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Neurological Manifestations of COVID-19 Feature T Cell Exhaustion and Dedifferentiated Monocytes in Cerebrospinal Fluid

Patients suffering from Coronavirus disease 2019 (COVID-19) can develop neurological sequelae, such as headache and neuroinflammatory or cerebrovascular disease. These conditions—termed here as Neuro-COVID—are more frequent in patients with severe COVID-19. To understand the etiology of these neurol...

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Detalles Bibliográficos
Autores principales: Heming, Michael, Li, Xiaolin, Räuber, Saskia, Mausberg, Anne K., Börsch, Anna-Lena, Hartlehnert, Maike, Singhal, Arpita, Lu, I-Na, Fleischer, Michael, Szepanowski, Fabian, Witzke, Oliver, Brenner, Thorsten, Dittmer, Ulf, Yosef, Nir, Kleinschnitz, Christoph, Wiendl, Heinz, Stettner, Mark, Meyer zu Hörste, Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831653/
https://www.ncbi.nlm.nih.gov/pubmed/33382973
http://dx.doi.org/10.1016/j.immuni.2020.12.011
Descripción
Sumario:Patients suffering from Coronavirus disease 2019 (COVID-19) can develop neurological sequelae, such as headache and neuroinflammatory or cerebrovascular disease. These conditions—termed here as Neuro-COVID—are more frequent in patients with severe COVID-19. To understand the etiology of these neurological sequelae, we utilized single-cell sequencing and examined the immune cell profiles from the cerebrospinal fluid (CSF) of Neuro-COVID patients compared with patients with non-inflammatory and autoimmune neurological diseases or with viral encephalitis. The CSF of Neuro-COVID patients exhibited an expansion of dedifferentiated monocytes and of exhausted CD4(+) T cells. Neuro-COVID CSF leukocytes featured an enriched interferon signature; however, this was less pronounced than in viral encephalitis. Repertoire analysis revealed broad clonal T cell expansion and curtailed interferon response in severe compared with mild Neuro-COVID patients. Collectively, our findings document the CSF immune compartment in Neuro-COVID patients and suggest compromised antiviral responses in this setting.