Department of Haematology and Oncology, University Cancer Centre Hamburg (UCCH), University Medical Centre Eppendorf, Hamburg, Germany.
Institute of Clinical Chemistry and Laboratory Medicine, University Medical Centre Eppendorf, Hamburg, Germany.
Ann Hematol. 2020 Jul;99(7):1531-1542. doi: 10.1007/s00277-020-04075-6. Epub 2020 May 19.
In haemophilia, thrombin generation and fibrin deposition upon vascular injury critically depend on the tissue factor (TF)-driven coagulation pathway. TF expression by monocytes/macrophages and circulating microvesicles contributes to haemostasis, thrombosis and inflammation. Inflammation is a hallmark of blood-induced joint disease. The aim of this study is to correlate TF production by whole-blood monocytes with inflammatory markers and clinical parameters in patients with moderate-to-severe haemophilia A or B (n = 43) in comparison to healthy males (n = 23). Monocyte TF antigen and microvesicle-associated TF procoagulant activity (MV TF PCA) were measured immediately after blood draw (baseline) and following incubation of whole blood with buffer or lipopolysaccharide (LPS) using two-colour flow cytometry and chromogenic FXa generation assay, respectively. Patients with HIV or uncontrolled HBV/HCV infections were excluded. TF was hardly detectable and not different in baseline and buffer-treaded samples from both groups. Stimulation with LPS, however, induced monocyte TF production, with increased TF-specific mean fluorescence intensity (P = 0.08) and MV TF PCA (P < 0.05) in patients compared to controls. Patients also had elevated hs-CRP and IL-6 serum levels (P < 0.001), which correlated with LPS-induced TF parameters. Further exploratory analyses revealed that the presence of systemic (low-grade) inflammation and boosted LPS-induced monocyte TF production were mainly restricted to patients with clinically controlled HBV and/or HCV infection (n = 16), who were older and also had a significantly worse orthopaedic joint score than patients with no history of viral hepatitis (P < 0.01). Our study delineates a previously unrecognised link between systemic inflammation and inducible monocyte TF production in patients with haemophilia A or B.
在血友病中,血管损伤时的凝血酶生成和纤维蛋白沉积严重依赖于组织因子(TF)驱动的凝血途径。单核细胞/巨噬细胞和循环微泡中的 TF 表达有助于止血、血栓形成和炎症。炎症是血液诱导关节疾病的标志。本研究旨在比较伴有中重度血友病 A 或 B(n=43)的患者与健康男性(n=23)的全血单核细胞 TF 产生与炎症标志物和临床参数的相关性。使用双色流式细胞术和显色 FXa 生成测定法,分别在采血后立即(基线)和全血与缓冲液或脂多糖(LPS)孵育后测量单核细胞 TF 抗原和微泡相关 TF 促凝活性(MV TF PCA)。排除 HIV 或未控制的 HBV/HCV 感染的患者。两组基线和缓冲处理样本中 TF 几乎无法检测到且无差异。然而,用 LPS 刺激诱导单核细胞 TF 产生,与对照组相比,患者的 TF 特异性平均荧光强度(P=0.08)和 MV TF PCA(P<0.05)增加。患者还具有升高的 hs-CRP 和 IL-6 血清水平(P<0.001),与 LPS 诱导的 TF 参数相关。进一步的探索性分析表明,全身性(低度)炎症的存在和 LPS 诱导的单核细胞 TF 产生的增加主要局限于具有临床控制 HBV 和/或 HCV 感染的患者(n=16),这些患者年龄较大,且与无病毒性肝炎史的患者相比,骨科关节评分明显更差(P<0.01)。本研究描绘了血友病 A 或 B 患者中系统性炎症与可诱导单核细胞 TF 产生之间以前未被识别的联系。