Effective Phagocytosis of Low Her2 Tumor Cell Lines with Engineered, Aglycosylated IgG Displaying High FcγRIIa Affinity and Selectivity-Reference-Cited by-同舟云学术

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Effective Phagocytosis of Low Her2 Tumor Cell Lines with Engineered, Aglycosylated IgG Displaying High FcγRIIa Affinity and Selectivity

Published:2012-10-11 Issue:2 Volume:8 Page:368-375
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Jung Sang Taek¹,Kelton William,Kang Tae Hyun,Ng Daphne T.W.,Andersen Jan Terje²³,Sandlie Inger²³,Sarkar Casim A.,Georgiou George

Affiliation:

1. Department of Bio and Nano Chemistry, Kookmin University, Seoul, Republic of Korea

2. Centre for Immune Regulation (CIR) and Department of Molecular Biosciences, University of Oslo, 0316 Oslo, Norway

3. CIR and Department of Immunology, Rikshospitalet University Hospital, N-0424 Oslo, Norway

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cb300455f

Reference40 articles.

1. Antibody-mediated modulation of immune responses

2. FcγRIIB in autoimmunity and infection: evolutionary and therapeutic implications

3. Specificity and affinity of human Fcγ receptors and their polymorphic variants for human IgG subclasses

4. Engineered antibody Fc variants with enhanced effector function

5. Fc Optimization of Therapeutic Antibodies Enhances Their Ability to Kill Tumor Cells In vitro and Controls Tumor Expansion In vivo via Low-Affinity Activating Fcγ Receptors

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