A method of treating a disease or condition associated with elevated human interleukin-6 (IL-6), comprising administering a therapeutically effective amount of an anti-IL-6 antibody or antibody fragment to a subject in need thereof, wherein the antibody or antibody fragment comprises:na variable light chain polypeptide comprising the CDRs of SEQ ID NOs:4, 5 and 6 and possessing at least 90% identity to the variable light chain polypeptide of SEQ ID NO:709, anda variable heavy chain polypeptide comprising the CDRs of SEQ ID NOs:7, 8 or 120, and 9 and possessing at least 90% identity to the variable heavy chain polypeptide of SEQ ID NO:657, and;wherein the antibody or antibody fragment specifically binds to IL-6 and antagonizes one or more activities associated with IL-6 and specifically binds to the same epitope(s) on IL-6 as an anti-IL-6 antibody comprising the variable light chain polypeptide of SEQ ID NO:709 and the variable heavy chain polypeptide of SEQ ID NO:657.
›2.↳ 1The method of claim 1, wherein the variable light chain polypeptide and the variable heavy chain polypeptide each possess at least 95% sequence identi…d2
The method of claim 1, wherein the variable light chain polypeptide and the variable heavy chain polypeptide each possess at least 95% sequence identity to the variable light chain and variable heavy chain polypeptides of SEQ ID NOs: 709 and 657, respectively.
›3.↳ 1The method of claim 1, wherein the variable light chain polypeptide and the variable heavy chain polypeptide each possess at least 97% sequence identi…d2
The method of claim 1, wherein the variable light chain polypeptide and the variable heavy chain polypeptide each possess at least 97% sequence identity to the variable light chain and variable heavy chain polypeptides of SEQ ID NOs: 709 and 657, respectively.
›4.↳ 1The method of claim 1, wherein the antibody or antibody fragment has an in vivo half-life of at least about 22 days in a healthy human subject.d2
The method of claim 1, wherein the antibody or antibody fragment has an in vivo half-life of at least about 22 days in a healthy human subject.
›5.↳ 1The method of claim 1, wherein the antibody or antibody fragment has a binding affinity (Kd) for IL-6 of less than about 50 picomolar, or a rate of di…d2
The method of claim 1, wherein the antibody or antibody fragment has a binding affinity (Kd) for IL-6 of less than about 50 picomolar, or a rate of dissociation (Koff) from IL-6 of less than or equal to 10-4 S-1.
›6.↳ 1The method of claim 1, wherein the antibody or antibody fragment contains an Fc region that has been modified to alter effector function, half-life, p…d2
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.
›7.↳ 1The method of claim 1, wherein the antibody is selected from a humanized, single chain, or chimeric antibody and the antibody fragment is selected fro…d2
The method of claim 1, wherein the antibody is selected from a humanized, single chain, or chimeric antibody and the antibody fragment is selected from a Fab, Fab⬲, F(ab⬲)2, Fv, or scFv.
›8.↳ 1The method of claim 1, wherein the therapeutically effective amount is between about 0.1 and 20 mg/kg of body weight of recipient subject.d2
The method of claim 1, wherein the therapeutically effective amount is between about 0.1 and 20 mg/kg of body weight of recipient subject.
›9.↳ 1The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to gp130.d2
The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to gp130.
›10.↳ 1The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to IL-6R1.d2
The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to IL-6R1.
›11.↳ 1The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to both gp 130 and IL-6R1.d2
The method of claim 1, wherein said anti-IL-6 antibody or fragment inhibits the binding of IL-6 to both gp 130 and IL-6R1.
›12.↳ 1The method of claim 1, wherein said anti-IL-6 antibody or fragment neutralizes IL-6 in vivo.d2
The method of claim 1, wherein said anti-IL-6 antibody or fragment neutralizes IL-6 in vivo.
›13.↳ 1The method of claim 1, wherein the anti-IL-6 antibody or antibody fragment comprises a human constant region.d2+2
The method of claim 1, wherein the anti-IL-6 antibody or antibody fragment comprises a human constant region.
›14.↳ 13The method of claim 13, wherein said human constant region comprises an IgG1, IgG2, IgG3 or IgG4 constant region.d3
The method of claim 13, wherein said human constant region comprises an IgG1, IgG2, IgG3 or IgG4 constant region.
›15.↳ 13The method of claim 13, wherein said human constant region comprises an IgG1 constant region.d3
The method of claim 13, wherein said human constant region comprises an IgG1 constant region.