Carrozzo Marco, Dametto Ennia, Fasano Maria Edvige, Arduino Paolo, Bertolusso Giorgio, Uboldi de Capei Federica, Rendine Sabina, Amoroso Antonio
Department of Biomedical Sciences and Human Oncology, Oral Medicine Section, University of Turin, Turin, Italy.
Exp Dermatol. 2007 Sep;16(9):730-6. doi: 10.1111/j.1600-0625.2007.00577.x.
Cytokine polymorphisms may influence both the risk of developing oral lichen planus (OLP) and the outcome of hepatitis C virus (HCV)-infected patients and OLP has been frequently associated with HCV infection. The aim of the present study was to analyse whether cytokine polymorphisms may influence the susceptibility to HCV-related OLP. Thirty-five patients with OLP and chronic HCV infection (OLP-HCV+ve) took part in the study. As controls, 44 patients with OLP but without HCV (OLP-HCV-ve) infection and 140 healthy donors were studied. Thirteen cytokine genes with 22 single nucleotide polymorphisms (SNP) were studied. IFN-gamma UTR 5644 genotype frequencies showed an increase in number of A/T heterozygote in OLP-HCV+ve patients compared with OLP-HCV-ve that approached the statistical significance [P = 0.03, P-corrected (PC) = 0.66]. Contrarily, in OLP-HCV+ve patients, the frequency of genotype -308 G/A of the TNF-alpha was decreased, whereas the genotype -308 G/G was increased compared with OLP-HCV-ve (P = 0.0005, PC = 0.011 and P = 0.0016, PC = 0.0352, respectively). OLP patients with and without HCV infection showed a different genetic cytokine background suggesting distinct pathogenetic mechanisms.
细胞因子多态性可能既影响患口腔扁平苔藓(OLP)的风险,也影响丙型肝炎病毒(HCV)感染患者的病情转归,并且OLP常与HCV感染相关。本研究的目的是分析细胞因子多态性是否会影响对HCV相关OLP的易感性。35例OLP合并慢性HCV感染(OLP-HCV阳性)患者参与了本研究。作为对照,研究了44例OLP但未感染HCV(OLP-HCV阴性)的患者和140名健康供者。研究了13个细胞因子基因的22个单核苷酸多态性(SNP)。与OLP-HCV阴性患者相比,OLP-HCV阳性患者中IFN-γUTR 5644基因型频率显示A/T杂合子数量增加,接近统计学意义[P = 0.03,校正P值(PC)= 0.66]。相反,在OLP-HCV阳性患者中,与OLP-HCV阴性患者相比,TNF-α基因-308 G/A基因型频率降低,而-308 G/G基因型频率增加(分别为P = 0.0005,PC = 0.011和P = 0.0016,PC = 0.0352)。感染和未感染HCV的OLP患者显示出不同的细胞因子遗传背景,提示不同的发病机制。