CSF Biomarkers in COVID-19 Associated Encephalopathy and Encephalitis Predict Long-Term Outcome.

COVID-19 SARS-CoV-2 encephalitis encephalopathy inflammatory cytokines neuro-COVID neurofilaments neuronal antibodies

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 30 01 2022
accepted: 18 03 2022
entrez: 28 4 2022
pubmed: 29 4 2022
medline: 30 4 2022
Statut: epublish

Résumé

Patients with coronavirus disease 2019 (COVID-19) frequently develop acute encephalopathy and encephalitis, but whether these complications are the result from viral-induced cytokine storm syndrome or anti-neural autoimmunity is still unclear. In this study, we aimed to evaluate the diagnostic and prognostic role of CSF and serum biomarkers of inflammation (a wide array of cytokines, antibodies against neural antigens, and IgG oligoclonal bands), and neuroaxonal damage (14-3-3 protein and neurofilament light [NfL]) in patients with acute COVID-19 and associated neurologic manifestations (neuro-COVID). We prospectively included 60 hospitalized neuro-COVID patients, 25 (42%) of them with encephalopathy and 14 (23%) with encephalitis, and followed them for 18 months. We found that, compared to healthy controls (HC), neuro-COVID patients presented elevated levels of IL-18, IL-6, and IL-8 in both serum and CSF. MCP1 was elevated only in CSF, while IL-10, IL-1RA, IP-10, MIG and NfL were increased only in serum. Patients with COVID-associated encephalitis or encephalopathy had distinct serum and CSF cytokine profiles compared with HC, but no differences were found when both clinical groups were compared to each other. Antibodies against neural antigens were negative in both groups. While the levels of neuroaxonal damage markers, 14-3-3 and NfL, and the proinflammatory cytokines IL-18, IL-1RA and IL-8 significantly associated with acute COVID-19 severity, only the levels of 14-3-3 and NfL in CSF significantly correlated with the degree of neurologic disability in the daily activities at 18 months follow-up. Thus, the inflammatory process promoted by SARS-CoV-2 infection might include blood-brain barrier disruption in patients with neurological involvement. In conclusion, the fact that the levels of pro-inflammatory cytokines do not predict the long-term functional outcome suggests that the prognosis is more related to neuronal damage than to the acute neuroinflammatory process.

Identifiants

pubmed: 35479062
doi: 10.3389/fimmu.2022.866153
pmc: PMC9035899
doi:

Substances chimiques

Biomarkers 0
Cytokines 0
Interleukin 1 Receptor Antagonist Protein 0
Interleukin-18 0
Interleukin-8 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

866153

Informations de copyright

Copyright © 2022 Guasp, Muñoz-Sánchez, Martínez-Hernández, Santana, Carbayo, Naranjo, Bolós, Framil, Saiz, Balasa, Ruiz-García, Sánchez-Valle and The Barcelona Neuro-COVID Study Group.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Mar Guasp (M)

Neuroimmunology Program, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.
Centro de Investigación Biomédica en Red, Enfermedades Raras (CIBERER), Madrid, Spain.

Guillermo Muñoz-Sánchez (G)

Immunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic, Barcelona, Spain.

Eugenia Martínez-Hernández (E)

Neuroimmunology Program, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.

Daniel Santana (D)

Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.

Álvaro Carbayo (Á)

Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.

Laura Naranjo (L)

Immunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic, Barcelona, Spain.

Uma Bolós (U)

Immunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic, Barcelona, Spain.

Mario Framil (M)

Department of Immunology, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.

Albert Saiz (A)

Neuroimmunology Program, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.

Mircea Balasa (M)

Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.
Alzheimer's Disease and Other Cognitive Disorders Unit, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.

Raquel Ruiz-García (R)

Neuroimmunology Program, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Immunology Department, Centre Diagnòstic Biomèdic, Hospital Clínic, Barcelona, Spain.

Raquel Sánchez-Valle (R)

Neurology Service, Hospital Clinic de Barcelona, Barcelona, Spain.
Alzheimer's Disease and Other Cognitive Disorders Unit, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.

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