Wu Jianming, Lin Rui, Huang Jinhai, Guan Weihua, Oetting William S, Sriramarao P, Blumenthal Malcolm N
Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America ; Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America.
Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America.
PLoS One. 2014 Feb 21;9(2):e89196. doi: 10.1371/journal.pone.0089196. eCollection 2014.
IgG Fc receptors (FcγRs) play important roles in immune responses. It is not clear whether FcγR receptors play a role in human asthma and allergy. The aim of current study was to investigate whether functional single nucleotide polymorphisms (SNPs) of FcγR genes (FCGR) are associated with human asthma and allergy.
Functional SNPs of FCGR2A (FcγRIIA-131His>Arg, rs1801274), FCGR2B (FcγRIIB-187Ile>Thr, rs1050501), FCGR2C (FcγRIIC-13Gln>Stop, rs10917661), FCGR3A (FcγRIIIA-158Val>Phe, rs396991), and FCGR3B variants (FcγRIIIB NA1 and NA2) were genotyped in an asthma family cohort including 370 atopy positive, 239 atopy negative, and 169 asthma positive subjects. The genotype and phenotype data (asthma, bronchial hyper-responsiveness, and atopy) of subjects were analyzed using family-based association tests (FBAT) and logistic regression adjusted for age and sex.
The FcγRIIA-131His>Arg SNP is significantly associated with atopy in a family-based association test (P = 0.00287) and in a logistic regression analysis (P = 0.0269, OR 0.732, 95% CI: 0.555-0.965). The FcγRIIA-131His (or rs1801274-A) allele capable of binding human IgG2 has a protective role against atopy. In addition, the rare FcγRIIB-187Thr (or rs1050501-C) allele defective for the receptor-mediated inhibitory signals is a risk factor for atopy (P = 0.0031, OR 1.758, 95% CI: 1.209-2.556) and IgE production (P<0.001). However, variants of activating FcγRIIIA (rs396991), and FcγRIIIB (NA1 and NA2), and FcγRIIC (rs10917661) are not associated with asthma, BHR, and atopy (P>0.05).
FcγRIIA and FcγRIIB functional polymorphisms may have a role in the pathogenesis of allergy.
IgG Fc受体(FcγRs)在免疫反应中发挥重要作用。FcγR受体是否在人类哮喘和过敏中起作用尚不清楚。本研究的目的是调查FcγR基因(FCGR)的功能性单核苷酸多态性(SNPs)是否与人类哮喘和过敏相关。
对FCGR2A(FcγRIIA-131His>Arg,rs1801274)、FCGR2B(FcγRIIB-187Ile>Thr,rs1050501)、FCGR2C(FcγRIIC-13Gln>Stop,rs10917661)、FCGR3A(FcγRIIIA-158Val>Phe,rs396991)和FCGR3B变体(FcγRIIIB NA1和NA2)进行基因分型,该哮喘家系队列包括370例特应性阳性、239例特应性阴性和169例哮喘阳性受试者。使用基于家系的关联测试(FBAT)以及针对年龄和性别进行调整的逻辑回归分析受试者的基因型和表型数据(哮喘、支气管高反应性和特应性)。
在基于家系的关联测试(P = 0.00287)和逻辑回归分析(P = 0.0269,OR 0.732,95% CI:0.555 - 0.965)中,FcγRIIA-131His>Arg SNP与特应性显著相关。能够结合人IgG2的FcγRIIA-131His(或rs1801274-A)等位基因对特应性具有保护作用。此外,受体介导的抑制信号缺陷的罕见FcγRIIB-187Thr(或rs1050501-C)等位基因是特应性(P = 0.0031,OR 1.758,95% CI:1.209 - 2.556)和IgE产生(P<0.001)的危险因素。然而,激活型FcγRIIIA(rs396991)、FcγRIIIB(NA1和NA2)以及FcγRIIC(rs10917661)的变体与哮喘、支气管高反应性和特应性无关(P>0.05)。
FcγRIIA和FcγRIIB功能多态性可能在过敏发病机制中起作用。