Department of Obstetrics & Gynecology, University of Washington, Seattle, Washington, USA.
PLoS One. 2011;6(12):e28972. doi: 10.1371/journal.pone.0028972. Epub 2011 Dec 21.
Early events leading to intrauterine infection and fetal lung injury remain poorly defined, but may hold the key to preventing neonatal and adult chronic lung disease. Our objective was to establish a nonhuman primate model of an early stage of chorioamnionitis in order to determine the time course and mechanisms of fetal lung injury in utero.
METHODOLOGY/PRINCIPAL FINDINGS: Ten chronically catheterized pregnant monkeys (Macaca nemestrina) at 118-125 days gestation (term=172 days) received one of two treatments: 1) choriodecidual and intra-amniotic saline (n=5), or 2) choriodecidual inoculation of Group B Streptococcus (GBS) 1×10(6) colony forming units (n=5). Cesarean section was performed regardless of labor 4 days after GBS or 7 days after saline infusion to collect fetal and placental tissues. Only two GBS animals developed early labor with no cervical change in the remaining animals. Despite uterine quiescence in most cases, blinded review found histopathological evidence of fetal lung injury in four GBS animals characterized by intra-alveolar neutrophils and interstitial thickening, which was absent in controls. Significant elevations of cytokines in amniotic fluid (TNF-α, IL-8, IL-1β, IL-6) and fetal plasma (IL-8) were detected in GBS animals and correlated with lung injury (p<0.05). Lung injury was not directly caused by GBS, because GBS was undetectable in amniotic fluid (~10 samples tested/animal), maternal and fetal blood by culture and polymerase chain reaction. In only two cases was GBS cultured from the inoculation site in low numbers. Chorioamnionitis occurred in two GBS animals with lung injury, but two others with lung injury had normal placental histology.
CONCLUSIONS/SIGNIFICANCE: A transient choriodecidual infection can induce cytokine production, which is associated with fetal lung injury without overt infection of amniotic fluid, chorioamnionitis or preterm labor. Fetal lung injury may, thus, occur silently without symptoms and before the onset of the fetal systemic inflammatory response syndrome.
导致宫内感染和胎儿肺损伤的早期事件仍未得到明确界定,但可能是预防新生儿和成人慢性肺部疾病的关键。我们的目的是建立一个人类胎猴的绒毛膜羊膜炎早期模型,以确定胎儿肺损伤在宫内的发生过程和机制。
方法/主要发现:10 只接受长期导管植入的怀孕猕猴(Macaca nemestrina)在 118-125 天妊娠(足月=172 天)时接受以下两种治疗之一:1)绒毛膜羊膜腔和羊膜内生理盐水(n=5),或 2)绒毛膜羊膜炎接种 B 群链球菌(GBS)1×10(6)菌落形成单位(n=5)。无论 GBS 或生理盐水输注后 4 天或 7 天后是否发生早产,均行剖宫产术以收集胎儿和胎盘组织。只有 2 只 GBS 动物出现早期分娩,但其余动物的宫颈无变化。尽管大多数情况下子宫静止,但盲法检查发现 4 只 GBS 动物的胎儿肺损伤具有肺泡内中性粒细胞和间质增厚的组织病理学证据,而对照组无此特征。GBS 动物的羊水(TNF-α、IL-8、IL-1β、IL-6)和胎儿血浆(IL-8)中的细胞因子显著升高,并与肺损伤相关(p<0.05)。肺损伤不是由 GBS 直接引起的,因为在羊水(~10 个动物样本/动物)、母血和胎儿血中通过培养和聚合酶链反应均未检测到 GBS。仅在 2 例中从接种部位培养出低数量的 GBS。2 只发生肺损伤的 GBS 动物发生绒毛膜羊膜炎,但另外 2 只发生肺损伤的动物胎盘组织学正常。
结论/意义:短暂的绒毛膜羊膜炎感染可引起细胞因子的产生,与羊水、绒毛膜羊膜炎或早产无关,但与胎儿肺损伤相关。因此,胎儿肺损伤可能在没有症状且胎儿全身炎症反应综合征发生之前就已悄悄发生。