Molinaro Roberto, Pasto Anna, Taraballi Francesca, Giordano Federica, Azzi Jamil A, Tasciotti Ennio, Corbo Claudia
Center for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Nanomaterials (Basel). 2020 Nov 20;10(11):2301. doi: 10.3390/nano10112301.
Recent studies on coronavirus infectious disease 2019 (COVID-19) pathophysiology indicated the cytokine release syndrome induced by the virus as the main cause of mortality. Patients with severe COVID-19 infection present a systemic hyper inflammation that can lead to lung and multi-organ injuries. Among the most recent treatments, corticosteroids have been identified to be effective in mitigating these catastrophic effects. Our group has recently developed leukocyte-derived nanovesicles, termed leukosomes, able to target in vivo the inflamed vasculature associated with pathological conditions including cancer, cardiovascular diseases, and sepsis. Herein, to gain insights on the anti-inflammatory properties of leukosomes, we investigated their ability to reduce uncontrolled inflammation in a lethal model of lipopolysaccharide (LPS)-induced endotoxemia, recapitulating the cytokine storm syndrome observed in COVID-19 infection after encapsulating dexamethasone. Treated animals showed a significant survival advantage and an improved immune response resolution, as demonstrated by a cytokine array analysis of pro- and anti-inflammatory cytokines, chemokines, and other immune-relevant markers. Our results showed that leukosomes enhance the therapeutic activity of dexamethasone and better control the inflammatory response compared to the free drug. Such an approach could be useful for the development of personalized therapies in the treatment of hyperinflammation related to infectious diseases, including the ones caused by COVID-19.
最近关于2019冠状病毒病(COVID-19)病理生理学的研究表明,该病毒诱导的细胞因子释放综合征是导致死亡的主要原因。重症COVID-19感染患者会出现全身炎症反应过度,进而可能导致肺部和多器官损伤。在最新的治疗方法中,已确定皮质类固醇在减轻这些灾难性影响方面有效。我们团队最近开发了一种白细胞衍生的纳米囊泡,称为白细胞体,它能够在体内靶向与包括癌症、心血管疾病和败血症在内的病理状况相关的炎症血管。在此,为了深入了解白细胞体的抗炎特性,我们研究了在封装地塞米松后,其在脂多糖(LPS)诱导的内毒素血症致死模型中减少失控性炎症的能力,该模型模拟了COVID-19感染中观察到的细胞因子风暴综合征。通过对促炎和抗炎细胞因子、趋化因子及其他免疫相关标志物进行细胞因子阵列分析表明,接受治疗的动物显示出显著的生存优势和免疫反应缓解情况得到改善。我们的结果表明,与游离药物相比,白细胞体增强了地塞米松的治疗活性,并能更好地控制炎症反应。这种方法可能有助于开发针对与传染病相关的炎症过度,包括由COVID-19引起的炎症过度的个性化治疗方案。