Arthritis Research UK Centre for Adolescent Rheumatology at UCL, ULCH and GOSH, London, United Kingdom.
Division of Medicine, Centre for Rheumatology, UCL, London, United Kingdom.
Front Immunol. 2019 Jan 15;9:3167. doi: 10.3389/fimmu.2018.03167. eCollection 2018.
Type 1 interferons (IFN) are an antiviral cytokine family, important in juvenile onset systemic lupus erythematosus (jSLE) which is more common in females, around puberty. We report that plasmacytoid dendritic cells (pDC) from healthy females produced more type 1 IFN after toll like receptor (TLR) 7 signaling than males, even before puberty, but that puberty itself associated with increased production of type 1 IFN. A unique human model allows us to show that this was related to X chromosome number, and serum testosterone concentration, in a manner which differed depending on the number of X chromosomes present. In addition, we have showed that pDC were more activated in females overall, and immune cell gene expression was higher in females after puberty. Therefore, sex hormones and X chromosome number were associated individually and interactively with the type 1 IFN response, which contributes to our understanding of why females are more likely to develop an IFN mediated disease like jSLE after puberty.
1 型干扰素(IFN)是一种抗病毒细胞因子家族,在青少年发病的系统性红斑狼疮(jSLE)中很重要,jSLE 在女性中更为常见,通常发生在青春期前后。我们报告称,健康女性的浆细胞样树突状细胞(pDC)在 Toll 样受体(TLR)7 信号作用后产生的 1 型 IFN 多于男性,甚至在青春期之前,但青春期本身与 1 型 IFN 的产生增加有关。一个独特的人类模型使我们能够表明,这与 X 染色体数量和血清睾酮浓度有关,其方式因存在的 X 染色体数量而异。此外,我们还表明,pDC 在女性中总体上更为活跃,青春期后女性的免疫细胞基因表达更高。因此,性激素和 X 染色体数量单独和相互作用与 1 型 IFN 反应有关,这有助于我们理解为什么女性在青春期后更有可能患上 IFN 介导的疾病,如 jSLE。