van den Bosch Thierry P P, Caliskan Kadir, Kraaij Marina D, Constantinescu Alina A, Manintveld Olivier C, Leenen Pieter J M, von der Thüsen Jan H, Clahsen-van Groningen Marian C, Baan Carla C, Rowshani Ajda T
Department of Internal Medicine and Transplantation, Erasmus University Medical Center , Rotterdam , Netherlands.
Department of Cardiology, Erasmus University Medical Center , Rotterdam , Netherlands.
Front Immunol. 2017 Mar 24;8:346. doi: 10.3389/fimmu.2017.00346. eCollection 2017.
During acute heart transplant rejection, infiltration of lymphocytes and monocytes is followed by endothelial injury and eventually myocardial fibrosis. To date, no information is available on monocyte-macrophage-related cellular shifts and their polarization status during rejection. Here, we aimed to define and correlate monocyte-macrophage endomyocardial tissue profiles obtained at rejection and time points prior to rejection, with corresponding serial blood samples in 25 heart transplant recipients experiencing acute cellular rejection. Additionally, 33 healthy individuals served as control.
Using histology, immunohistochemistry, confocal laser scan microscopy, and digital imaging expression of CD14, CD16, CD56, CD68, CD80, and CD163 were explored to define monocyte and macrophage tissue profiles during rejection. Fibrosis was investigated using Sirius Red stainings of rejection, non-rejection, and 1-year biopsies. Expression of co-stimulatory and migration-related molecules on circulating monocytes, and production potential for pro- and anti-inflammatory cytokines were studied using flow cytometry.
At tissue level, striking CD16+ monocyte infiltration was observed during rejection ( < 0.001). Significantly more CD68+CD163+ M2 macrophages were documented during rejection compared to barely present CD68+CD80+ M1 macrophages. Rejection was associated with severe fibrosis in 1-year biopsies ( < 0.001). Irrespective of rejection status, decreased frequencies of circulating CD16+ monocytes were found in patients compared to healthy individuals. Rejection was reflected by significantly increased CD54 and HLA-DR expression on CD16+ monocytes with retained cytokine production potential.
CD16+ monocytes and M2 macrophages hallmark the correlates of heart transplant acute cellular rejection on tissue level and seem to be associated with fibrosis in the long term.
在急性心脏移植排斥反应期间,淋巴细胞和单核细胞浸润后会出现内皮损伤,最终导致心肌纤维化。迄今为止,尚无关于排斥反应期间单核细胞 - 巨噬细胞相关细胞变化及其极化状态的信息。在此,我们旨在确定25名经历急性细胞排斥反应的心脏移植受者在排斥反应时以及排斥反应前各时间点获得的单核细胞 - 巨噬细胞心内膜心肌组织特征,并将其与相应的系列血样进行关联分析。另外,33名健康个体作为对照。
使用组织学、免疫组织化学、共聚焦激光扫描显微镜以及数字成像技术,探究CD14、CD16、CD56、CD68、CD80和CD163的表达,以确定排斥反应期间的单核细胞和巨噬细胞组织特征。使用天狼星红染色法对排斥反应、非排斥反应以及1年活检组织进行纤维化研究。使用流式细胞术研究循环单核细胞上共刺激分子和迁移相关分子的表达,以及促炎和抗炎细胞因子的产生潜力。
在组织水平上,排斥反应期间观察到显著的CD16 + 单核细胞浸润(<0.001)。与几乎不存在的CD68 + CD80 + M1巨噬细胞相比,排斥反应期间记录到显著更多的CD68 + CD163 + M2巨噬细胞。排斥反应与1年活检组织中的严重纤维化相关(<0.001)。与健康个体相比,无论排斥状态如何,患者循环CD16 + 单核细胞的频率均降低。排斥反应表现为CD16 + 单核细胞上CD54和HLA - DR表达显著增加,且细胞因子产生潜力得以保留。
CD16 + 单核细胞和M2巨噬细胞是心脏移植急性细胞排斥反应在组织水平上的特征标志,并且从长期来看似乎与纤维化相关。