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Improving Immunotherapy Through Glycodesign.
Buettner, Matthew J; Shah, Sagar R; Saeui, Christopher T; Ariss, Ryan; Yarema, Kevin J.
Afiliación
  • Buettner MJ; Department of Biomedical Engineering and the Translational Tissue Engineering Center, The Johns Hopkins University, Baltimore, MD, United States.
  • Shah SR; Department of Biomedical Engineering and the Translational Tissue Engineering Center, The Johns Hopkins University, Baltimore, MD, United States.
  • Saeui CT; Department of Biomedical Engineering and the Translational Tissue Engineering Center, The Johns Hopkins University, Baltimore, MD, United States.
  • Ariss R; Pharmacology/Toxicology Branch I, Division of Clinical Evaluation and Pharmacology/Toxicology, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Bethesda, MD, United States.
  • Yarema KJ; Department of Biomedical Engineering and the Translational Tissue Engineering Center, The Johns Hopkins University, Baltimore, MD, United States.
Front Immunol ; 9: 2485, 2018.
Article en En | MEDLINE | ID: mdl-30450094
ABSTRACT
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Productos Biológicos / Ingeniería Biomédica / Proteínas Recombinantes / Inmunoterapia / Anticuerpos Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Productos Biológicos / Ingeniería Biomédica / Proteínas Recombinantes / Inmunoterapia / Anticuerpos Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article