Brazão Vânia, Kuehn Christian Collins, dos Santos Carla Domingues, da Costa Cássia Mariana Bronzon, Júnior José Clóvis do Prado, Carraro-Abrahão Ana Amélia
College of Pharmaceutical Sciences of Ribeirão Preto (FCFRP), University of São Paulo, Av. do Café s/n, 14040-903 Ribeirão Preto, São Paulo, Brazil.
College of Pharmaceutical Sciences of Ribeirão Preto (FCFRP), University of São Paulo, Av. do Café s/n, 14040-903 Ribeirão Preto, São Paulo, Brazil.
Immunobiology. 2015 Jan;220(1):42-7. doi: 10.1016/j.imbio.2014.09.005. Epub 2014 Sep 16.
Pregnancy is known to induce a transient depression of maternal cell-mediated immunity, to prevent rejection of the fetus, while at the same time it keeps adequate maternal host defense mechanisms to fight infection. Presently, the aim of this paper was to investigate a possible endocrine and immunologic alteration observed during a successful pregnancy. This study consistently showed that plasma corticosterone levels were significantly higher (P<0.0001) in pregnant Wistar rats than in virgin female. An increased number of peritoneal macrophages was also detected in pregnant females when compared to non-pregnant ones. Macrophages play an important role in the production of bioactive proteins and lipids such as nitric oxide. Then, in support of the latter, the present study showed increased levels of endogenous NO in pregnant rats when compared to non-pregnant ones, thereby mediating the vasodilatation process of normal gestation. Furthermore, our FACS analysis clearly indicated the correlation between reduced CD161 expression on NK cells (P<0.0001) in pregnant rats when compared to virgin females. It was found that pregnancy appears to be associated with depressed cell immunity, as evidenced by a significant inhibition of lymphocyte proliferation. Understanding the immunological paradox of maternal tolerance, as well as the hormonal modulation of the immune environment during pregnancy is essential for future studies to investigate the potential for these processes to be modulated by diet or effective therapeutics during pregnancy.
众所周知,怀孕会导致母体细胞介导的免疫功能暂时下降,以防止胎儿被排斥,同时保持足够的母体宿主防御机制来抵抗感染。目前,本文的目的是研究在成功怀孕过程中观察到的可能的内分泌和免疫改变。这项研究始终表明,怀孕的Wistar大鼠血浆皮质酮水平显著高于未孕雌性大鼠(P<0.0001)。与未孕雌性大鼠相比,怀孕雌性大鼠的腹膜巨噬细胞数量也有所增加。巨噬细胞在生物活性蛋白和脂质如一氧化氮的产生中起重要作用。因此,为支持后者,本研究表明,与未孕大鼠相比,怀孕大鼠体内内源性一氧化氮水平升高,从而介导正常妊娠的血管舒张过程。此外,我们的流式细胞术分析清楚地表明,与未孕雌性大鼠相比,怀孕大鼠NK细胞上CD161表达降低之间存在相关性(P<0.0001)。研究发现,怀孕似乎与细胞免疫抑制有关,淋巴细胞增殖受到显著抑制就是证明。了解母体耐受性的免疫悖论以及怀孕期间免疫环境的激素调节,对于未来研究这些过程在怀孕期间被饮食或有效治疗方法调节的可能性至关重要。