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Updated: Jan 28, 2026

Detection of True IgE-expressing Mouse B Lineage Cells
Published on: December 1, 2014
IgE Glycosylation in Health and Disease
Kai-Ting Shade1, Michelle E Conroy1, Robert M Anthony2
1Massachusetts General Hospital, Center for Immunology and Inflammatory Diseases, Harvard Medical School, 149 13th Street, Room 8.321, Boston, MA, 02129, USA.
Abstract:
IgE are absolutely required for initiation of allergy reactions, which affect over 20% of the world's population. IgE are the least prevalent immunoglobulins in circulation with 12-h and 2-day half-lives in mouse and human serum, respectively, but an extended tissue half-life of 3-weeks bound to the surface of mast cells by the high affinity IgE receptor, FcεRI (Gould and Sutton 2008). Although the importance of glycosylation to IgG biology is well established, less is known regarding the contribution of IgE glycosylation to allergic inflammation. IgE has seven and nine N-linked glycosylation sites distributed across human and murine constant chains, respectively. Here we discuss studies that have analyzed IgE glycosylation and its function, and how IgE glycosylation contributions to health and disease.
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