Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Mar;18(3):335-50.
doi: 10.1517/14728222.2014.877891.

Targeting the Fc receptor in autoimmune disease

Affiliations
Review

Targeting the Fc receptor in autoimmune disease

Xinrui Li et al. Expert Opin Ther Targets. 2014 Mar.

Abstract

Introduction: The Fc receptors (FcRs) and their interactions with immunoglobulin and innate immune opsonins, such as C-reactive protein, are key players in humoral and cellular immune responses. As the effector mechanism for some therapeutic monoclonal antibodies, and often a contributor to the pathogenesis and progression of autoimmunity, FcRs are promising targets for treating autoimmune diseases.

Areas covered: This review discusses the nature of different FcRs and the various mechanisms of their involvement in initiating and modulating immunocyte functions and their biological consequences. It describes a range of current strategies in targeting FcRs and manipulating their interaction with specific ligands, while presenting the pros and cons of these approaches. This review also discusses potential new strategies including regulation of FcR expression and receptor crosstalk.

Expert opinion: FcRs are appealing targets in the treatment of inflammatory autoimmune diseases. However, there are still knowledge limitations and technical challenges, the most important being a better understanding of the individual roles of each of the FcRs and enhancement of the specificity in targeting particular cell types and specific FcRs.

PubMed Disclaimer

Conflict of interest statement

Declaration of interest.

The authors state no conflict of interest and have received no payment in preparation of this manuscript.

Figures

Figure 1
Figure 1
Structure of human classical Fc Receptors

References

    1. Marmont AM. Defining criteria for autoimmune diseases. Immunol Today. 1994;15(8):388. - PubMed
    1. Nimmerjahn F, Ravetch JV. Fc-receptors as regulators of immunity. Adv Immunol. 2007;96:179–204. ** A comprehensive review on types of Fc receptors, their signaling and functions.

    1. Ernst LK, van de Winkel JG, Chiu IM, et al. Three genes for the human high affinity Fc receptor for IgG (Fc gamma RI) encode four distinct transcription products. J Biol Chem. 1992;267(22):15692–15700. - PubMed
    1. Hoffmeyer F, Witte K, Schmidt RE. The high-affinity Fc gamma RI on PMN: regulation of expression and signal transduction. Immunology. 1997;92(4):544–552. - PMC - PubMed
    1. Capel PJ, van de Winkel JG, van den Herik-Oudijk IE, et al. Heterogeneity of human IgG Fc receptors. Immunomethods. 1994;4(1):25–34. - PubMed

Publication types