Fc-Engineered Therapeutic Antibodies: Recent Advances and Future Directions.
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BORIS DOI
Date of Publication
September 28, 2023
Publication Type
Article
Contributor
Abdeldaim, Dalia T | |
Schindowski, Katharina |
Series
Pharmaceutics
ISSN or ISBN (if monograph)
1999-4923
Publisher
MDPI
Language
English
Publisher DOI
PubMed ID
37896162
Uncontrolled Keywords
Description
Monoclonal therapeutic antibodies have revolutionized the treatment of cancer and other diseases. Fc engineering aims to enhance the effector functions or half-life of therapeutic antibodies by modifying their Fc regions. Recent advances in the Fc engineering of modern therapeutic antibodies can be considered the next generation of antibody therapy. Various strategies are employed, including altering glycosylation patterns via glycoengineering and introducing mutations to the Fc region, thereby enhancing Fc receptor or complement interactions. Further, Fc engineering strategies enable the generation of bispecific IgG-based heterodimeric antibodies. As Fc engineering techniques continue to evolve, an expanding portfolio of Fc-engineered antibodies is advancing through clinical development, with several already approved for medical use. Despite the plethora of Fc-based mutations that have been analyzed in in vitro and in vivo models, we focus here in this review on the relevant Fc engineering strategies of approved therapeutic antibodies to finetune effector functions, to modify half-life and to stabilize asymmetric bispecific IgGs.
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File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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pharmaceutics-15-02402-v2.pdf | text | Adobe PDF | 1.75 MB | Attribution (CC BY 4.0) | published |