Chapter title |
IgA, IgA Receptors, and Their Anti-inflammatory Properties.
|
---|---|
Chapter number | 10 |
Book title |
Fc Receptors
|
Published in |
Current topics in microbiology and immunology, August 2014
|
DOI | 10.1007/978-3-319-07911-0_10 |
Pubmed ID | |
Book ISBNs |
978-3-31-907910-3, 978-3-31-907911-0
|
Authors |
Mkaddem SB, Christou I, Rossato E, Berthelot L, Lehuen A, Monteiro RC, Sanae Ben Mkaddem, Ivy Christou, Elisabetta Rossato, Laureline Berthelot, Agnès Lehuen, Renato C. Monteiro, Mkaddem, Sanae Ben, Christou, Ivy, Rossato, Elisabetta, Berthelot, Laureline, Lehuen, Agnès, Monteiro, Renato C. |
Abstract |
Immunoglobulin A (IgA) is the most abundantly produced antibody isotype in mammals. The primary function of IgA is to maintain homeostasis at mucosal surfaces and play a role in immune protection. IgA functions mainly through interaction with multiple receptors including IgA Fc receptor I (FcαRI), transferrin receptor 1 (CD71), asialoglycoprotein receptor (ASGPR), Fcα/μR, FcRL4, and DC-SIGN/SIGNR1. In this review we discuss recent data demonstrating anti-inflammatory functions of IgA through two receptors, the FcαRI and DC-SIGN/SIGNR1 interactions in the regulation of immunity. Serum monomeric IgA is able to mediate an inhibitory signal following the interaction with FcαRI. It results in partial phosphorylation of its FcRγ-ITAM and the recruitment of the tyrosine phosphatase SHP-1, which induces cell inhibition following the formation of intracellular clusters named inhibisomes. In contrast, cross-linking of FcαRI by multimeric ligands induces a full phosphorylation of the FcRγ-ITAM leading to the recruitment of the tyrosine kinase Syk and cell activation. In addition, secretory IgA can mediate a potent anti-inflammatory function following the sugar-dependent interaction with SIGNR1 on dendritic cells which induces an immune tolerance via regulatory T cell expansion. Overall, the anti-inflammatory effect of serum and secretory IgA plays a crucial role in the physiology and in the prevention of tissue damage in multiple autoimmune and inflammatory diseases. |
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