Up-regulation of Borrelia-specific IL-4- and IFN-gamma-secreting cells in cerebrospinal fluid from children with Lyme neuroborreliosis

Int Immunol. 2005 Oct;17(10):1283-91. doi: 10.1093/intimm/dxh304.

Abstract

The clinical course and outcome of several infectious diseases are dependent on the type of immune response elicited against the pathogen. In adults with neuroborreliosis (NB), a type 1 response with high production of Borrelia-specific IFN-gamma, but no IL-4, has been reported. Since children have a more benign course of NB than adults, we wanted to investigate type 1 and type 2 responses in children with NB. Cerebrospinal fluid (CSF) and blood were collected from children during the acute stage of 'confirmed NB' (n = 34), 'possible NB' (n = 30) and 'non-NB' (n = 10). The number of Borrelia-specific IL-4- and IFN-gamma-secreting cells was measured by enzyme-linked immunospot assay. Borrelia-specific secretion of both IL-4 and IFN-gamma was increased in CSF in confirmed (P < 0.05) and possible (P < 0.01) NB, when compared with non-NB controls. Furthermore, children with NB had significantly higher Borrelia-specific IL-4 secretion in CSF than an adult reference material with NB (P < 0.05). There were no differences in cytokine secretion in relation to onset or recovery of neurological symptoms. Since IL-4 is known to down-regulate the pro-inflammatory and possibly harmful effects of prolonged IFN-gamma responses, the prominent IL-4 response observed in the central nervous system compartment might contribute to the more benign disease course seen in children with Lyme NB.

MeSH terms

  • Adolescent
  • Adult
  • Borrelia burgdorferi / immunology*
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Interferon-gamma / metabolism*
  • Interleukin-4 / metabolism*
  • Lyme Neuroborreliosis / cerebrospinal fluid*
  • Lyme Neuroborreliosis / immunology*
  • Lyme Neuroborreliosis / pathology
  • Lymphocyte Count
  • Lymphocytes / immunology
  • Lymphocytes / metabolism
  • Male
  • Prospective Studies
  • Up-Regulation / immunology*

Substances

  • Interleukin-4
  • Interferon-gamma