Akademik Veri Yönetim Sistemi
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE, cilt.78, sa.3-4, ss.136-144, 2025 (SCI-Expanded)
Background and purpose - High titers of anti-SARS-CoV-2 immunoglobulin G (IgG) have been reported in cerebrospinal fluid (CSF) samples of patients with COVID-19, but the data are limited. Our purpose is to report the clinical features and CSF findings of patients with neurologic symptoms in the pandemic era, and to discuss the origin and importance of anti-SARS-CoV-2 IgG in CSF. Methods - The data of 100 patients hospitalized in neurology inpatient clinics and tested for anti-SARS-CoV-2 IgG antibodies in CSF samples, between May 2021 and March 2022, were evaluated in a retrospective manner. Demographic features, presence of coronavirus disease 2019 (COVID-19) and/ or COVID-19 history, vaccination, vaccine type, and neurologic diagnoses were noted. CSF and serum anti-SARS-CoV-2 antibody ratio (AR) were assessed using a Euroimmun ELISA assay. CSF cytology, CSF protein level, oligoclonal band, IgG index, and albumin quotient (QAlb) were analyzed and compared between CSFAR positive and negative groups. Results - QAlb and CSF protein levels were higher in the CSF anti-SARS-CoV-2 AR-positive group compared with CSF anti-SARSCoV-2 AR-negative group (p<0.05). IgG index, CSF cytology, and oligoclonal band (OCB) types did not differ between the groups. Seventy-three percent of patients had OCB type-1. CSF anti-SARS-CoV-2 AR was correlated with serum anti-SARS-CoV-2 AR, Qalb, and CSF protein level, as well as COVID-19 and/or COVID-19 history and vaccination. Conclusion - Anti-SARS-CoV-2 antibodies in CSF seem to be related to a past immunization or a pre-existing cross reactive immunity and passive diffusion through a disrupted blood-brain-barrier, but not to an intrathecal antibody synthesis.