Blood-brain barrier disruption and sustained systemic inflammation in individuals with long COVID-associated cognitive impairment.
Chris GreeneRuairi ConnollyDeclan BrennanAoife LaffanEoin O'KeeffeLilia ZaporojanJeffrey O'CallaghanBennett ThomsonEmma ConnollyRuth ArgueIgnacio Martin-LoechesAideen LongCliona Ni CheallaighNiall ConlonColin P DohertyMatthew CampbellPublished in: Nature neuroscience (2024)
Vascular disruption has been implicated in coronavirus disease 2019 (COVID-19) pathogenesis and may predispose to the neurological sequelae associated with long COVID, yet it is unclear how blood-brain barrier (BBB) function is affected in these conditions. Here we show that BBB disruption is evident during acute infection and in patients with long COVID with cognitive impairment, commonly referred to as brain fog. Using dynamic contrast-enhanced magnetic resonance imaging, we show BBB disruption in patients with long COVID-associated brain fog. Transcriptomic analysis of peripheral blood mononuclear cells revealed dysregulation of the coagulation system and a dampened adaptive immune response in individuals with brain fog. Accordingly, peripheral blood mononuclear cells showed increased adhesion to human brain endothelial cells in vitro, while exposure of brain endothelial cells to serum from patients with long COVID induced expression of inflammatory markers. Together, our data suggest that sustained systemic inflammation and persistent localized BBB dysfunction is a key feature of long COVID-associated brain fog.
Keyphrases
- coronavirus disease
- blood brain barrier
- cerebral ischemia
- sars cov
- cognitive impairment
- magnetic resonance imaging
- endothelial cells
- resting state
- respiratory syndrome coronavirus
- white matter
- immune response
- functional connectivity
- cystic fibrosis
- intensive care unit
- computed tomography
- brain injury
- multiple sclerosis
- escherichia coli
- deep learning
- single cell
- liver failure
- hepatitis b virus
- inflammatory response
- extracorporeal membrane oxygenation
- dendritic cells
- vascular endothelial growth factor
- subarachnoid hemorrhage
- diabetic rats