Methods of aiding in the diagnosis of diseases using anti-IL-6 antibodies
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 aiding in the diagnosis of a disease or condition associated with elevated interleukin 6 (“IL-6”), comprising detecting for the presence of elevated amounts of IL-6 in a biological sample of a subject, and if said biological sample is determined to comprise elevated IL-6 levels identifying said subject as one having or suspected of having a disease associated with elevated IL-6, wherein said detection is effected by:
(i) contacting a biological sample of the patient putatively having a condition associated with elevated IL-6 with an amount of an anti-IL-6 antibody or antibody fragment, whereby said amount of antibody or antibody fragment binds to any IL-6 in the biological sample, wherein the antibody or antibody fragment comprises: a variable light chain polypeptide comprising: a polypeptide having at least 90% identity to SEQ ID NO: 709, and a variable heavy chain polypeptide comprising: a polypeptide having at least 90% identity to SEQ ID NO: 657, further wherein said anti-IL-6 antibody or antibody fragment comprises the variable light chain complementarity determining region (CDR) polypeptides of SEQ ID NO:4, 5 and 6 and comprises the variable heavy chain complementarity determining region (CDR) polypeptides of SEQ ID NO:7, 8 or 120, and 9 and
(ii) detecting the binding of any IL-6 present in the sample to said anti-IL-6 antibody or antibody fragment in order to determine whether the subject putatively has a condition associated with elevated IL-6.
2. The method of claim 1 , wherein the light chain possesses at least 95% sequence identity to the light chain polypeptide comprised in SEQ ID NO: 709.
3. The method of claim 1 , wherein the heavy chain possesses at least 95% sequence identity to the heavy chain polypeptide comprised in SEQ ID NO: 657.
4. The method of claim 1 , wherein the light chain possesses at least 97% sequence identity to the light chain polypeptide comprised in SEQ ID NO: 709.
5. The method of claim 1 , wherein the heavy chain possesses at least 97% sequence identity to the heavy chain polypeptide comprised in SEQ ID NO: 657.
6. The method of claim 1 , wherein the light chain possesses at least 99% sequence identity to the light chain polypeptide comprised in SEQ ID NO: 709.
7. The method of claim 1 , wherein the heavy chain possesses at least 99% sequence identity to the heavy chain polypeptide comprised in SEQ ID NO: 657.
8. The method of claim 1 , wherein the light chain possesses 100% sequence identity to the light chain polypeptide comprised in SEQ ID NO: 709.
9. The method of claim 1 , wherein the heavy chain possesses 100% sequence identity to the heavy chain polypeptide comprised in SEQ ID NO: 657.
10. The method of claim 1 wherein said antibody comprises light chain CDR1, CDR2 and CDR3 polypeptides and heavy chain CDR1, CDR2 and CDR3 identical to those on SEQ ID NO:4, 5 and 6 and SEQ ID NO:7, 120 and 9 respectively.
11. The method of claim 1 wherein said antibody comprises light chain CDR1, CDR2 and CDR3 polypeptides and heavy chain CDR1, CDR2 and CDR3 polypeptides identical to those on SEQ ID NO:4, 5 and 6 and SEQ ID NO:7, 8 and 9 respectively.
12. The method of claim 1 wherein said biological sample is selected from sera, plasma, urine, saliva, mucous, pleural fluid, synovial fluid and spinal fluid.
13. The method of claim 1 wherein said biological sample is sera or plasma.
14. The method of claim 1 wherein said detection is effected in vitro.
15. The method of claim 1 wherein said detection is effected in vivo.
16. The method of claim 1 wherein said method further includes the detection of a clinical marker other than IL-6.
17. The method of claim 16 , wherein the other clinical marker is a compound correlated to inflammation.
18. The method of claim 1 wherein the antibody is selected from a human, humanized, single chain, or chimeric antibody and the antibody fragment is selected from a Fab, Fab′, F(ab′) 2 , Fv, or scFv.
19. The method claim 1 wherein the disease or condition associated with elevated IL-6 is selected from cancer, a disease or condition associated with hypercoagulation, a disease or condition associated with elevated serum CRP, a disease or condition associated with hypoalbuminemia, an inflammatory disorder, a viral disorder, a wasting syndrome, an autoimmune disorder or any combination thereof.