White matter injury following fetal inflammatory response syndrome induced by chorioamnionitis and fetal sepsis: Lessons from experimental ovine models

• Published in: Early human development 2012-12, Vol.88 (12), p.931-936
• Main Authors: Kuypers, Elke, Ophelders, Daan, Jellema, Reint K, Kunzmann, Steffen, Gavilanes, Antonio W, Kramer, Boris W
• Format: Article
• Language: English
• Subjects: Advanced Basic Science; Animals; Biological and medical sciences; Brain Diseases - etiology; Brain Diseases - physiopathology; Cerebral palsy; Chorioamnionitis - physiopathology; Disease Models, Animal; Embryology: invertebrates and vertebrates. Teratology; Female; Fundamental and applied biological sciences. Psychology; Humans; Intra-uterine inflammation; Microglia; Neonatal and Perinatal Medicine; Oligodendrocytes; Pregnancy; Pregnancy Complications, Infectious; Sheep, Domestic; Systemic Inflammatory Response Syndrome - complications
• ISSN: 0378-3782; 1872-6232
• DOI: 10.1016/j.earlhumdev.2012.09.011

Abstract Chorioamnionitis and fetal sepsis can induce a fetal inflammatory response syndrome (FIRS) which is closely related to the development of white matter injury in the fetal brain. Large epidemiological studies support the link between FIRS and fetal brain injury with a clear association between the presence of in utero inflammation and neurodevelopmental complications such as cerebral palsy, autism and cognitive impairments later in life. Translational animal models of chorioamnionitis and fetal sepsis are essential in understanding the underlying pathophysiological mechanisms of fetal brain injury after exposure to intra-uterine inflammation. Concerning this aspect, ovine models have high translational value since neurodevelopment in sheep closely resembles the human situation. In this article, we will review clinical and experimental evidence for the link between FIRS and white matter injury in the fetal brain. With respect to experimental findings, we will particularly focus on the lessons learned from ovine models of chorioamnionitis and fetal sepsis. We also highlight two key players implied in the pathophysiology of white matter injury after in utero exposure to inflammation.