Glaser Kirsten, Speer Christian P
University Children's Hospital, University of Würzburg, Josef-Schneider-Str. 2, D-97080 Würzburg, Germany.
Expert Rev Anti Infect Ther. 2015 Feb;13(2):233-48. doi: 10.1586/14787210.2015.999670.
Colonization with Ureaplasma species has been associated with adverse pregnancy outcome, and perinatal transmission has been implicated in the development of bronchopulmonary dysplasia in preterm neonates. Little is known about Ureaplasma-mediated infection and inflammation of the CNS in neonates. Controversy remains concerning its incidence and implication in the pathogenesis of neonatal brain injury. In vivo and in vitro data are limited. Despite improving care options for extremely immature preterm infants, relevant complications remain. Systematic knowledge of ureaplasmal infection may be of great benefit. This review aims to summarize pathogenic mechanisms, clinical data and diagnostic pitfalls. Studies in preterm and term neonates are critically discussed with regard to their limitations. Clinical questions concerning therapy or prophylaxis are posed. We conclude that ureaplasmas may be true pathogens, especially in preterm neonates, and may cause CNS inflammation in a complex interplay of host susceptibility, serovar pathogenicity and gestational age-dependent CNS vulnerability.
解脲脲原体定植与不良妊娠结局相关,围产期传播被认为与早产儿支气管肺发育不良的发生有关。关于解脲脲原体介导的新生儿中枢神经系统感染和炎症知之甚少。其在新生儿脑损伤发病机制中的发生率和影响仍存在争议。体内和体外数据有限。尽管针对极不成熟的早产儿的护理选择有所改善,但相关并发症仍然存在。对解脲脲原体感染的系统认识可能大有裨益。本综述旨在总结致病机制、临床数据和诊断陷阱。对早产儿和足月儿的研究及其局限性进行了批判性讨论。提出了有关治疗或预防的临床问题。我们得出结论,解脲脲原体可能是真正的病原体,尤其是在早产儿中,并且可能在宿主易感性、血清型致病性和孕周依赖性中枢神经系统易损性的复杂相互作用中导致中枢神经系统炎症。