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Maternal Adaptive Immune Cells in Decidua Parietalis Display a More Activated and Coinhibitory Phenotype Compared to Decidua Basalis

机译:与蜕膜蜕膜相比蜕膜蜕膜中的母体适应性免疫细胞表现出更多的活化和抑制性表型。

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摘要

The maternal part of the placenta, the decidua, consists of maternal immune cells, decidual stromal cells, and extravillous fetal trophoblasts. In a successful pregnancy, these cell compartments interact to provide an intricate balance between fetal tolerance and antimicrobial defense. These processes are still poorly characterized in the two anatomically different decidual tissues, basalis and parietalis. We examined immune cells from decidua basalis and parietalis from term placentas (n = 15) with flow cytometry. By using multivariate discriminant analysis, we found a clear separation between the two decidual compartments based on the 81 investigated parameters. Decidua parietalis lymphocytes displayed a more activated phenotype with a higher expression of coinhibitory markers than those isolated from basalis and contained higher frequencies of T regulatory cells. Decidua basalis contained higher proportions of monocytes, B cells, and mucosal-associated invariant T (MAIT) cells. The basalis B cells were more immature, and parietalis MAIT cells showed a more activated phenotype. Conventional T cells, NK cells, and MAIT cells from both compartments potently responded with the production of interferon-γ and/or cytotoxic molecules in response to stimulation. To conclude, leukocytes in decidua basalis and parietalis displayed remarkable phenotypic disparities, indicating that the corresponding stromal microenvironments provide different immunoregulatory signals.
机译:胎盘的母体蜕膜由母体免疫细胞,蜕膜性基质细胞和绒毛外滋养层组成。在一次成功的妊娠中,这些细胞区室相互作用以在胎儿耐受性和抗菌防御之间提供复杂的平衡。这些过程在两个解剖学上不同的蜕膜组织,基底肌和顶叶肌中仍然缺乏良好的特征。我们用流式细胞术检查了来自足底蜕膜的蜕膜和足月胎盘(n = 15)的壁突。通过使用多元判别分析,我们根据81个调查参数发现了两个蜕膜区室之间的明确分离。与从基底膜分离的那些相比,顶叶蜕膜的淋巴细胞表现出更高的活化表型和更高的共抑制标记物表达,并且含有更高频率的T调节细胞。蜕膜蜕膜含有较高比例的单核细胞,B细胞和与粘膜相关的不变T(MAIT)细胞。基底B细胞更不成熟,顶壁MAIT细胞表现出更多的活化表型。来自两个隔室的常规T细胞,NK细胞和MAIT细胞响应刺激而有效地产生干扰素-γ和/或细胞毒性分子。总的来说,蜕膜和蜕膜中的白细胞表现出明显的表型差异,表明相应的基质微环境提供了不同的免疫调节信号。

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