Transplantation Unit, Renal Division, Department of Medicine, University Health Center of Quebec, Faculty of Medicine, Laval University, Quebec City, QC, Canada.
Hematology and Oncology Division, Department of Medicine, University Health Center of Quebec, Faculty of Medicine, Laval University, Quebec City, QC, Canada.
J Thromb Haemost. 2017 May;15(5):1020-1031. doi: 10.1111/jth.13661. Epub 2017 Mar 21.
Essentials The effect of alloantibodies on the endothelial expression of thrombomodulin is unknown. Thrombomodulin was quantified in stimulated endothelial cells and measured in serum samples. Anti-human leukocyte antigen (HLA) I vs. II antibodies have different effects on thrombomodulin. Anti-HLA II antibodies may promote a prothrombotic state and contribute to microangiopathy.
Rationale Thrombomodulin (TBM) is an anticoagulant and anti-inflammatory transmembrane protein expressed on endothelial cells. Donor-specific alloantibodies, particularly those against human leukocyte antigen (HLA) class II, are associated with microvascular endothelial damage in solid allografts. Objective Our aim was to characterize the effects of anti-HLA antibodies on endothelial expression of TBM, and in particular, the differential effects of anti-HLA class I compared with those of anti-HLA class II. Methods We used human glomerular microvascular endothelial cells to examine TBM expression on anti-HLA-treated cells, and we tested sera from transplant recipients for soluble TBM. Results We found that whereas membrane TBM expression increased in a dose-dependent manner in the presence of anti-HLA class I antibodies, treatment with anti-HLA class II led to minimal TBM expression on the endothelial surface but to a cytosolic accumulation. Platelet adhesion studies confirmed the functional impact of anti-HLA class II. Quantitative densitometry of the membrane lysates further suggested that anti-HLA class II impairs TBM glycosylation. Furthermore, we found a significant association between the presence of circulating anti-HLA class II antibodies in transplant recipients and low serum levels of TBM. Conclusion These results indicate that ligation of anti-HLA class I and II antibodies produces different effects on the endothelial expression of TBM and on serum levels of TBM in transplant recipients. Anti-HLA class II antibodies may be associated with a prothrombotic state, which could explain the higher occurrence of microangiopathic lesions in the allograft and the poor outcomes observed in patients with these alloantibodies.
目的 血栓调节蛋白(TBM)是一种抗凝和抗炎的跨膜蛋白,在血管内皮细胞中表达。供体特异性同种抗体,特别是针对人类白细胞抗原(HLA)II 类的抗体,与实体同种异体移植物中的微血管内皮损伤有关。
方法 我们使用人肾小球微血管内皮细胞来研究抗 HLA 处理细胞上 TBM 的表达,并用移植受者的血清检测可溶性 TBM。
结果 我们发现,抗 HLA I 类抗体存在时,TBM 膜表达呈剂量依赖性增加,而抗 HLA II 类抗体则导致内皮表面 TBM 表达最小,但细胞质内积累。血小板黏附研究证实了抗 HLA II 类的功能影响。膜裂解物的定量密度测定进一步表明,抗 HLA II 类抗体损害了 TBM 的糖基化。此外,我们发现移植受者中循环抗 HLA II 类抗体的存在与 TBM 血清水平降低之间存在显著关联。
结论 这些结果表明,抗 HLA I 类和 II 类抗体对内皮细胞 TBM 的表达以及移植受者 TBM 的血清水平产生不同的影响。抗 HLA II 类抗体可能与血栓形成状态有关,这可以解释同种异体移植物中微血管病变发生率较高,以及这些同种抗体患者预后较差的原因。