Kimura Tomomi, Saito Takafumi, Yoshimura Mika, Yixuan Song, Baba Masanori, Ji Guijin, Muramatsu Masaaki, Kawata Sumio
Department of Molecular Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
J Infect Dis. 2006 May 15;193(10):1371-4. doi: 10.1086/503436. Epub 2006 Apr 5.
Transforming growth factor (TGF)-beta 1 suppresses the proliferation and cytotoxicity of natural killer (NK) cells, which play critical roles in resolving hepatitis C virus (HCV) infection, especially during the acute phase. We examined 230 anti-HCV antibody-positive subjects for HCV RNA and the -509T/C genotype in the TGF-beta 1 gene promoter. The -509CC genotype and the -509C allele were significantly associated with higher HCV clearance rates (P=.01) and with lower transcriptional activity. The genetic effect remained significant even after adjustment for a history of transfusion. Low TGF- beta 1 producers might have less suppression of NK cells and be more likely to resolve HCV infection.
转化生长因子(TGF)-β1可抑制自然杀伤(NK)细胞的增殖和细胞毒性,而NK细胞在清除丙型肝炎病毒(HCV)感染中发挥关键作用,尤其是在急性期。我们检测了230名抗-HCV抗体阳性受试者的HCV RNA以及TGF-β1基因启动子中的-509T/C基因型。-509CC基因型和-509C等位基因与较高的HCV清除率显著相关(P = 0.01),且转录活性较低。即使在对输血史进行校正后,遗传效应仍很显著。低TGF-β1产生者对NK细胞的抑制作用可能较小,更有可能清除HCV感染。