Anti-inflammatory role of the IgA Fc receptor (CD89): From autoimmunity to therapeutic perspectives

作者:Ben Mkaddem Sanae; Rossato Elisabetta; Heming Nicholas; Monteiro Renato C*
来源:Autoimmunity Reviews, 2013, 12(6): 666-669.
DOI:10.1016/j.autrev.2012.10.011

摘要

The human immunoglobulin A (IgA) plays a key role in immune protection. IgA is the second most prevalent antibody in the serum. IgA-deficient patients frequently develop autoimmune or inflammatory diseases. The IgA function is mainly mediated through its interaction with the myeloid IgA Pc receptor Fc alpha RI (CD89). FcaRI, an immunoreceptor tyrosine-based activation motif (ITAM)-bearing receptor, has a dual function in immunity. Monovalent targeting of FcaRI, by anti-Fc alpha RI Fab or monomeric IgA, triggers potent inhibitory ITAM (ITAMi) signaling through the associated FcR gamma chain. This results in a low-intensity signaling cascade promoting recruitment of the tyrosine phosphatase SHP-1, which induces cell inhibition of multiple types of activation signals. In contrast, cross-linking of Fc alpha RI by multimeric ligand induces a high-intensity signaling pathway that leads to the recruitment of the tyrosine kinase Syk and to cell activation. Thus, Fc alpha RI acts as a regulator, which mediates both anti- and pro-inflammatory functions of IgA depending on the type of interaction. This balance is of great importance to prevent tissue damage in immunopathology and to ensure the return of activated cells to a resting state. The role of the IgA-Fc alpha RI interaction in the activation of different signaling pathways and its multifaceted role in immunity are discussed.

  • 出版日期2013-4