The FcγR family recognizes the Fc part of IgG and is divided into several main classes (FcγRI, FcγRII, and FcγRIII), consisting of activating and inhibitory receptors, which additionally differ in their affinities to IgG and are specific for the individual IgG subclasses.
Fc receptors are predominantly membrane-bound receptors for different immunoglobulin isotypes. All molecules except the FcRn receptor belong to the immunoglobulin superfamily (see FC receptors below). The name is based on the binding specificity of the receptors to a part of the C-terminus of an antibody (called Fc fragment crystallizable) and the constant region of an antibody. Fc receptors are glycosylated. They are found on the surface of phagocytes, B lymphocytes, NK cells and dendritic cells.
The biological activity of an IgG antibody (e.g. neutralization of viruses and bacterial toxins, mediation of an anti-tumour response) is determined by the relative affinity to the respective antigen and to the respective FcγR. Certain receptor variants (e.g. the high-affinity Val158-FcγRIIIa receptor variant) have been shown to respond better to rituximab antibody therapy in rheumatoid arthritis than other receptor variants (Ruyssen-Witrand A et al. 2012).