期刊
VIRUSES-BASEL
卷 13, 期 8, 页码 -出版社
MDPI
DOI: 10.3390/v13081597
关键词
PAI-1; orthohantavirus; hantavirus; principal component analysis; plasminogen activation; cytokines; ECMO; uPA; correlation; pathogenesis; cell barrier function; co-infection
类别
资金
- NIH National Center for Research Resources
- National Center for Advancing Translational Sciences [UL1TR001449]
- UNM Department of Pathology
Pathogenic New World orthohantaviruses can cause hantavirus cardiopulmonary syndrome (HCPS) in humans, with high levels of inflammatory mediators present in patients. A study analyzing immune responses in HCPS cases due to Sin Nombre orthohantavirus found significantly elevated levels of proinflammatory cytokines and PAI-1 in end-stage cases, with total uPA higher in decedents compared to survivors. Bacterial co-infection may influence the etiology and outcome of immune response, with a robust proinflammatory immune response correlated with dysregulated inflammation and mortality in some cases.
Pathogenic New World orthohantaviruses cause hantavirus cardiopulmonary syndrome (HCPS), a severe immunopathogenic disease in humans manifested by pulmonary edema and respiratory distress, with case fatality rates approaching 40%. High levels of inflammatory mediators are present in the lungs and systemic circulation of HCPS patients. Previous studies have provided insights into the pathophysiology of HCPS. However, the longitudinal correlations of innate and adaptive immune responses and disease outcomes remain unresolved. This study analyzed serial immune responses in 13 HCPS cases due to Sin Nombre orthohantavirus (SNV), with 11 severe cases requiring extracorporeal membrane oxygenation (ECMO) treatment and two mild cases. We measured viral load, levels of various cytokines, urokinase plasminogen activator (uPA), and plasminogen activator inhibitor-1 (PAI-1). We found significantly elevated levels of proinflammatory cytokines and PAI-1 in five end-stage cases. There was no difference between the expression of active uPA in survivors' and decedents' cases. However, total uPA in decedents' cases was significantly higher compared to survivors'. In some end-stage cases, uPA was refractory to PAI-1 inhibition as measured by zymography, where uPA and PAI-1 were strongly correlated to lymphocyte counts and IFN-gamma. We also found bacterial co-infection influencing the etiology and outcome of immune response in two cases. Unsupervised Principal Component Analysis and hierarchical cluster analyses resolved separate waves of correlated immune mediators expressed in one case patient due to a sequential co-infection of bacteria and SNV. Overall, a robust proinflammatory immune response, characterized by an imbalance in T helper 17 (Th17) and regulatory T-cells (Treg) subsets, was correlated with dysregulated inflammation and mortality. Our sample size is small; however, the core differences correlated to survivors and end-stage HCPS are instructive.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据