Dean Justin M, Shi Zhongjie, Fleiss Bobbi, Gunn Katherine C, Groenendaal Floris, van Bel Frank, Derrick Matthew, Juul Sandra E, Tan Sidhartha, Gressens Pierre, Mallard Carina, Bennet Laura, Gunn Alistair J
Department of Physiology, University of Auckland, Auckland, New Zealand.
Dev Neurosci. 2015;37(4-5):289-304. doi: 10.1159/000370309. Epub 2015 Feb 19.
One of the central, unanswered questions in perinatology is why preterm infants continue to have such poor long-term neurodevelopmental, cognitive and learning outcomes, even though severe brain injury is now rare. There is now strong clinical evidence that one factor underlying disability may be infection, as well as nonspecific inflammation, during fetal and early postnatal life. In this review, we examine the experimental evidence linking both acute and chronic infection/inflammation with perinatal brain injury and consider key experimental determinants, including the microglia response, relative brain and immune maturity and the pattern of exposure to infection. We highlight the importance of the origin and derivation of the bacterial cell wall component lipopolysaccharide. Such experimental paradigms are essential to determine the precise time course of the inflammatory reaction and to design targeted neuroprotective strategies to protect the perinatal brain from infection and inflammation.
围产医学中一个核心且尚未解决的问题是,尽管严重脑损伤如今已很罕见,但早产儿为何仍持续存在如此糟糕的长期神经发育、认知和学习结果。现在有强有力的临床证据表明,导致残疾的一个因素可能是胎儿期和出生后早期的感染以及非特异性炎症。在这篇综述中,我们审视了将急性和慢性感染/炎症与围产期脑损伤联系起来的实验证据,并考虑了关键的实验决定因素,包括小胶质细胞反应、相对脑成熟度和免疫成熟度以及感染暴露模式。我们强调了细菌细胞壁成分脂多糖的来源和衍生的重要性。此类实验范式对于确定炎症反应的确切时间进程以及设计有针对性的神经保护策略以保护围产期脑免受感染和炎症至关重要。