Invernizzi Pietro
Division of Internal Medicine and Liver Unit, San Paolo Hospital School of Medicine, University of Milan, Via di Rudinì 8, 20142 Milan, Italy.
Ann N Y Acad Sci. 2007 Sep;1110:57-64. doi: 10.1196/annals.1423.007.
Autoimmune diseases affect approximately 5% of the population in Western countries, with high female predominance. Family and twins studies have demonstrated that genetic factors are crucial determinants of susceptibility to autoimmune disease, but no specific genes have yet been identified. Recent studies indicate that X chromosome abnormalities, such as monosomy rates and inactivation patterns, occur in a number of female-predominant autoimmune diseases. We will review herein the most recent evidence on the role of the X chromosome in loss of tolerance and discuss its potential implications. Future studies will identify the X chromosome regions containing candidate genes for autoimmune susceptibility.
自身免疫性疾病影响着西方国家约5%的人口,女性患病率极高。家族研究和双胞胎研究表明,遗传因素是自身免疫性疾病易感性的关键决定因素,但尚未确定具体基因。最近的研究表明,X染色体异常,如单体率和失活模式,在许多女性主导的自身免疫性疾病中出现。我们将在此回顾关于X染色体在免疫耐受丧失中作用的最新证据,并讨论其潜在影响。未来的研究将确定包含自身免疫易感性候选基因的X染色体区域。