Peripheral white blood cell patterns in children with hydrocephalus as a response to ventriculo-peritoneal shunt

Bartosz Polis1, Krzysztof Zeman2, Krzysztof Zakrzewski1

  • 1Department of Neurosurgery, Polish Mother's Memorial Hospital- Research Institute in Lodz, Lodz, Poland.

Plos One
|August 9, 2024
PubMed

Insights

Shunt infections from S. epidermidis in children with hydrocephalus trigger an early immune response. Cerebrospinal fluid changes, including protein levels, precede white blood cell increases, with monocytes aiding recovery.

Area of Science:

  • Neuroscience
  • Immunology
  • Pediatrics

Background:

  • Shunt infection is a common complication in pediatric hydrocephalus treatment.
  • Pathogen invasion route influences the central nervous system (CNS) immune response.
  • Staphylococcus epidermidis (S. epidermidis) is a frequent cause of shunt infections.

Purpose of the Study:

  • To analyze the immune response to S. epidermidis shunt infections in children with hydrocephalus.
  • To correlate laboratory findings with immune system activation.
  • To understand the role of specific immune cells and cytokines in the CNS response.

Main Methods:

  • Analysis of white blood cell (WBC) counts (neutrophils, monocytes, lymphocytes) in peripheral blood.
  • Examination of cerebrospinal fluid (CSF) parameters: pleocytosis, protein, and glucose levels.
  • Measurement of selected interleukins (IL-6, CXCL8/IL-8, CCL3/MIP-1a) in CSF.

Main Results:

  • Significant increase in all WBC lines upon admission in infected patients.
  • Elevated protein levels in CSF were the earliest indicator of infection.
  • CSF humoral immune response and cytokine levels peaked post-pathogen clearance, with monocytes playing a key role in normalization.

Conclusions:

  • S. epidermidis shunt infection elicits an early peripheral immune response.
  • In CNS infections, CSF immune markers like protein elevation can precede pleocytosis.
  • Monocytes are crucial for resolving inflammation and normalizing CSF parameters post-infection.