| CPC C07K 16/244 (2013.01) [C07K 16/00 (2013.01); C12N 5/0037 (2013.01); C12P 21/005 (2013.01); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/41 (2013.01); C07K 2317/56 (2013.01); C07K 2317/565 (2013.01); C07K 2317/76 (2013.01); C12N 2500/02 (2013.01); C12N 2500/12 (2013.01); C12N 2500/32 (2013.01); C12N 2500/34 (2013.01); C12N 2500/38 (2013.01); C12N 2500/60 (2013.01); C12N 2500/74 (2013.01); C12N 2500/76 (2013.01)] | 6 Claims |
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1. A method of treating celiac disease, comprising administering to a subject a composition comprising an antibody or an antigen-binding fragment thereof,
wherein fewer than about 10% of the antibody or antigen-binding fragment molecules in the composition have more than 4 mannose residues per N-linked oligosaccharide, and
wherein the antibody or antigen-binding fragment thereof comprises:
a light chain variable region comprising the CDRs of the light chain variable region sequence set forth in SEQ ID NO:4, and
a heavy chain variable region comprising the CDRs of the heavy chain variable region sequence set forth in SEQ ID NO:2.
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