Department of Internal Medicine, Division of Nephrology & Hypertension, Texas A & M Health Science Center/Scott & White Memorial Hospital, 702 SW HK Dodgen Loop, Temple, TX 76504, USA.
Placenta. 2011 Mar;32(3):201-5. doi: 10.1016/j.placenta.2010.12.026. Epub 2011 Feb 2.
Dysregulation of the maternal immune system during pregnancy has been implicated in the development of preeclampsia (PE), however the pathogenetic signals and mechanisms have not been completely elucidated. Here we provide a hypothesis and evidence that dsRNA is a danger signal leading to maternal immune system activation and an "antiviral" immune response that manifests as PE. dsRNA released from necrotic cells and/or from viruses causes excessive activation of dsRNA receptors and PE-like symptoms in animals. Additionally, high expression levels of dsRNA receptors have been identified in human and animal placental tissue as well as trophoblast cells, and these receptors appear to be excessively activated in PE. These key components of the innate immune system that respond to invading pathogens and dead or necrotic tissue likely play a major role in the development of PE.
母体免疫系统在怀孕期间的失调与子痫前期(PE)的发展有关,然而其致病信号和机制尚未完全阐明。在这里,我们提出了一个假设和证据,即 dsRNA 是一种危险信号,导致母体免疫系统激活和表现为 PE 的“抗病毒”免疫反应。来自坏死细胞和/或病毒的 dsRNA 释放会导致 dsRNA 受体过度激活,并在动物中引起类似 PE 的症状。此外,在人和动物的胎盘组织以及滋养层细胞中已经鉴定出 dsRNA 受体的高表达水平,并且这些受体在 PE 中似乎过度激活。这些先天免疫系统的关键组成部分,可响应入侵病原体和死亡或坏死组织,可能在 PE 的发展中发挥主要作用。