Hematology Department-BMT Unit, G Papanicolaou Hospital, 57010 Thessaloniki, Greece.
3rd Department of Internal Medicine, Papageorgiou Hospital, Aristotle University of Thessaloniki, 56403 Thessaloniki, Greece.
Int J Mol Sci. 2020 Dec 21;21(24):9768. doi: 10.3390/ijms21249768.
(1) Background: survivors of allogeneic hematopoietic cell transplantation (alloHCT) suffer from morbidity and mortality due to cardiovascular events. We hypothesized that vascular injury and pro-coagulant activity are evident in alloHCT survivors without existing alloHCT complications or relapse. (2) Methods: we enrolled consecutive adult alloHCT survivors without established cardiovascular disease and control individuals matched for traditional cardiovascular risk factors (January-December 2019). Circulating microvesicles (MVs) of different cellular origins (platelet, erythrocyte, and endothelial) were measured by a standardized flow cytometry protocol as novel markers of vascular injury and pro-coagulant activity. (3) Results: we recruited 45 survivors after a median of 2.3 (range 1.1-13.2) years from alloHCT, and 45 controls. The majority of patients suffered from acute (44%) and/or chronic (66%) graft-versus-host disease (GVHD). Although the two groups were matched for traditional cardiovascular risk factors, alloHCT survivors showed significantly increased platelet and erythrocyte MVs compared to controls. Within alloHCT survivors, erythrocyte MVs were significantly increased in patients with a previous history of thrombotic microangiopathy. Interestingly, endothelial MVs were significantly increased only in alloHCT recipients of a myeloablative conditioning. Furthermore, MVs of different origins showed a positive association with each other. (4) Conclusions: endothelial dysfunction and increased thrombotic risk are evident in alloHCT recipients long after alloHCT, independently of traditional cardiovascular risk factors. An apparent synergism of these pathophysiological processes may be strongly involved in the subsequent establishment of cardiovascular disease.
(1) 背景:异基因造血细胞移植(alloHCT)的幸存者因心血管事件而遭受发病率和死亡率。我们假设,在没有现有 alloHCT 并发症或复发的 alloHCT 幸存者中,血管损伤和促凝活性是明显的。(2) 方法:我们招募了连续的无既定心血管疾病的成年 alloHCT 幸存者和匹配传统心血管危险因素的对照个体(2019 年 1 月至 12 月)。通过标准化的流式细胞术方案测量不同细胞来源(血小板、红细胞和内皮细胞)的循环微泡(MVs),作为血管损伤和促凝活性的新型标志物。(3) 结果:我们招募了 45 名 alloHCT 后中位数为 2.3 年(范围 1.1-13.2 年)的幸存者和 45 名对照。大多数患者患有急性(44%)和/或慢性(66%)移植物抗宿主病(GVHD)。尽管两组在传统心血管危险因素方面相匹配,但 alloHCT 幸存者与对照组相比,血小板和红细胞 MV 显著增加。在 alloHCT 幸存者中,有血栓性微血管病既往史的患者红细胞 MV 显著增加。有趣的是,只有接受清髓性预处理的 alloHCT 受者内皮 MV 才显著增加。此外,不同来源的 MV 彼此之间呈正相关。(4) 结论:在 alloHCT 后很长一段时间内,异基因造血细胞移植受者的内皮功能障碍和血栓形成风险增加,与传统心血管危险因素无关。这些病理生理过程的明显协同作用可能与随后心血管疾病的发生密切相关。