Department of Dermatology and Allergology, University of Szeged, Szeged, Hungary.
Hum Immunol. 2011 Oct;72(10):926-9. doi: 10.1016/j.humimm.2011.06.011. Epub 2011 Jul 1.
We aimed to study whether forkhead box P3 (FOXP3) polymorphisms contribute to allergic rhinitis (AR) in a Central-European population, the Hungarians, similarly as it was found in Han Chinese. A case-control study was performed and the genotype distribution of the rs3761548 FOXP3 polymorphism was analyzed separately in females and in males. The results demonstrated that females homozygous for the rare FOXP3 rs3761548 allele (A/A) are protected against AR; otherwise, females who are either wild types (C/C) or heterozygote carriers (C/A) of the rare allele are more susceptible to AR (OR [95%CI] = 2.089 [1,095; 3.988]). We were able to confirm the findings of Zhang et al. in a geographically and ethnically distinct population, the Hungarians, and revealed that the rs3761548 SNP is a marker of a haplotype in these two populations, but not in Sub-Saharan Africans, suggesting that this haplotype was fixed after early modern humans left Africa.
我们旨在研究叉头框蛋白 P3(FOXP3)多态性是否像在汉族人群中发现的那样,也导致中欧人群匈牙利人发生变应性鼻炎(AR)。进行了病例对照研究,并分别分析了女性和男性中 rs3761548 FOXP3 多态性的基因型分布。结果表明,罕见 FOXP3 rs3761548 等位基因(A/A)纯合的女性对 AR 有保护作用;相反,罕见等位基因(C/A)的野生型(C/C)或杂合子携带者(C/A)的女性更容易患 AR(OR [95%CI] = 2.089 [1,095; 3.988])。我们能够在地理位置和种族不同的人群匈牙利人中证实 Zhang 等人的发现,并揭示 rs3761548 SNP 是这两个人群中一个单倍型的标记,但不是撒哈拉以南非洲人群的标记,这表明该单倍型是在现代人离开非洲后固定下来的。