Wang Yu, Song Huijie, Du Fanfan, Yang Zhongwen, Wang Yanli
Department of Pediatrics, Henan Provincial People's Hospital, Zhengzhou 450003, Henan, China. Corresponding author: Wang Yu, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2023 Dec;35(12):1268-1273. doi: 10.3760/cma.j.cn121430-20230313-00172.
To observe the effects of probiotics supplementation on the natural killer T cell (NKT cell) and inflammatory factors in children with sepsis and its protective effect on long-term lung function.
A total of 100 children with sepsis admitted to the department of pediatric intensive care unit (PICU) of Henan Provincial People's Hospital from March 2021 to May 2022 were selected as the research objects. The children were randomly divided into placebo group and probiotic group, 50 cases in each group. In addition to the conventional treatment, the probiotic group was given oral or nasal administration of 0.5 g probiotics, three times a day for 30 days, and the placebo group received oral placebo. 40 healthy children were selected as the healthy control group. The levels of interleukins (IL-4, IL-10), interferon-γ (IFN-γ) and immunoglobulin E (IgE), percentages of NKT cell in blood and induced sputum, lung function of the two groups of children with sepsis were measured before treatment, 7 days after treatment, and during follow-up. All these data were compared with those of healthy children. Kaplan-Meier analysis was used to compare the incidence of cough varied cough (CVA) between the two septic groups. Multiple linear regression analysis was used to explore the influence of various factors on the proportion of NKT cells in induced sputum.
In the placebo group, 2 cases died and 4 cases were lost to follow-up. In the probiotics group, 3 cases died and 5 cases were lost to follow-up. All the inflammatory factors of two groups decreased slowly after 7 day after treatment. There was no significance in the parameters of the two groups, but the levels of probiotic group declined more evidently. During the follow-up, a further decrease of inflammatory factors in probiotic group could be found, the levels of IL-4 and IL-10 were significantly different from those in the placebo group [IL-4 (ng/L): 20.3±9.3 vs. 27.6±11.9, IL-10 (ng/L): 23.1±6.8 vs. 14.4±4.4, both P < 0.05], with a significant decrease in IgE level (μg/L: 53.0±15.6 vs. 64.2±16.9, P < 0.05]. The results of flow cytometry showed that the percentage of NKT cell in peripheral blood in two septic groups decreased gradually, and the proportion of peripheral blood NKT cells in the probiotics group was significantly lower than that in the placebo group after 7 days of treatment [(4.2±0.9)% vs. (5.3±1.2)%, P < 0.05]. In the follow-up, the level of NKT cell in peripheral blood and induced sputum in probiotic group were lower than the placebo group [peripheral blood: (0.024±0.009)% vs. (0.029±0.008)%, induced sputum: (0.025±0.008)% vs. (0.035±0.01)%, both P < 0.05], which were similar to those in the healthy control group. Meanwhile, the percentage of predicted peak expiratory (PEF%) and ratio of forced expiratory volume in one second/forced vital capacity (FEV1/FVC) of probiotic group were higher than those in the placebo group [PEF%: (91.3±4.8)% vs. (85.8±8.6)%, FEV1/FVC ratio: (91.8±4.7)% vs. (87.2±7.4)%, both P < 0.05]. Although there was no significance in the incidence of CVA between two septic groups according to the Kaplan-Meier curve analysis, multiple linear regression analysis showed mechanical ventilation and allergic history were the risk factors for the increase of NKT cells [β values were 0.584, 0.601, 95% confidence interval (95%CI) were 0.069 to 1.099, 0.011 to 1.192, P = 0.027, 0.046], and probiotics was an independent protective factor for the relieve of increase in NKT cells (β value was -0.984,95%CI was -1.378 to -0.591, P = 0.001).
Application of probiotics to septic children early could promote the recovery of NKT cell and inflammatory factors, and alleviate the lung function injury induced by them during follow-up, which is helpful to improve the long-term prognosis of the patients.
观察补充益生菌对脓毒症患儿自然杀伤T细胞(NKT细胞)及炎症因子的影响及其对长期肺功能的保护作用。
选取2021年3月至2022年5月在河南省人民医院儿科重症监护病房(PICU)收治的100例脓毒症患儿作为研究对象。将患儿随机分为安慰剂组和益生菌组,每组50例。除常规治疗外,益生菌组给予口服或鼻饲0.5 g益生菌,每日3次,共30天,安慰剂组给予口服安慰剂。选取40例健康儿童作为健康对照组。分别在治疗前、治疗7天后及随访期间测量两组脓毒症患儿的白细胞介素(IL-4、IL-10)、干扰素-γ(IFN-γ)和免疫球蛋白E(IgE)水平、血液及诱导痰中NKT细胞百分比、肺功能。将所有这些数据与健康儿童的数据进行比较。采用Kaplan-Meier分析比较两组脓毒症患儿咳嗽变异性哮喘(CVA)的发生率。采用多元线性回归分析探讨各种因素对诱导痰中NKT细胞比例的影响。
安慰剂组死亡2例,失访4例。益生菌组死亡3例,失访5例。两组治疗7天后所有炎症因子均缓慢下降。两组参数无显著性差异,但益生菌组下降更明显。随访期间,益生菌组炎症因子进一步下降,IL-4和IL-10水平与安慰剂组有显著差异[IL-4(ng/L):20.3±9.3 vs. 27.6±11.9,IL-10(ng/L):23.1±6.8 vs. 14.4±4.4,均P<0.05],IgE水平显著降低(μg/L:53.0±15.6 vs. 64.2±16.9,P<0.05)。流式细胞术结果显示,两组脓毒症患儿外周血中NKT细胞百分比逐渐降低,治疗7天后益生菌组外周血NKT细胞比例显著低于安慰剂组[(4.2±0.9)% vs.(5.3±1.2)%,P<0.05]。随访期间,益生菌组外周血和诱导痰中NKT细胞水平低于安慰剂组[外周血:(0.024±0.009)% vs.(0.029±0.008)%,诱导痰:(0.025±0.008)% vs.(0.035±0.01)%,均P<0.05],与健康对照组相似。同时,益生菌组的预计呼气峰值百分比(PEF%)和一秒用力呼气容积/用力肺活量比值(FEV1/FVC)高于安慰剂组[PEF%:(91.3±4.8)% vs.(85.8±8.6)%,FEV1/FVC比值:(91.8±4.7)% vs.(87.2±7.4)%,均P<0.05]。虽然根据Kaplan-Meier曲线分析两组脓毒症患儿CVA的发生率无显著性差异,但多元线性回归分析显示机械通气和过敏史是NKT细胞增加的危险因素[β值分别为0.584、0.601,95%置信区间(95%CI)分别为0.069至1.099、0.011至1.192,P=0.027、0.046],而益生菌是缓解NKT细胞增加的独立保护因素(β值为-0.984,95%CI为-1.378至-0.591,P=0.001)。
早期对脓毒症患儿应用益生菌可促进NKT细胞和炎症因子的恢复,并减轻随访期间其所致的肺功能损伤,有助于改善患者的长期预后。