Seitzer U, Swider C, Stüber F, Suchnicki K, Lange A, Richter E, Zabel P, Müller-Quernheim J, Flad H D, Gerdes J
Forschungszentrum Borstel, Parkallee 22, Borstel, D-23845, Germany.
Cytokine. 1997 Oct;9(10):787-90. doi: 10.1006/cyto.1997.0224.
Biallelic polymorphisms in the promoter region of the TNF-alpha gene (TNFA) and in the first intron of the TNF-beta gene (TNFB) have been associated with variation in TNF-alpha production and with susceptibility to severe diseases. Among other functions, TNF-alpha plays a pivotal role in regulatory aspects of granuloma formation and sustenance. In sarcoidosis, a systemic granulomatous disorder of unknown aetiology, the clinical course of the disease has been associated with the patient's individual capacity of spontaneous TNF-alpha production by alveolar macrophages. We determined the TNFA and TNFB polymorphisms in 101 patients with pulmonary sarcoidosis and 216 healthy blood donors. A highly significant shift to the more uncommon TNFA2 allele was found in the Löfgren syndrome patient group, which represents the acute form of the disease with frequent spontaneous remission. The results show that gene frequencies of the TNFA gene variation are significantly different within the clinical forms of sarcoidosis, indicating that genetic predisposition for TNF-alpha production may play a role in the pathogenesis of the disease.
肿瘤坏死因子-α基因(TNFA)启动子区域和肿瘤坏死因子-β基因(TNFB)第一内含子中的双等位基因多态性与肿瘤坏死因子-α产生的变化以及对严重疾病的易感性有关。在其他功能中,肿瘤坏死因子-α在肉芽肿形成和维持的调节方面起着关键作用。在结节病(一种病因不明的全身性肉芽肿性疾病)中,疾病的临床过程与患者肺泡巨噬细胞自发产生肿瘤坏死因子-α的个体能力有关。我们测定了101例肺结节病患者和216名健康献血者的TNFA和TNFB多态性。在 Löfgren 综合征患者组中发现向更罕见的TNFA2等位基因有高度显著的偏移,Löfgren 综合征代表疾病的急性形式,常自发缓解。结果表明,结节病临床类型中TNFA基因变异的基因频率存在显著差异,这表明肿瘤坏死因子-α产生的遗传易感性可能在疾病发病机制中起作用。