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Fc gamma receptor I (CD64), Fc gamma receptor II (CD32), Fc gamma receptor III (CD16) (FcγRI (CD64), FcγRII (CD32), FcγRIII (CD16))

Target
FcγRI (CD64), FcγRII (CD32), FcγRIII (CD16)
Molecular classification
Receptor, Immunoglobulin superfamily, Cell surface receptor
01

Overview

Fc gamma receptors (FcγRs) are a family of cell surface receptors that bind to the Fc region of immunoglobulin G (IgG) antibodies and play a central role in linking humoral and cellular immunity. The three main classes on antigen-presenting cells (APCs) are Fc gamma receptor I (FcγRI, CD64), Fc gamma receptor II (FcγRII, CD32), and Fc gamma receptor III (FcγRIII, CD16). They differ in their structure, affinity for IgG subclasses, and their intracellular signaling motifs, which can be activating (ITAM) or inhibitory (ITIM). These receptors mediate key immune functions such as phagocytosis, antigen presentation, ADCC, and regulation of cytokine secretion, and are implicated in both host defense and in the pathology of autoimmune and inflammatory diseases. Their genetic diversity and expression levels can affect susceptibility to disease and response to antibody therapies[1][2][5][7][9].

Other names
Fcγ receptorsFcγRCD64 (FcγRI)CD32 (FcγRII)CD16 (FcγRIII)Immunoglobulin gamma Fc receptor
02

Mechanism of action

Triggering phagocytosis via ITAM-mediated signaling Inducing ADCC via NK cell activation Modulating cytokine production and degranulation Inhibiting immune activation (for FcγRIIB via ITIM motif) Altering antibody effector function through Fc engineering

03

Biological functions

Immune responsePhagocytosisAntigen presentationAntibody-dependent cellular cytotoxicity (ADCC)Cytokine productionDegranulationOpsonization
04

Disease associations

Autoimmune diseaseInflammationInfectionCancerImmune complex–mediated diseaseOther (e.g., allergy, chronic inflammatory conditions)
05

Safety considerations

Risk of excessive inflammation or cytokine releaseImmune complex–mediated tissue damageOff-target cytotoxicity (e.g., via ADCC or ADCP)Reduced efficacy due to receptor polymorphisms or downregulationPossible contribution to autoimmunity
06

Interacting drugs

Monoclonal antibodies (e.g., rituximab, trastuzumab, alemtuzumab)

4 more in the full profile.

07

Biomarkers

Surface expression of CD64 (FcγRI), CD32 (FcγRII), or CD16 (FcγRIII) on leukocytesChanges in receptor genotype or polymorphism in autoimmune disease risk or monoclonal antibody responseUse in patient selection for antibody-based cancer therapies

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