Recapitulation of IVIG Anti-Inflammatory Activity with a Recombinant IgG Fc
Scripps Research Institute · University of New Hampshire · +2 more institutions
Abstract
It is well established that high doses of monomeric immunoglobulin G (IgG) purified from pooled human plasma [intravenous immunoglobulin (IVIG)] confer anti-inflammatory activity in a variety of autoimmune settings. However, exactly how those effects are mediated is not clear because of the heterogeneity of IVIG. Recent studies have demonstrated that the anti-inflammatory activity of IgG is completely dependent on sialylation of the N-linked glycan of the IgG Fc fragment. Here we determine the precise glycan requirements for this anti-inflammatory activity, allowing us to engineer an appropriate IgG1 Fc fragment, and thus generate a fully recombinant, sialylated IgG1 Fc with greatly enhanced potency. This…
Citation impact
- FWCI
- 42.62
- Percentile
- 100%
- References
- 34
Authors
6- RMRobert M. AnthonyCorresponding
Scripps Research Institute, University of New Hampshire, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rockefeller University
- FNFalk Nimmerjahn
Scripps Research Institute, University of New Hampshire, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rockefeller University
- DJDavid J. Ashline
Scripps Research Institute, University of New Hampshire, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rockefeller University
- VNVernon N. Reinhold
Scripps Research Institute, University of New Hampshire, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rockefeller University
- JCJames C. Paulson
Scripps Research Institute, University of New Hampshire, Friedrich-Alexander-Universität Erlangen-Nürnberg, Rockefeller University
Topics & keywords
- Glycan
- Fragment crystallizable region
- Antibody
- Recombinant DNA
- Immunoglobulin G
- Potency
- Immunoglobulin superfamily
- Immunoglobulin E
- Good health and well-being