Safety and Efficacy with a CHO Cell Glycosylated Chimeric Antibody to TNF
20170247443 · 2017-08-31
Assignee
Inventors
Cpc classification
C07K2317/41
CHEMISTRY; METALLURGY
A61P29/00
HUMAN NECESSITIES
C07K2317/51
CHEMISTRY; METALLURGY
A61P35/00
HUMAN NECESSITIES
International classification
Abstract
There is disclosed a chimeric infliximab-like monoclonal antibody having at least 80% NANA glycosylation terminal sialic acid and a glycosylation pattern of Gal-α(2,3/6)-Gal that binds to tumor necrosis factor alpha (TNF). The disclosed infliximab-like monoclonal antibody is a chimeric antibody having the same amino acid sequence (light chain/heavy chain of SEQ ID NO. 1/SEQ ID NO. 2) as infliximab (Remicade®) which has at least 80% NGNA terminal sialic acid and a glycosylation pattern of Gal-α(1,3)-Gal.
Claims
1. A pharmaceutical composition comprising an anti-TNF antibody, wherein the anti-TNF antibody comprises a light chain comprising the amino acid sequence set forth in SEQ ID NO: 1 and a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 2, and wherein the anti-TNF antibody comprises a glycosylation pattern having at least 80% NGNA terminal sialic acid and a glycosylation pattern of Gal-α(1,3)-Gal n.
2. The pharmaceutical composition of claim 1, wherein the z-avg of the antibody is 15-20 nm.
3. The pharmaceutical composition of claim 1, wherein the sialic acid glycosylation is at least 80% NANA glycosylation terminal sialic acid at an N-glycosylation site.
Description
DESCRIPTION OF THE DRAWINGS
[0009]
[0010]
[0011]
[0012]
DETAILED DESCRIPTION
[0013] The invention is based, at least in part, on the therapeutic advantages of producing an anti-TNF antibody in Chinese Hamster Ovary (CHO) cells. STI002 is an anti-TNF antibody that is produced in CHO cells and has the amino acid sequence of infliximab. Structurally, infliximab has a light chain comprising the amino acid sequence set forth in SEQ ID NO: 1, and a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 2. The amino acid sequences of the infliximab light and heavy chains are described below:
TABLE-US-00001 (SEQ ID NO: 1) Asp Ile Leu Leu Thr Gln Ser Pro Ala Ile Leu Ser Val Ser Pro Gly Glu Arg Val Ser Phe Ser Cys Arg Ala Ser Gln Phe Val Gly Ser Ser Ile His Trp Tyr Gln Gln Arg Thr Asn Gly Ser Pro Arg Leu Leu Ile Lys Tyr Ala Ser Glu Ser Met Ser Gly Ile Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Ser Ile Asn Thr Val Glu Ser Glu Asp Ile Ala Asp Tyr Tyr Cys Gln Gln Ser His Ser Trp Pro Phe Thr Phe Gly Ser Gly Thr Asn Leu Glu Val Lys SEQ ID NO: 2) Glu Val Lys Leu Glu Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly Ser Met Lys Leu Ser Cys Val Ala Ser Gly Phe Ile Phe Ser Asn His Trp Met Asn Trp Val Arg Gln Ser Pro Glu Lys Gly Leu Glu Trp Val Ala Glu Ile Arg Ser Lys Ser Ile Asn Ser Ala Thr His Tyr Ala Glu Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Ser Ala Val Tyr Leu Gln Met Thr Asp Leu Arg Thr Glu Asp Thr Gly Val Tyr Tyr Cys Ser Arg Asn Tyr Tyr Gly Ser Thr Tyr Asp Tyr Trp Gly Gln Gly Thr Thr Leu Thr Val Ser
[0014] Thus, the infliximab-like antibody comprises a light chain comprising the amino acid sequence set forth in SEQ ID NO: 1 and a heavy chain comprising the amino acid sequence set forth in SEQ ID NO: 2. Further, the infliximab-like antibody does not contain either an N-glycolylneuraminic acid (NGNA) glycan or a Gal-α(1,3)-Gal glycan. The infliximab-like antibody does contain glycans associated with CHO cell expression, including, for example, a Gal-α(2, 3/6)-Gal glycan.
[0015] The glycosylation mechanism in CHO cells is similar to an IgG glycosylation mechanism in human The present disclosure provides a genetically engineered anti-TNF antibody with different glycan structures than infliximab. By structure analysis, it was determined the infliximab glycan contains primarily α-Gal, and mostly NGNA as the terminal sialic acid. NGNA has very high immunogenicity. At the same time of greatly reduced immunogenicity, the characteristics of the disclosed infliximab-like monoclonal antibody in vivo clearance is in line with the in vivo metabolic of chimeric antibodies, and the pharmacokinetic parameters are consistent with those of infliximab.
[0016] Compared with infliximab monoclonal antibody, the disclosed monoclonal antibody has the same amino acid primary structure but does not contain α-Gal. Moreover, the terminal sialic acid is mainly N-acetylneuraminic acid (NANA). These glycosylation changes provide an improvement manifest with better patient tolerance. A clinical study of the disclosed antibody showed better patient tolerance and reduced immunogenicity when compared with published historical data with commercial infliximab. The disclosed monoclonal antibody also showed similar pharmacokinetic in vivo clearance and in vivo metabolism as infliximab according to its commercial product disclosed data.
[0017] The present disclosure provides a chimeric monoclonal antibody having at least 80% NANA glycosylation terminal sialic acid at an N-glycosylation site and a glycosylation pattern of Gal-α(2,3/6)-Gal.
[0018] Efficacy was also measured and compared in vitro.