N-glycosylation heterogeneity and the influence on structure, function and pharmacokinetics of monoclonal antibodies and Fc fusion proteins

被引:249
作者
Higel, Fabian [1 ]
Seidl, Andreas [1 ]
Soergel, Fritz [2 ,3 ]
Friess, Wolfgang [4 ]
机构
[1] HEXAL AG, Sandoz Biopharmaceut, Oberhaching, Germany
[2] IBMP Inst Biomed & Pharmaceut Res, Nuernberg Heroldsberg, Germany
[3] Univ Duisburg Essen, Fac Med, Inst Pharmacol, Essen, Germany
[4] Univ Munich, Dept Pharm Pharmaceut Technol & Biopharmaceut, Munich, Germany
关键词
Monoclonal antibody; Fusion protein; N-glycosylation; Pharmacokinetics; Glyco-engineering; CHROMATOGRAPHY-MASS SPECTROMETRY; VARIABLE DOMAIN GLYCOSYLATION; HOST-CELL LINE; LIQUID-CHROMATOGRAPHY; THERAPEUTIC ANTIBODIES; EFFECTOR FUNCTIONS; IMMUNOGLOBULIN-G; GLYCAN ANALYSIS; COMPLEX GLYCOPROTEIN; MANNOSE RECEPTOR;
D O I
10.1016/j.ejpb.2016.01.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Monoclonal antibody and Fc fusion protein drugs are complex heterogeneous mixtures of numerous different protein variants and modifications. N-glycosylation as one of the most complex post translational modification influences the structural characteristics of the antibodies Fc part thereby potentially modulating effector function and pharmacokinetics. Several investigations on the relationship between N-glycosylation and pharmacokinetics have been published. However, this structure-function relationship is not fully understood. In this review potential alterations with focus on N-glycosylation of mAbs and Fc fusion proteins and the possible effects on the pharmacokinetics are reviewed and the current understandings of the underlying mechanisms are described. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:94 / 100
页数:7
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