Abstract

BackgroundTick-borne encephalitis (TBE) is a clinically variable but potentially severe Flavivirus infection, with the outcome strongly dependent on secondary immunopathology. Neutrophils are present in cerebrospinal fluid (CSF) of TBE patients, but their pathogenetic role remains unknown. In animal models, neutrophils contributed both to the Flavivirus entry into central nervous system (CNS) and to the control of the encephalitis, which we attempted to evaluate in human TBE.MethodsWe analyzed records of 240 patients with TBE presenting as meningitis (n = 110), meningoencephalitis (n = 114) or meningoencephalomyelitis (n = 16) assessing CSF neutrophil count on admission and at follow-up 2 weeks later, and their associations with other laboratory and clinical parameters. We measured serum and CSF concentrations of Th17-type cytokines (interleukin-17A, IL-17F, IL-22) and chemokines attracting neutrophils (IL-8, CXCL1, CXCL2) in patients with TBE (n = 36 for IL-8, n = 15 for other), with non-TBE aseptic meningitis (n = 6) and in non-meningitis controls (n = 7), using commercial ELISA assays. The results were analyzed with non-parametric tests with p < 0.05 considered as significant.ResultsOn admission, neutrophils were universally present in CSF constituting 25% (median) of total pleocytosis, but on follow-up, they were absent in most of patients (58%) and scarce (< 10%) in 36%. CSF neutrophil count did not correlate with lymphocyte count and blood-brain barrier integrity, did not differ between meningitis and meningoencephalitis, but was higher in meningoencephalomyelitis patients. Prolonged presence of neutrophils in follow-up CSF was associated with encephalitis and neurologic sequelae. All the studied cytokines were expressed intrathecally, with IL-8 having the highest CSF concentration index. Additionally, IL-17A concentration was significantly increased in serum. IL-17F and CXCL1 CSF concentrations correlated with neutrophil count and CXCL1 concentration was higher in patients with encephalitis.ConclusionsThe neutrophil CNS infiltrate does not correlate directly with TBE severity, but is associated with clinical features like myelitis, possibly being involved in its pathogenesis. Th17 cytokine response is present in TBE, especially intrathecally, and contributes to the CNS neutrophilic inflammation. IL-8 and CXCL1 may be chemokines directly responsible for the neutrophil migration.

Highlights

  • Tick-borne encephalitis (TBE) is a clinically variable but potentially severe Flavivirus infection, with the outcome strongly dependent on secondary immunopathology

  • The cerebrospinal fluid (CSF) neutrophil fraction was similar to previously described by Mickiené et al in TBE, and somewhat lower than that reported in West Nile virus (WNV)-infected patient groups, which was 41% in meningitis and 45% in encephalitis according to Tyler et al, and 50% decreasing to 37% over 3 days since onset according to Rawal et al [4, 19, 48]

  • The authors hypothesized that neutrophils initiate the protective accumulation of mononuclear cells within central nervous system (CNS) by first contributing to blood/brain barrier (BBB) disruption and by secreting chemokines including CCL3, CCL4, CXCL9, CXCL10, and CXCL11 [25], some of which have been detected in TBE CSF [13, 49]

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Summary

Introduction

Tick-borne encephalitis (TBE) is a clinically variable but potentially severe Flavivirus infection, with the outcome strongly dependent on secondary immunopathology. The European TBEV subtype frequently causes a mild flu-like disease, but in some cases, it is able to penetrate the blood/brain barrier (BBB) causing the second, neurologic phase of the disease, which may take a severe course and leave permanent neurologic sequelae [1,2,3,4,5]. Both the animal models and the results of human studies point to the involvement of the host immune/inflammatory response in the pathogenesis. Mouse strains more sensitive to TBEV present with a higher expression of the pro-inflammatory cytokines and chemokines during encephalitis [16]

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