Antagonists of IL-6 to prevent or treat cachexia, weakness, fatigue, and /or fever
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, the anti-IL-6 antibodies will be humanized and/or will be aglycosylated. Also, 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 treating cardiac-related cachexia, respiratory-related cachexia, renal-related cachexia or age-related cachexia comprising administering to the patient an effective amount of an anti-IL-6 antibody or antibody fragment comprising variable heavy and variable light chain sequences respectively contained in SEQ ID NO:657 and SEQ ID NO:709.
2. The method of claim 1 , which further comprises detecting cardiac-related cachexia, respiratory-related cachexia, renal-related cachexia or age-related cachexia in the patient before, during or after antibody administration.
3. The method of claim 1 , wherein the cachexia comprises respiratory-related cachexia.
4. The method of claim 1 , wherein the cachexia comprises renal-related cachexia.
5. The method of claim 1 , wherein the cachexia comprises cardiac-related cachexia.
6. The method of claim 1 , wherein the cachexia comprises age-related cachexia.
7. The method of claim 1 , wherein the anti-IL-6 antibody or antibody fragment comprises human IgG1 constant regions.
8. The method of claim 7 , wherein the human IgG1 constant region comprises the light constant chain polypeptide of SEQ ID NO: 586 and heavy constant chain polypeptide of SEQ ID NO:588.
9. The method of claim 1 , wherein the anti-IL-6 antibody or antibody fragment is administered to the patient with a frequency of at most once per period of approximately four weeks.
10. The method of claim 1 , wherein the anti-IL-6 antibody or antibody fragment is administered to the patient with a frequency of at most once per period of approximately eight weeks.
11. The method of claim 1 , wherein the anti-IL-6 antibody or antibody fragment is administered to the patient with a frequency of at most once per period of approximately twelve weeks.
12. The method of claim 1 , wherein the anti-IL-6 antibody or antibody fragment is administered to the patient with a frequency of at most once per period of approximately sixteen weeks.