Objective. Several studies have recently identified polymorphisms of recept
ors for the Fc fragment of IgG (Fc gamma R) as genetic factors influencing
susceptibility to multiple autoimmune and infectious diseases. This genetic
predisposition could also influence the expression of Wegener's granulomat
osis (WG), a systemic autoimmune disease with chronic nasal carriage of Sta
phylococcus aureus as an important risk factor for disease relapses. Theref
ore, we analyzed 3 functional Fc gamma R polymorphisms from 91 patients wit
h WG and 154 controls for a possible relationship with disease expression a
nd occurrence of relapses.
Methods. Fc gamma R phenotypes were determined using amplification of Fc ga
mma R-genomic regions in allotype-specific polymerase chain reactions. Of p
articular interest in the analysis were 2 allotypic forms of Fc gamma RIIa
(R131 or H131) and 2 allotypic forms of Fc gamma RIIIa (V158 or F158), all
of which are functionally different.
Results. Analysis of Fc gamma R phenotypes demonstrated that patients with
WG were more prone to disease relapse in the first 5 years after diagnosis
if they were homozygous for both the R131 form of Fc gamma RIIa and the F15
8 form of Fc gamma RIIIa (relative risk 3,3, 95% confidence interval 1.6-6.
8). These polymorphisms are both associated with decreased FcR-mediated cle
arance, which may be relevant to the chronic nasal carriage of S aureus.
Conclusion. Both the R/H131 polymorphism of Fc gamma RIIa and the V/F158 po
lymorphism of Fc gamma RIIIa represent heritable risk factors for the devel
opment of disease relapses in WG.