articleJournal of Biological ChemistryJun 23, 2006HYBRID OA

Properties of Human IgG1s Engineered for Enhanced Binding to the Neonatal Fc Receptor (FcRn)

AstraZeneca (Germany)

PubMed
Indexed incrossrefdoajpubmed

Abstract

We describe here the functional implications of an increase in IgG binding to the neonatal Fc receptor. We have defined in a systematic fashion the relationship between enhanced FcRn binding of a humanized anti-respiratory syncytial virus (RSV) monoclonal antibody (MEDI-524) and the corresponding biological consequences in cynomolgus monkeys. The triple mutation M252Y/S254T/T256E (YTE) was introduced into the Fc portion of MEDI-524. Whereas these substitutions did not affect the ability of MEDI-524 to bind to its cognate antigen and inhibit RSV replication, they resulted in a 10-fold increase in its binding to both cynomolgus monkey and human FcRn at pH 6.0. MEDI-524-YTE was efficiently released from FcRn at…

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634
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Authors

3

Topics & keywords

Keywords
  • Neonatal Fc receptor
  • Antibody
  • Antibody-dependent cell-mediated cytotoxicity
  • Cytotoxicity
  • Monoclonal antibody
  • Receptor
  • Biology
  • Cell biology
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