Center for International Health Research, Rhode Island Hospital, Brown University Medical School, Providence, Rhode Island, United States of America.
PLoS Negl Trop Dis. 2013 Jun 6;7(6):e2253. doi: 10.1371/journal.pntd.0002253. Print 2013.
Schistosomiasis affects nearly 40 million women of reproductive age, and is known to elicit a pro-inflammatory signature in the placenta. We have previously shown that antigens from schistosome eggs can elicit pro-inflammatory cytokine production from trophoblast cells specifically; however, the influence of these antigens on other characteristics of trophoblast function, particularly as it pertains to placentation in early gestation, is unknown. We therefore sought to determine the impact of schistosome antigens on key characteristics of first trimester trophoblast cells, including migration and invasion.
First trimester HTR8/SVneo trophoblast cells were co-cultured with plasma from pregnant women with and without schistosomiasis or schistosome soluble egg antigens (SEA) and measured cytokine, cellular migration, and invasion responses.
Exposure of HTR8 cells to SEA resulted in a pro-inflammatory, anti-invasive signature, characterized by increased pro-inflammatory cytokines (IL-6, IL-8, MCP-1) and TIMP-1. Additionally, these cells displayed 62% decreased migration and 2.7-fold decreased invasion in vitro after treatment with SEA. These results are supported by increased IL-6 and IL-8 in the culture media of HTR8 cells exposed to plasma from Schistosoma japonica infected pregnant women.
Soluble egg antigens found in circulation during schistosome infection increase pro-inflammatory cytokine production and inhibit the mobility and invasive characteristics of the first trimester HTR8/SVneo trophoblast cell line. This is the first study to assess the impact of schistosome soluble egg antigens on the behavior of an extravillous trophoblast model and suggests that schistosomiasis in the pre-pregnancy period may adversely impact placentation and the subsequent health of the mother and newborn.
血吸虫病影响近 4000 万育龄妇女,已知其在胎盘内引发促炎特征。我们之前已经表明,血吸虫卵的抗原可以特异性地引起滋养细胞产生促炎细胞因子;然而,这些抗原对滋养细胞功能的其他特征的影响,特别是在妊娠早期与胎盘形成有关的特征,尚不清楚。因此,我们试图确定血吸虫抗原对早孕滋养细胞的关键特征的影响,包括迁移和侵袭。
将早孕 HTR8/SVneo 滋养细胞与患有和不患有血吸虫病或血吸虫可溶性卵抗原(SEA)的孕妇的血浆共培养,并测量细胞因子、细胞迁移和侵袭反应。
SEA 暴露于 HTR8 细胞导致促炎、抗侵袭特征,其特征为促炎细胞因子(IL-6、IL-8、MCP-1)和 TIMP-1 增加。此外,在用 SEA 处理后,这些细胞的体外迁移减少了 62%,侵袭减少了 2.7 倍。这些结果得到了在 HTR8 细胞暴露于感染日本血吸虫的孕妇血浆的培养物中增加的 IL-6 和 IL-8 的支持。
在血吸虫感染期间循环中发现的可溶性卵抗原增加了促炎细胞因子的产生,并抑制了早孕 HTR8/SVneo 滋养细胞系的迁移和侵袭特征。这是第一项评估血吸虫可溶性卵抗原对绒毛外滋养细胞模型行为影响的研究,表明妊娠前血吸虫病可能对胎盘形成以及母亲和新生儿的后续健康产生不利影响。