Pontoppidan Peter L, Jordan Karina, Carlsen Anting Liu, Uhlving Hilde Hylland, Kielsen Katrine, Christensen Mette, Ifversen Marianne, Nielsen Claus Henrik, Sangild Per, Heegaard Niels Henrik Helweg, Heilmann Carsten, Sengeløv Henrik, Müller Klaus
Rigshospitalet, Copenhagen, Denmark; Department of Nutrition, Exercise and Sports, University of Copenhagen, Denmark.
Rigshospitalet, Copenhagen, Denmark; Institute for Inflammation Research, Department of Infectious Diseases and Rheumatology, Rigshospitalet, Copenhagen, Denmark.
Int Immunopharmacol. 2015 Mar;25(1):180-8. doi: 10.1016/j.intimp.2014.12.038. Epub 2015 Jan 20.
Allogeneic hematopoietic stem cell transplantation (HSCT) is a procedure with a high risk of treatment related mortality. The primary aim of the present study was to examine associations between markers of gastrointestinal toxicity, markers of systemic inflammation, and plasma levels of microRNA (miRNA) -155 and -146a during the first month after HSCT. The secondary aim was to characterize the impact of the toxic-inflammatory response on the function of circulating leukocytes during immune recovery. Thirty HSCT patients were included. Gastrointestinal injury was monitored by toxicity scores, lactulose-mannitol test and plasma citrulline, as a measure of the enterocyte population. Nadir of citrulline and maximum of oral toxicity scores, intestinal permeability, CRP and plasma levels of IL-6 and IL-10 was seen at day +7 post-HSCT. miRNA-155 and mi-RNA-146a showed an inverse relation with significantly elevated miRNA-155 and decreased miRNA-146a levels, from day 0 to day +28 compared with pre-conditioning levels. Citrulline levels below the median at day +7 were associated with higher spontaneous production of IL-6 and TNF-α as well as higher in vitro stimulated production of IL-17A at day +21. This study is the first to demonstrate that toxic responses to chemotherapy are accompanied by differential regulation of miRNAs with opposing effects on immune regulation. We find that a proinflammatory miRNA profile is sustained during the first three weeks after the transplantation, indicating that these miRNAs may play a role in the regulation of the inflammatory environment during immune reconstitution after HSCT.
异基因造血干细胞移植(HSCT)是一种治疗相关死亡率很高的治疗手段。本研究的主要目的是检测HSCT后第一个月内胃肠道毒性标志物、全身炎症标志物与血浆微小RNA(miRNA)-155和-146a水平之间的关联。次要目的是描述毒性炎症反应对免疫恢复过程中循环白细胞功能的影响。纳入了30例HSCT患者。通过毒性评分、乳果糖-甘露醇试验和血浆瓜氨酸监测胃肠道损伤,血浆瓜氨酸可作为肠上皮细胞群的指标。瓜氨酸最低点以及口服毒性评分、肠道通透性、CRP以及IL-6和IL-10血浆水平的最高点出现在HSCT后第7天。与预处理水平相比,从第0天到第28天,miRNA-155和miRNA-146a呈负相关,miRNA-155水平显著升高,miRNA-146a水平降低。第7天瓜氨酸水平低于中位数与第21天IL-6和TNF-α的自发产生增加以及IL-17A的体外刺激产生增加有关。本研究首次证明化疗的毒性反应伴随着对免疫调节有相反作用的miRNA的差异调节。我们发现移植后的前三周促炎miRNA谱持续存在,这表明这些miRNA可能在HSCT后免疫重建过程中的炎症环境调节中发挥作用。