Division of Rheumatology, Clinical and Experimental Medicine, University of Padova, Padova, Italy.
Swiss Med Wkly. 2010 Apr 3;140(13-14):187-201. doi: 10.4414/smw.2010.12597.
During pregnancy the maternal immune system is modified in order to achieve immune tolerance toward paternal antigen expressed on foetal cells. These modifications, which occur both at the foeto-maternal interface and in the systemic circulation, are driven by oestrogens and progesterone whose blood concentrations increase during pregnancy. The cytokine profile is also modified. Th2 cytokines are enhanced while the Th1 response is inhibited. This could explain why Th1-mediated autoimmune diseases tend to improve and Th2-mediated diseases, such as systemic lupus erythematosus (SLE), tend to worsen during pregnancy. However, whether or not SLE relapses more frequently during pregnancy is still a matter of debate. Steroid hormone and cytokine profiles differ in SLE patients compared with healthy subjects during pregnancy leading to a dysregulation of the balance between cell-mediated and humoral immune response, which, in turn, could explain the variability of the SLE course during gestation. This review focuses on hormonal-related cytokine changes observed during pregnancy in healthy subjects and SLE patients.
在妊娠期间,母体免疫系统会发生改变,以实现对胎儿细胞上父系抗原的免疫耐受。这些改变发生在胎儿-母体界面和全身循环中,由雌激素和孕激素驱动,其血液浓度在妊娠期间增加。细胞因子谱也会发生改变。Th2 细胞因子增强,而 Th1 反应受到抑制。这可以解释为什么 Th1 介导的自身免疫性疾病往往会改善,而 Th2 介导的疾病,如系统性红斑狼疮 (SLE),在妊娠期间往往会恶化。然而,SLE 是否在妊娠期间更频繁地复发仍然存在争议。与健康受试者相比,SLE 患者在妊娠期间的类固醇激素和细胞因子谱存在差异,导致细胞介导和体液免疫反应之间的平衡失调,这反过来又可以解释 SLE 在妊娠期间的变化。这篇综述重点关注健康受试者和 SLE 患者在妊娠期间观察到的与激素相关的细胞因子变化。