Abstract

Antibodies participate in defense of the organism from all types of pathogens, including viruses, bacteria, fungi, and protozoa. IgG antibodies recognize their associated antigen via their two Fab portions and are in turn recognized though their Fc portion by specific Fcγ receptors (FcγRs) on the membrane of immune cells. Multiple types and polymorphic variants of FcγR exist. These receptors are expressed in many cells types and are also redundant in inducing cell responses. Crosslinking of FcγR on the surface of leukocytes activates several effector functions aimed toward the destruction of pathogens and the induction of an inflammatory response. In the past few years, new evidence on how the particular IgG subclass and the glycosylation pattern of the antibody modulate the IgG–FcγR interaction has been presented. Despite these advances, our knowledge of what particular effector function is activated in a certain cell and in response to a specific type of FcγR remains very limited today. On one hand, each immune cell could be programmed to perform a particular cell function after FcγR crosslinking. On the other, each FcγR could activate a particular signaling pathway leading to a unique cell response. In this review, I describe the main types of FcγRs and our current view of how particular FcγRs activate various signaling pathways to promote unique leukocyte functions.

Highlights

  • The first antibodies produced by the adaptive immune response belong to the immunoglobulin M (IgM) class

  • FcγRIIIb NA1 has been associated to Wegener granulomatosis [61] and systemic vasculitis [62], while FcγRIIIb NA2 has been associated to systemic lupus erythematosus (SLE) in Japanese people [54]

  • No specific changes in the number of NK cells expressing FcγRIIIa were found in this study, recently it has been proposed that NK cell activation during human immunodeficiency virus (HIV) infection leads to profound decreases in FcγRIIIa expression on NK cells [112]. These results suggest that NK cell activation-induced Fcγ receptors (FcγRs) cleavage may result in the soluble FcγRIII that associates with HIV disease progression, further suggesting a linkage between chronic NK cell activation and HIV disease progression [112]

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Summary

Carlos Rosales*

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, Mexico. Crosslinking of FcγR on the surface of leukocytes activates several effector functions aimed toward the destruction of pathogens and the induction of an inflammatory response. In the past few years, new evidence on how the particular IgG subclass and the glycosylation pattern of the antibody modulate the IgG–FcγR interaction has been presented. Despite these advances, our knowledge of what particular effector function is activated in a certain cell and in response to a specific type of FcγR remains very limited today. I describe the main types of FcγRs and our current view of how particular FcγRs activate various signaling pathways to promote unique leukocyte functions

INTRODUCTION
Each FcγR Activates Distinct Functions
Fcγ RECEPTORS
Polymorphisms and Links to Disease Susceptibility
Cell Expression of FcγRs
FcγRI FcγRIIa FcγRIIb FcγRIIIa
IgG BINDING AFFINITY FOR FcγRs
The Role of Particular IgG Subclass
IgG subclass
The Role of Antibody Glycosylation Pattern
Fc RECEPTOR SIGNALING
EACH FcγR LEADS TO UNIQUE CELLULAR RESPONSES
CONCLUSION
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