Yazdi Siamak M, Patel Ekta U, Richardson Colby D, Hardy K Thomas, Baatz John E, Mulligan Jennifer K, Ryan Rita M
Department of Pediatrics-Neonatology, Medical University of South Carolina, Charleston, SC 29425, USA.
Department of Pediatrics-Neonatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Children (Basel). 2021 Oct 2;8(10):879. doi: 10.3390/children8100879.
Postnatal corticosteroids improve respiratory status and facilitate respiratory support weaning in preterm infants with bronchopulmonary dysplasia (BPD). Older literature describes characteristic cytokine profiles in tracheal aspirates (TA) of BPD patients which are altered with corticosteroids. Corticosteroids also influence peripheral blood T-cell presence. However, little is known regarding TA T-cell phenotype and cytokine production before or after exogenous corticosteroids. We hypothesized that postnatal dexamethasone alters the TA T-cell cytokine profiles of preterm infants. TA samples were collected from 14 infants born from 23 0/7 to 28 6/7 weeks who were mechanically ventilated for at least 14 days. Samples were collected up to 72 h before a ten-day dexamethasone course and again 1 to 3 calendar days after dexamethasone initiation. The primary outcome was change in T cell populations present in TA and their intracellular cytokine profile after dexamethasone treatment, ascertained via flow cytometry. Following dexamethasone treatment, there were significant decreases in respiratory severity score (RSS), percent CD4+IL-6+ cells, CD8+IL-6+ cells, CXCR3+IL-6+ cells, and CXCR3+IL-2+ cells and total intracellular IFN-γ in TA. RSS significantly correlated with TA percent CD4+IL-6+ cells. To our knowledge, this is the first study demonstrating that dexamethasone reduced T-cell IL-6 and this reduction was associated with improved RSS in pre-term infants with evolving BPD.
产后使用皮质类固醇可改善支气管肺发育不良(BPD)早产儿的呼吸状况并促进呼吸支持的撤离。早期文献描述了BPD患者气管吸出物(TA)中的特征性细胞因子谱,这些谱会因皮质类固醇而改变。皮质类固醇还会影响外周血T细胞的存在。然而,关于外源性皮质类固醇使用前后TA中T细胞表型和细胞因子产生的情况知之甚少。我们假设产后地塞米松会改变早产儿TA中的T细胞细胞因子谱。从14名孕周为23 0/7至28 6/7周、机械通气至少14天的婴儿中采集TA样本。在为期十天的地塞米松疗程开始前72小时内采集样本,并在地塞米松开始使用后的1至3个日历日内再次采集。主要结局是地塞米松治疗后TA中存在的T细胞群体及其细胞内细胞因子谱的变化,通过流式细胞术确定。地塞米松治疗后,TA中的呼吸严重程度评分(RSS)、CD4 + IL-6 +细胞百分比、CD8 + IL-6 +细胞百分比、CXCR3 + IL-6 +细胞百分比、CXCR3 + IL-2 +细胞百分比以及细胞内总IFN-γ均显著下降。RSS与TA中CD4 + IL-6 +细胞百分比显著相关。据我们所知,这是第一项表明地塞米松可降低T细胞IL-6水平且这种降低与患有进展性BPD的早产儿RSS改善相关的研究。