Department of Paediatrics, Monash University, Melbourne, VIC 3168, Australia.
The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, VIC 3168, Australia.
Int J Mol Sci. 2023 Feb 22;24(5):4351. doi: 10.3390/ijms24054351.
Perinatal brain injury is a major contributor to long-term adverse neurodevelopment. There is mounting preclinical evidence for use of umbilical cord blood (UCB)-derived cell therapy as potential treatment. To systematically review and analyse effects of UCB-derived cell therapy on brain outcomes in preclinical models of perinatal brain injury. MEDLINE and Embase databases were searched for relevant studies. Brain injury outcomes were extracted for meta-analysis to calculate standard mean difference (SMD) with 95% confidence interval (CI), using an inverse variance, random effects model. Outcomes were separated based on grey matter (GM) and white matter (WM) regions where applicable. Risk of bias was assessed using SYRCLE, and GRADE was used to summarise certainty of evidence. Fifty-five eligible studies were included (7 large, 48 small animal models). UCB-derived cell therapy significantly improved outcomes across multiple domains, including decreased infarct size (SMD 0.53; 95% CI (0.32, 0.74), < 0.00001), apoptosis (WM, SMD 1.59; 95%CI (0.86, 2.32), < 0.0001), astrogliosis (GM, SMD 0.56; 95% CI (0.12, 1.01), = 0.01), microglial activation (WM, SMD 1.03; 95% CI (0.40, 1.66), = 0.001), neuroinflammation (TNF-α, SMD 0.84; 95%CI (0.44, 1.25), < 0.0001); as well as improved neuron number (SMD 0.86; 95% CI (0.39, 1.33), = 0.0003), oligodendrocyte number (GM, SMD 3.35; 95 %CI (1.00, 5.69), = 0.005) and motor function (cylinder test, SMD 0.49; 95 %CI (0.23, 0.76), = 0.0003). Risk of bias was determined as serious, and overall certainty of evidence was low. UCB-derived cell therapy is an efficacious treatment in pre-clinical models of perinatal brain injury, however findings are limited by low certainty of evidence.
围产期脑损伤是导致长期不良神经发育的主要原因。越来越多的临床前证据表明,脐带血(UCB)衍生的细胞疗法可作为潜在的治疗方法。本研究旨在系统地回顾和分析围产期脑损伤的临床前模型中 UCB 衍生细胞疗法对脑损伤结局的影响。检索了 MEDLINE 和 Embase 数据库中相关的研究。提取脑损伤结局进行荟萃分析,以计算标准均数差(SMD)和 95%置信区间(CI),采用逆方差、随机效应模型。根据灰物质(GM)和白物质(WM)区域进行了结果分离,如果适用的话。使用 SYRCLE 评估偏倚风险,并使用 GRADE 总结证据的确定性。纳入了 55 项符合条件的研究(7 项大型、48 项小动物模型)。UCB 衍生的细胞疗法在多个领域显著改善了结局,包括梗死面积减小(SMD 0.53;95%CI(0.32,0.74),<0.00001)、细胞凋亡减少(WM,SMD 1.59;95%CI(0.86,2.32),<0.0001)、星形胶质细胞增生减少(GM,SMD 0.56;95%CI(0.12,1.01),=0.01)、小胶质细胞激活减少(WM,SMD 1.03;95%CI(0.40,1.66),=0.001)、神经炎症减轻(TNF-α,SMD 0.84;95%CI(0.44,1.25),<0.0001);神经元数量增加(SMD 0.86;95%CI(0.39,1.33),=0.0003)、少突胶质细胞数量增加(GM,SMD 3.35;95%CI(1.00,5.69),=0.005)和运动功能改善(圆筒试验,SMD 0.49;95%CI(0.23,0.76),=0.0003)。偏倚风险被确定为严重,证据的总体确定性为低。UCB 衍生的细胞疗法在围产期脑损伤的临床前模型中是一种有效的治疗方法,然而,由于证据确定性低,结果受到限制。