Hwang Jung Hye, Kim Eun Joo, Koh Won-Jung, Kim Su Yeon, Lee Shin-Hye, Suh Gee Young, Kwon O Jung, Ki Chang Seok, Ji Yongick, Kang Miyeon, Kim Duk-Hwan
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
Tuberculosis (Edinb). 2007 Mar;87(2):166-71. doi: 10.1016/j.tube.2006.07.003. Epub 2006 Oct 4.
Interferon-gamma (IFN-gamma) is crucial for host defense against mycobacterial infections. Recent studies have indicated that IFN-gamma and IFN-gamma receptor 1 (IFN-gammaR1) gene polymorphisms are associated with susceptibility to pulmonary tuberculosis. The aim of this study was to test the hypothesis that IFN-gamma and IFN-gammaR1 gene polymorphisms influence susceptibility to lung disease caused by non-tuberculous mycobacteria (NTM). Seventy-six patients with the nodular bronchiectatic form of NTM lung disease (37 patients with Mycobacterium avium complex infection and 39 patients with Mycobacterium abscessus infection) and 80 controls were included. Polymorphisms of the IFN-gamma gene at position +874 were determined by the amplification refractory mutation system (ARMS) polymerase chain reaction assay and IFN-gammaR1 gene at positions -611, -270, -56 and +95 was genotyped by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry using genomic DNA. IFN-gammaR1 -270 and +95 polymorphisms were not present in any of the patients or controls. The patients with NTM lung disease showed no significant difference from controls in genotype and allele frequencies of the IFN-gamma +874 and IFN-gammaR1 -611 and -56 polymorphisms. The IFN-gamma +874 and IFN-gammaR1 -611 and -56 polymorphisms do not appear to be responsible for host susceptibility to NTM lung disease, at least in the Korean population.
干扰素-γ(IFN-γ)对于宿主抵御分枝杆菌感染至关重要。最近的研究表明,IFN-γ和干扰素-γ受体1(IFN-γR1)基因多态性与肺结核易感性相关。本研究的目的是检验以下假设:IFN-γ和IFN-γR1基因多态性会影响非结核分枝杆菌(NTM)所致肺部疾病的易感性。研究纳入了76例结节性支气管扩张型NTM肺病患者(37例鸟分枝杆菌复合群感染患者和39例脓肿分枝杆菌感染患者)以及80名对照者。采用扩增阻滞突变系统(ARMS)聚合酶链反应分析法测定IFN-γ基因+874位点的多态性,并使用基因组DNA通过基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱法对IFN-γR1基因-611、-270、-56和+95位点进行基因分型。在所有患者或对照者中均未发现IFN-γR1 -270和+95位点的多态性。NTM肺病患者在IFN-γ +874、IFN-γR1 -611和-56位点的基因型和等位基因频率与对照者相比无显著差异。至少在韩国人群中,IFN-γ +874、IFN-γR1 -611和-56位点的多态性似乎并非宿主对NTM肺病易感性的原因。