Center for Autoimmune Liver Diseases, Humanitas Clinical and Research Center, Rozzano, MI, Italy.
J Autoimmun. 2013 Mar;41:87-91. doi: 10.1016/j.jaut.2012.12.008. Epub 2013 Feb 1.
Sex chromosome abnormalities have been advocated to be involved in the striking female prevalence of primary biliary cirrhosis (PBC) and women with PBC manifest an increased X chromosome loss in peripheral blood mononuclear cells compared to age-matched healthy women. Our knowledge of the etiopathogenesis of autoimmunity in male patients remains, however, limited. Next to the possible role of androgens and their imbalances, the Y chromosome appears as a potential candidate for influence of the immune function in men. Herein we analyzed a population of male patients with primary biliary cirrhosis (n = 26) and healthy controls (n = 88) to define a potential association of disease and the loss of the Y chromosome. We demonstrate that Y chromosome loss indeed is higher in PBC males compared to healthy controls, and this phenomenon increases with aging. We were, thus, able to confirm the existence of an analogous mechanism in the male population to previously identified X haploinsufficiency in female patients with organ-specific autoimmune disease. We propose that this commonality might represent a relevant feature in the etiopathogenesis of autoimmune diseases that should be further investigated.
性染色体异常被认为与原发性胆汁性肝硬化(PBC)的女性高发有关,与年龄匹配的健康女性相比,PBC 女性在外周血单核细胞中表现出 X 染色体丢失增加。然而,我们对男性自身免疫患者的发病机制的了解仍然有限。除了雄激素及其失衡的可能作用外,Y 染色体似乎是影响男性免疫功能的潜在候选者。在此,我们分析了一组原发性胆汁性肝硬化男性患者(n=26)和健康对照(n=88),以确定疾病与 Y 染色体丢失之间的潜在关联。我们证明,与健康对照组相比,PBC 男性的 Y 染色体丢失确实更高,并且这种现象随着年龄的增长而增加。因此,我们能够证实,在男性人群中存在与先前在女性器官特异性自身免疫性疾病患者中鉴定出的 X 染色体单倍体不足类似的机制。我们提出,这种共性可能是自身免疫性疾病发病机制中的一个重要特征,值得进一步研究。