Bordron A, Charras A, Le Dantec C, Renaudineau Y
Inserm U1227, lymphocytes B et auto-immunité, institut Brest santé agro-matière, labex IGO, REPICGO network, université de Brest, 29609 Brest, France.
Inserm U1227, lymphocytes B et auto-immunité, institut Brest santé agro-matière, labex IGO, REPICGO network, université de Brest, 29609 Brest, France; Laboratoire d'immunologie et immunothérapie, CHRU Morvan, 29609 Brest cedex, France.
Rev Med Interne. 2018 May;39(5):346-351. doi: 10.1016/j.revmed.2017.09.003. Epub 2017 Oct 18.
Sjögren's syndrome (SS) is a systemic autoimmune epithelitis with a major female incidence, and characterized by a dry syndrome, impaired quality of life, visceral involvement, and lymphoma for the most aggressive cases. During this process, epithelial cells acquire the capacity to produce cytokines, chemokines, and autoantigens which can in turn be presented to the immune system. Consequently, this epithelitis is accompanied by lymphocytic infiltrations leading to the formation of pseudo-follicles in which self-reactive B lymphocytes are present. The recent integration of genomic and especially of epigenomic data, which make it possible to analyze the different cellular partners, opens new perspectives and allows to a better understanding of this complex and still incurable disease.
干燥综合征(SS)是一种主要发生于女性的系统性自身免疫性上皮炎,其特征为干燥综合征、生活质量受损、内脏受累,最严重的病例会发展为淋巴瘤。在此过程中,上皮细胞获得产生细胞因子、趋化因子和自身抗原的能力,而这些物质又可呈递给免疫系统。因此,这种上皮炎伴有淋巴细胞浸润,导致假性滤泡形成,其中存在自身反应性B淋巴细胞。基因组数据尤其是表观基因组数据的最新整合,使得分析不同细胞成分成为可能,这为深入了解这种复杂且仍无法治愈的疾病开辟了新的视角。