| Literature DB >> 25488117 |
Ditza Levin1, Basil Golding2, Scott E Strome3, Zuben E Sauna4.
Abstract
The platform technology of fragment crystallizable (Fc) fusion, in which the Fc region of an antibody is genetically linked to an active protein drug, is among the most successful of a new generation of bioengineering strategies. Immunogenicity is a critical safety concern in the development of any protein therapeutic. While the therapeutic goal of generating Fc-fusion proteins has been to extend half-life, there is a critical mass of literature from immunology indicating that appropriate design of the Fc component has the potential to engage the immune system for product-specific outcomes. In the context of Fc-fusion therapeutics, a review of progress in understanding Fc biology suggests the prospect of engineering products that have an extended half-life and are able to modulate the immune system. Published by Elsevier Ltd.Keywords: Fc receptors; Fc-fusion technology; drug development; immunogenicity; neutralizing antidrug antibodies; therapeutic proteins
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Year: 2014 PMID: 25488117 DOI: 10.1016/j.tibtech.2014.11.001
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536