紧急和早产孕妇免疫活性血细胞线粒体变化的复杂估计

S. Suprun, N. Kuderova, E. Suprun, O. Morozova, G. Evseeva, O. Lebedko
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引用次数: 0

摘要

炎症是促进胎膜早破(PPROM)发展的因素之一。在妊娠期生理免疫失衡的情况下,炎症改变其进程,甚至可以改变免疫反应。适当的指标可以是定量的和功能性的。我们使用线粒体膜电位标记物(MPM, Ay)作为衡量159名妊娠8-14周妇女免疫活性血细胞(IBC)功能状态的综合指标;观察至34-36周。在这些队列中,121名妇女被转介到对照组。主要组(n = 46)为28-33周PPROM孕妇。检查是在知情同意的情况下,按照现行医疗标准进行的,并得到远东呼吸生理学和病理学科学中心-妇幼保护研究所哈巴罗夫斯克分院伦理委员会的批准。此外,流式细胞术检测MPM和淋巴细胞群。IBC能量供应紊乱程度是基于MPM值降低的淋巴细胞、粒细胞和单核细胞数量同时测定的数据(申请发明号2020115963),从而揭示出3个程度的能量不足:1度,单变IBC组成,MPM降低;二度,双变成分,三度,总变化。PPROM孕妇CD3 (72% vs 78%, 1624 vs 1980), CD8 (28% vs 33%, 651 vs 851), CD19 (14% vs 9%, 304 vs 219)的相对和绝对下降。当评估IBC人群的MPM值时,发现由于第三度能量缺乏(从17%到26%),从妊娠1至2个月无能量缺乏的妇女比例下降(从41%到30%)。发现受影响的池在二级能量缺乏时有利于淋巴细胞-粒细胞关联(从7%到25%),从淋巴细胞-单核细胞室(从73%到50%)。从妊娠2 - 3个月,我们发现粒细胞池的重新分布在1级(0 - 8%),从淋巴细胞-粒细胞关联(25%和5%)到单核细胞-粒细胞关联(25%和40%)。在PPROM组中,由于3度能量缺乏(61%和26%),与对照组相比,无能量缺乏的孕妇比例(13%和27%)以及1度和2度(17%对31%和9%对17%)的孕妇比例有所下降。主组的IBC池在第1度重新分布,有利于粒细胞(25%和8%),在第2度,有利于淋巴细胞-单核细胞的关联(100%和55%),而不是粒细胞-单核细胞(0%和40%)。IBC中这种生物能量过程的不平衡可能是病理性持续炎症的重要因素。这些变化可能是由这类患者较高的感染发生率和母亲与胎儿之间的同种免疫相互作用引起的。然而,它们也可能决定炎症的病理过程。早产通常是由PPROM引起的,是一种多因素的病理状况。然而,独立于特定的触发因素,至少IBC能量供应的变化可以作为该疾病可能性的重要生物标志物。
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Complex estimation of mitochondrial changes of immunocompetent blood cells in pregnant women with urgent and premature birth
Inflammation is among the factors promoting development of premature rupture of the membranes (PPROM). Upon the conditions of physiological immune imbalance in pregnancy, inflammation modifies its course and can even change the immune response. Appropriate indexes may be quantitative and functional. We used a marker of mitochondrial membrane potential (MPM, Ay) as an integral index of the functional state of immunocompetent blood cells (IBC) in 159 women who were examined at 8-14 weeks of gestation; they were observed up to 34-36 weeks. Of these cohort, 121 women were referred to a comparison group. The main group (n = 46) consisted of pregnant women with PPROM at the term of 28-33 weeks. The examination was carried out according to current medical standards, with informed consent, being approved by the Ethics committee at the Khabarovsk branch of Far Eastern Scientific Centre of Physiology and Pathology of Respiration — Research Institute of Maternity and Childhood Protection. Additionally, MPM and lymphocyte populations were determined by flow cytometry. The degree of disturbed energy supply in the IBC was based on the data of simultaneous determination of lymphocyte, granulocyte and monocyte numbers with reduced MPM values (application for invention No. 2020115963), thus revealing 3 degrees of energy deficiency: 1 st degree, monovariant IBC composition with reduced MPM; 2 nd degree, bivariant composition, 3 rd degree, total changes. A relative and absolute decrease in CD3 (72% vs 78% and 1624 vs 1980), CD8 (28% vs 33% and 651 vs 851), an increase in CD19 (14% vs 9% and 304 vs 219) were revealed in pregnant women with PPROM. When assessing MPM values in the IBC populations, a decreased proportion of women without energy deficiency from the 1 st to the 2 nd trimester (from 41% to 30%), due to the 3 rd degree of energy deficiency (from 17% to 26%) was detected. A shift of affected pools at the 2 nd degree of energy deficiency in favor of lymphocytic-granulocytic association (from 7% to 25%) from lymphocytic-monocytic compartment (from 73% to 50%) was found. From the 2nd to 3rd trimester, we have detected redistribution of granulocyte pools at the 1 st degree (0 to 8%) and from the lymphocytic-granulocytic association (25% and 5%) to monocytic-granulocytic (25% and 40%). In the group with PPROM, there was a decreased proportion of pregnant women without energy deficiency (13% and 27%), as well as with the 1 st and 2 nd degrees (17% vs 31% and 9% vs 17%), due to the 3 rd degree of energy deficiency (61% and 26 %), relative to the comparison group. The IBC pools of in the main group were redistributed at the 1 st degree in favor of granulocytes (25% and 8%), at the 2 nd , in favor of the lymphocytic-monocytic association (100% and 55%) from the granulocytic-monocytic (0% and 40%). Such imbalance of bioenergetic processes in the IBC can be an important factor of pathologically ongoing inflammation. These changes could be caused by both higher incidence of infections in such patients and by alloimmune interactions between mother and fetus. However, they may also determine the pathological course of inflammation. Preterm birth, which is usually caused by PPROM, is a multifactorial pathological condition. However, independent on specific triggers, the changes in energy supply of IBC, at least, may serve as a significant biomarker of probability for this disorder.
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