Unit of Clinical Biochemistry, Section of Biochemistry and Biotechnology, Department of Biomolecular Sciences -DISB, University of Urbino Carlo Bo, Via A. Saffi, 2, 61029, Urbino, Italy.
Institute of Clinical Biochemistry, Clinical Molecular Medicine and Clinical Laboratory Medicine, Department of Biomedicine, Neurosciences and Advanced Diagnostics, BiND, University of Palermo, Via del Vespro, 90127, Palermo, Italy.
Crit Care. 2022 Aug 30;26(1):260. doi: 10.1186/s13054-022-04138-2.
Histone proteins are physiologically involved in DNA packaging and gene regulation but are extracellularly released by neutrophil/monocyte extracellular traps and mediate thrombo-inflammatory pathways, associated to the severity of many human pathologies, including bacterial/fungal sepsis and COVID-19. Prominent and promising laboratory features in classic and viral sepsis emphasize monocyte distribution width (MDW), due to its ability to distinguish and stratify patients at higher risk of critical conditions or death. No data are available on the roles of histones as MDW modifiers.
Comparison of MDW index was undertaken by routine hematology analyzer on whole blood samples from patients with COVID-19 and Sepsis. The impact of histones on the MDW characteristics was assessed by the in vitro time-dependent treatment of healthy control whole blood with histones and histones plus lipopolysaccharide to simulate viral and classical sepsis, respectively.
We demonstrated the breadth of early, persistent, and significant increase of MDW index in whole blood from healthy subject treated in vitro with histones, highlighting changes similar to those found in vivo in classic and viral sepsis patients. These findings are mechanistically associated with the histone-induced modifications of cell volume, cytoplasmic granularity and vacuolization, and nuclear structure alterations of the circulating monocyte population.
Histones may contribute to the pronounced and persistent monocyte alterations observed in both acute classical and viral sepsis. Assessment of the biological impact of circulating histone released during COVID-19 and sepsis on these blood cells should be considered as key factor modulating both thrombosis and inflammatory processes, as well as the importance of neutralization of their cytotoxic and procoagulant activities by several commercially available drugs (e.g., heparins and heparinoids).
组蛋白在生理上参与 DNA 包装和基因调控,但通过中性粒细胞/单核细胞细胞外陷阱释放到细胞外,并介导血栓炎症途径,与许多人类疾病的严重程度相关,包括细菌/真菌感染性败血症和 COVID-19。经典和病毒性败血症中的显著和有前途的实验室特征强调单核细胞分布宽度(MDW),因为它能够区分和分层具有更高危重症或死亡风险的患者。尚无关于组蛋白作为 MDW 调节剂作用的数据。
通过常规血液学分析仪对 COVID-19 和败血症患者的全血样本进行 MDW 指数比较。通过用组蛋白和组蛋白加脂多糖分别模拟病毒和经典败血症,在体外对健康对照全血进行时间依赖性处理,评估组蛋白对 MDW 特征的影响。
我们证明了在体外用组蛋白处理的健康受试者的全血中 MDW 指数早期、持续和显著增加的广泛性,突出了与经典和病毒性败血症患者体内发现的变化相似的变化。这些发现与组蛋白诱导的循环单核细胞群体的细胞体积、细胞质颗粒和空泡化以及核结构改变的修饰有关。
组蛋白可能有助于急性经典和病毒性败血症中观察到的明显和持续的单核细胞改变。在 COVID-19 和败血症期间释放的循环组蛋白对这些血细胞的生物学影响的评估应被视为调节血栓形成和炎症过程的关键因素,以及中和其细胞毒性和促凝活性的重要性由几种市售药物(例如肝素和肝素类药物)。