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Improving Immunotherapy Through Glycodesign

delete2018-11-02
delete51
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OA
AI
M
Matthew J. Buettner
S
Sagar Shah
C
Christopher T. Saeui
R
Ryan Ariss
K
Kevin J. Yarema *
DOI:10.3389/fimmu.2018.02485delete
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摘要

摘要

En 中文
Immunotherapy is revolutionizing health care, with the majority of high impact drugs approved in the past decade falling into this category of therapy. Despite considerable success, glycosylation-a key design parameter that ensures safety, optimizes biological response, and influences the pharmacokinetic properties of an immunotherapeutic-has slowed the development of this class of drugs in the past and remains challenging at present. This article describes how optimizing glycosylation through a variety of glycoengineering strategies provides enticing opportunities to not only avoid past pitfalls, but also to substantially improve immunotherapies including antibodies and recombinant proteins, and cell-based therapies. We cover design principles important for early stage pre-clinical development and also discuss how various glycoengineering strategies can augment the biomanufacturing process to ensure the overall effectiveness of immunotherapeutics.
Keyword:
immunotherapy
glycosylation
antibody-drug conjugates (ADCs)
monoclonal antibodies
antibodydependent cell cytotoxicity (ADCC)
glycoengineering
metabolic glycoengineering
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期刊

Frontiers in Immunology 封面图
Frontiers in Immunology
IF:
5.9
论文数:
5.0W
被引数:
22.7W

机构

J
Johns Hopkins University
学者数:
10.2W
论文数: 8.8W
被引数: 13.0W
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