Silvennoinen-Kassinen S, Ikäheimo I, Tiilikainen A
Department of Medical Microbiology, University of Oulu, Finland.
Int Arch Allergy Immunol. 1997 Sep;114(1):94-6. doi: 10.1159/000237650.
The study was undertaken to see whether TAP1 and TAP2 (transporter associated with antigen processing) genes are involved in susceptibility to nickel allergy. The products of these genes are important in antigen transport and processing, making them candidates for disease susceptibility. Fifty-five nickel-sensitive and 54 non-sensitive subjects were TAP1- and TAP2-typed by amplification refractory mutation system - polymerase chain reaction. The allele and phenotype frequencies of TAP2B were significantly (p = 0.019 and 0.012, respectively) increased in nickel-sensitive subjects versus controls. Relative risk (RR) for TAP2B was 2.7 and etiological factor (EF) = 0.46. The allele frequency of TAP2C was decreased among the nickel-sensitive subjects versus controls (p = 0.016). RR for TAP2C was 0.18. In conclusion, TAP2B increases the risk for nickel allergy, the results suggesting a considerably high EF.
开展这项研究是为了观察TAP1和TAP2(抗原加工相关转运体)基因是否与镍过敏易感性有关。这些基因的产物在抗原运输和加工过程中起重要作用,使其成为疾病易感性的候选因素。通过扩增阻滞突变系统-聚合酶链反应对55名对镍敏感和54名对镍不敏感的受试者进行TAP1和TAP2分型。与对照组相比,镍敏感受试者中TAP2B的等位基因和表型频率显著增加(分别为p = 0.019和0.012)。TAP2B的相对风险(RR)为2.7,病因学因素(EF)= 0.46。与对照组相比,镍敏感受试者中TAP2C的等位基因频率降低(p = 0.016)。TAP2C的RR为0.18。总之,TAP2B增加了镍过敏的风险,结果表明病因学因素相当高。