Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK.
Int J Mol Sci. 2024 Jun 27;25(13):7027. doi: 10.3390/ijms25137027.
There is growing evidence that inflammation impairs erythrocyte structure and function. We assessed the impact of mild systemic inflammation on erythrocyte fragility in three different settings. In order to investigate causation, erythrocyte osmotic fragility was measured in mice challenged with a live attenuated bacterial strain to induce low-grade systemic inflammation; a significant increase in erythrocyte osmotic fragility was observed. To gather evidence that systemic inflammation is associated with erythrocyte fragility in humans, two observational studies were conducted. First, using a retrospective study design, the relationship between reticulocyte-based surrogate markers of haemolysis and high-sensitivity C-reactive protein was investigated in 9292 healthy participants of the UK Biobank project. Secondly, we prospectively assessed the relationship between systemic inflammation (measured by the urinary neopterin/creatinine ratio) and erythrocyte osmotic fragility in a mixed population (n = 54) of healthy volunteers and individuals with long-term medical conditions. Both human studies were in keeping with a relationship between inflammation and erythrocyte fragility. Taken together, we conclude that mild systemic inflammation increases erythrocyte fragility and may contribute to haemolysis. Further research is needed to assess the molecular underpinnings of this pathway and the clinical implications in inflammatory conditions.
越来越多的证据表明炎症会损害红细胞的结构和功能。我们在三种不同情况下评估了轻度全身炎症对红细胞脆性的影响。为了探究病因,我们在感染减毒活菌以引起低度全身炎症的小鼠中测量了红细胞渗透脆性;观察到红细胞渗透脆性显著增加。为了收集全身炎症与人类红细胞脆性相关的证据,我们进行了两项观察性研究。首先,使用回顾性研究设计,在英国生物银行项目的 9292 名健康参与者中,研究了网织红细胞为基础的溶血替代标志物与高敏 C 反应蛋白之间的关系。其次,我们前瞻性评估了混合人群(健康志愿者和长期患病个体,n=54)中全身炎症(通过尿中新蝶呤/肌酐比测量)与红细胞渗透脆性之间的关系。这两项人类研究都表明炎症与红细胞脆性之间存在关联。综上所述,我们得出结论,轻度全身炎症会增加红细胞脆性,并可能导致溶血。需要进一步研究以评估该途径的分子基础及其在炎症情况下的临床意义。