• Biochim. Biophys. Acta · Aug 2016

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    Immune recruitment or suppression by glycan engineering of endogenous and therapeutic antibodies.

    • Ngoc Phuong Lan Le, Thomas A Bowden, Weston B Struwe, and Max Crispin.
    • Oxford Glycobiology Institute, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, United Kingdom.
    • Biochim. Biophys. Acta. 2016 Aug 1; 1860 (8): 1655-68.

    AbstractHuman serum IgG contains multiple glycoforms which exhibit a range of binding properties to effector molecules such as cellular Fc receptors. Emerging knowledge of how the Fc glycans contribute to the antibody structure and effector functions has opened new avenues for the exploitation of defined antibody glycoforms in the treatment of diseases. Here, we review the structure and activity of antibody glycoforms and highlight developments in antibody glycoengineering by both the manipulation of the cellular glycosylation machinery and by chemoenzymatic synthesis. We discuss wide ranging applications of antibody glycoengineering in the treatment of cancer, autoimmunity and inflammation. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

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