Gottenberg Jacques-Eric, Cagnard Nicolas, Lucchesi Carlo, Letourneur Franck, Mistou Sylvie, Lazure Thierry, Jacques Sebastien, Ba Nathalie, Ittah Marc, Lepajolec Christine, Labetoulle Marc, Ardizzone Marc, Sibilia Jean, Fournier Catherine, Chiocchia Gilles, Mariette Xavier
Institut Pour la Santé et de la Recherche Médicale E 802 and Service de Rhumatologie, Hôpital de Bicêtre, Assistance Publique-Hôpitaux de Paris, 94275 Le Kremlin Bicêtre, France.
Proc Natl Acad Sci U S A. 2006 Feb 21;103(8):2770-5. doi: 10.1073/pnas.0510837103. Epub 2006 Feb 13.
Gene expression analysis of target organs might help provide new insights into the pathogenesis of autoimmune diseases. We used global gene expression profiling of minor salivary glands to identify patterns of gene expression in patients with primary Sjögren's syndrome (pSS), a common and prototypic systemic autoimmune disease. Gene expression analysis allowed for differentiating most patients with pSS from controls. The expression of 23 genes in the IFN pathways, including two Toll-like receptors (TLR8 and TLR9), was significantly different between patients and controls. Furthermore, the increased expression of IFN-inducible genes, BAFF and IFN-induced transmembrane protein 1, was also demonstrated in ocular epithelial cells by quantitative RT-PCR. In vitro activation showed that these genes were effectively modulated by IFNs in salivary gland epithelial cells, the target cells of autoimmunity in pSS. The activation of IFN pathways led us to investigate whether plasmacytoid dendritic cells were recruited in salivary glands. These IFN-producing cells were detected by immunohistochemistry in all patients with pSS, whereas none was observed in controls. In conclusion, our results support the pathogenic interaction between the innate and adaptive immune system in pSS. The persistence of the IFN signature might be related to a vicious circle, in which the environment interacts with genetic factors to drive the stimulation of salivary TLRs.
对靶器官进行基因表达分析可能有助于为自身免疫性疾病的发病机制提供新的见解。我们利用小唾液腺的全基因表达谱来确定原发性干燥综合征(pSS)患者的基因表达模式,pSS是一种常见的典型系统性自身免疫性疾病。基因表达分析能够区分大多数pSS患者与对照组。患者与对照组之间,包括两种Toll样受体(TLR8和TLR9)在内的23种IFN通路相关基因的表达存在显著差异。此外,通过定量RT-PCR还证实了眼上皮细胞中IFN诱导基因、BAFF和IFN诱导跨膜蛋白1的表达增加。体外激活实验表明,在pSS自身免疫的靶细胞——唾液腺上皮细胞中,这些基因受到IFN的有效调控。IFN通路的激活促使我们研究浆细胞样树突状细胞是否在唾液腺中被募集。通过免疫组化在所有pSS患者中均检测到了这些产生IFN的细胞,而在对照组中未观察到。总之,我们的结果支持了pSS中固有免疫系统与适应性免疫系统之间的致病相互作用。IFN特征的持续存在可能与一个恶性循环有关,即环境与遗传因素相互作用,驱动唾液TLR的刺激。