Kobayashi T, Westerdaal N A, Miyazaki A, van der Pol W L, Suzuki T, Yoshie H, van de Winkel J G, Hara K
Department of Periodontology, Niigata University School of Dentistry, Japan.
Infect Immun. 1997 Sep;65(9):3556-60. doi: 10.1128/iai.65.9.3556-3560.1997.
Polymorphonuclear neutrophil (PMN) phagocytic function has been shown to be impaired in some patients with periodontitis. PMN constitutively express members of two immunoglobulin G receptor (Fc gammaR) classes: Fc gammaRIIa (CD32) and Fc gammaRIIIb (CD16). Both receptors exhibit genetically determined structural and functional biallelic polymorphisms, which have been shown to influence PMN phagocytic function. In this study, we assessed the relevance of these Fc gammaR polymorphisms to susceptibility to adult periodontitis and recurrence rate. The distribution of Fc gammaRIIa and Fc gammaRIIIb genotypes of 100 Japanese patients with adult periodontitis during follow-up was compared to the distribution of genotypes in 105 race-matched healthy controls. No significant skewing of distributions of Fc gammaRIIa and Fc gammaRIIIb genotypes was observed between patients and controls. Notably, however, a significant overrepresentation of the Fc gammaRIIIb-NA2 allotype was found in patients with disease recurrence (P < 0.05; odds ratio, 4.29; 95% confidence interval, 1.19 to 16.24). Moreover, the annual rate of recurrence was significantly higher in patients with the Fc gammaRIIIb-NA2/NA2 and Fc gammaRIIIb-NA1/NA2 genotypes than in Fc gammaRIIIb-NA1/NA1 individuals (P < 0.05). Fc gammaRIIa-R/R131 individuals also exhibited higher recurrence rates, though the difference was not statistically significant (P = 0.06). These results suggest that the Fc gammaRIIIb-NA2 allotype represents a risk factor for recurrence of adult periodontitis.
多形核中性粒细胞(PMN)的吞噬功能在一些牙周炎患者中已被证明存在受损情况。PMN组成性表达两类免疫球蛋白G受体(FcγR)成员:FcγRIIa(CD32)和FcγRIIIb(CD16)。这两种受体均表现出由基因决定的结构和功能双等位基因多态性,已证明这些多态性会影响PMN的吞噬功能。在本研究中,我们评估了这些FcγR多态性与成人牙周炎易感性及复发率的相关性。将100名日本成人牙周炎患者在随访期间的FcγRIIa和FcγRIIIb基因型分布与105名种族匹配的健康对照者的基因型分布进行比较。在患者和对照者之间未观察到FcγRIIa和FcγRIIIb基因型分布的显著偏差。然而,值得注意的是,在疾病复发的患者中发现FcγRIIIb - NA2同种异型显著过度表达(P < 0.05;优势比,4.29;95%置信区间,1.19至16.24)。此外,FcγRIIIb - NA2/NA2和FcγRIIIb - NA1/NA2基因型患者的年复发率显著高于FcγRIIIb - NA1/NA1个体(P < 0.05)。FcγRIIa - R/R131个体也表现出较高的复发率,尽管差异无统计学意义(P = 0.06)。这些结果表明,FcγRIIIb - NA2同种异型是成人牙周炎复发的一个危险因素。