Pulmonary SARS-CoV-2 infection leads to para-infectious immune activation in the brain.
Dunai C., Hetherington C., Boardman SA., Clark JJ., Sharma P., Subramaniam K., Tharmaratnam K., Needham EJ., Williams R., Huang Y., Wood GK., Collie C., Fower A., Fox H., Ellul MA., Held M., Egbe FN., Griffiths M., Solomon T., Breen G., Kipar A., Cavanagh J., Irani SR., Vincent A., Stewart JP., Taams LS., Menon DK., Michael BD.
Neurological complications, including encephalopathy and stroke, occur in a significant proportion of COVID-19 cases but viral protein is seldom detected in the brain parenchyma. To model this situation, we developed a novel low-inoculum K18-hACE2 mouse model of SARS-CoV-2 infection during which active viral replication was consistently seen in mouse lungs but not in the brain. We found that several mediators previously associated with encephalopathy in clinical samples were upregulated in the lung, including CCL2, and IL-6. In addition, several inflammatory mediations, including CCL4, IFNγ, IL-17A, were upregulated in the brain, associated with microglial reactivity. Parallel in vitro experiments demonstrated that the filtered supernatant from SARS-CoV-2 virion exposed brain endothelial cells induced activation of uninfected microglia. This model successfully recreates SARS-CoV-2 virus-associated para-infectious brain inflammation which can be used to study the pathophysiology of the neurological complications and the identification of potential immune targets for treatment.