4.7 Article

Antibody Responses to Severe Acute Respiratory Syndrome Coronavirus 2 in the Serum and Cerebrospinal Fluid of Patients With Coronavirus Disease 2019 and Neurological Symptoms

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 225, Issue 6, Pages 965-970

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab153

Keywords

COVID-19; SARS-CoV-2; serology; CSF; IgG; neurological symptoms

Funding

  1. Swedish Research Council [2018-02532, 201402569, 2014-07606, 2017-00968, 2018-02569]
  2. Open Medicine Foundation
  3. SciLife/KWA
  4. Swedish government
  5. Swedish Society for Medical Research
  6. Wallenberg Foundations
  7. European Research Council [681712]
  8. Swedish State Support for Clinical Research [ALFGBG-720931]
  9. Alzheimer Drug Discovery Foundation [2018092016862]
  10. European Union [860197, 874735]
  11. UK Dementia Research Institute at UCL
  12. Knut and Alice Wallenberg Foundation
  13. Science for Life Laboratory Uppsala

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Patients with coronavirus disease 2019 and neurological symptoms have immunoglobulin G against SARS-CoV-2 in both serum and cerebrospinal fluid, and the levels of IgG are associated with disease severity. Cerebrospinal fluid antibodies have the highest predictive value for central nervous system damage markers.
Patients with coronavirus disease 2019 and neurological symptoms had immunoglobulin G against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) S/S1 protein in both serum (81%) and cerebrospinal fluid (56%). All patients with elevated markers of central nervous system damage also had immunoglobulin G against SARS-CoV-2 in cerebrospinal fluid. Antibody responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in serum and cerebrospinal fluid (CSF) samples from 16 patients with coronavirus disease 2019 and neurological symptoms were assessed using 2 independent methods. Immunoglobulin G (IgG) specific for the virus spike protein was found in 81% of patients in serum and in 56% in CSF. SARS-CoV-2 IgG in CSF was observed in 2 patients with negative serological findings. Levels of IgG in both serum and CSF were associated with disease severity (P < .05). All patients with elevated markers of central nervous system damage in CSF also had CSF antibodies (P = .002), and CSF antibodies had the highest predictive value for neuronal damage markers of all tested clinical variables.

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