. The method of claim 13 wherein the human IgG1 constant region polypeptide is mutated to reduce or eliminate FcR binding or glycosylation.
15. The method of claim 1 wherein the patient has a chronic inflammatory condition.