Veltkamp M, Grutters J C, van Moorsel C H M, Ruven H J T, van den Bosch J M M
Heart Lung Centre Utrecht, the Netherlands.
Clin Exp Immunol. 2006 Aug;145(2):215-8. doi: 10.1111/j.1365-2249.2006.03127.x.
The aetiology of sarcoidosis, a systemic disorder characterized by the formation of non-caseating granulomas in variable organs, remains enigmatic. Clarification is hampered by heterogeneity in disease phenotypes and course, due partly to the influence of a variety of genetic and environmental factors. Multiple studies have pointed towards bacteria as possible causative agents. Toll-like receptors (TLR) are innate immunity receptors important in the immune response against pathogens. TLR-4, together with CD14 and MD-2, is an essential receptor for the recognition of lipopolysaccharide (LPS), unique to the cell wall of Gram-negative bacteria. Recently, an association between TLR-4 polymorphism Asp299Gly, leading to a change in the extracellular domain of the receptor and possible hyporesponsiveness to LPS, and a chronic course of sarcoidosis was found in German patients. In the present study this polymorphism was genotyped in 156 Dutch sarcoidosis patients and 200 healthy Dutch controls using dual-labelled fluorescent oligonucleotides. No differences were found in allelic distributions between patients and controls (P = 0.79) or within the different clinical entities of the sarcoidosis group (P = 0.44). Importantly, there were no differences between the Dutch and German sarcoidosis patients (P = 0.62). However, the allelic distribution of the Asp299Gly polymorphism differed significantly between both control groups (P = 0.04). This study highlights the importance of testing a reported gene association in a distinct population when performing genetic association studies.
结节病是一种全身性疾病,其特征是在不同器官中形成非干酪样肉芽肿,但其病因仍然不明。疾病表型和病程的异质性阻碍了病因的明确,部分原因是多种遗传和环境因素的影响。多项研究指出细菌可能是致病因素。Toll样受体(TLR)是先天免疫受体,在针对病原体的免疫反应中起重要作用。TLR-4与CD14和MD-2一起,是识别脂多糖(LPS)的必需受体,脂多糖是革兰氏阴性菌细胞壁特有的成分。最近,在德国患者中发现TLR-4基因多态性Asp299Gly(导致受体细胞外结构域发生变化并可能对LPS反应低下)与结节病的慢性病程之间存在关联。在本研究中,使用双标记荧光寡核苷酸对156例荷兰结节病患者和200例健康荷兰对照进行了该多态性的基因分型。患者和对照之间的等位基因分布没有差异(P = 0.79),结节病组不同临床实体之间也没有差异(P = 0.44)。重要的是,荷兰和德国结节病患者之间没有差异(P = 0.62)。然而,两个对照组之间Asp299Gly多态性的等位基因分布存在显著差异(P = 0.04)。这项研究强调了在进行基因关联研究时,在不同人群中测试已报道的基因关联的重要性。