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雌激素血清浓度会影响接受控制性卵巢刺激的女性血液免疫细胞组成和极化。

Estrogen serum concentration affects blood immune cell composition and polarization in human females under controlled ovarian stimulation.

机构信息

Department of Neurology, Institute of Neuroanatomy, Medical Clinic, RWTH Aachen University, 52074 Aachen, Germany.

Institute of Pharmacology and Toxicology, Medical Clinic, RWTH Aachen University, 52074 Aachen, Germany.

出版信息

J Steroid Biochem Mol Biol. 2018 Apr;178:340-347. doi: 10.1016/j.jsbmb.2018.02.005. Epub 2018 Feb 12.

Abstract

Estrogens modulate the immune system and possess anti-inflammatory properties. In line, immune cells express a variety of estrogen receptors (ER) including ER-alpha and -beta. In the present study, we examined the influence of 17beta-estradiol (E2) serum concentrations on blood leukocyte composition and their ex vivo polarization/activation status by FACS analysis in sub-fertile human females under controlled ovarian stimulation (COS). Using a set of cell-type and polarization-specific markers, we demonstrate that increased 17ß-estradiol (E2) serum concentrations yield an overall increase in leukocytes, neutrophils and monocytes but decreased lymphocytes. There was a clear ratio shift towards an increase in M2 monocytes with a protective quality and an increase in T-helper cells compared to a decrease in cytotoxic T-cells. These data support experimental findings and clinical trials, i.e. related to multiple sclerosis and other autoimmune-related diseases, that have shown a down-regulation of CD8(+) T cells and up-regulation of T-regulatory cells. Further studies have to pinpoint to which extent the immune system/-responsiveness of otherwise healthy female patients is affected by medium-term systemic E2 variations.

摘要

雌激素调节免疫系统并具有抗炎特性。相应地,免疫细胞表达多种雌激素受体(ER),包括 ER-α和 ER-β。在本研究中,我们通过流式细胞术分析,检查了在控制性卵巢刺激(COS)下,亚生育力的人类女性的血清中 17β-雌二醇(E2)浓度对白细胞组成及其体外极化/激活状态的影响。使用一组细胞类型和极化特异性标记物,我们证明了升高的 17β-雌二醇(E2)血清浓度导致白细胞、中性粒细胞和单核细胞总体增加,但淋巴细胞减少。M2 单核细胞的比例明显增加,具有保护作用,辅助性 T 细胞增加,而细胞毒性 T 细胞减少。这些数据支持实验发现和临床试验,即与多发性硬化症和其他自身免疫性相关疾病相关,这些研究表明 CD8+T 细胞下调和 T 调节细胞上调。进一步的研究必须确定在多大程度上,其他健康的女性患者的免疫系统/反应性受到中期系统性 E2 变化的影响。

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