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Correlation between Blood and CSF Compartment Cytokines and Chemokines in Subjects with Cryptococcal Meningitis

  • Elizabeth C Okafor
  • , Katherine H Hullsiek
  • , Darlisha A Williams
  • , James E Scriven
  • , Joshua Rhein
  • , Henry W Nabeta
  • , Abdu K Musubire
  • , Radha Rajasingham
  • , Conrad Muzoora
  • , Charlotte Schutz
  • , Graeme Meintjes
  • , David B Meya
  • , David R Boulware

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND: Though peripheral blood is a crucial sample to study immunology, it is unclear whether the immune environment in the peripheral vasculature correlates with that at the end-organ site of infection. Using cryptococcal meningitis as a model, we investigated the correlation between serum and cerebrospinal fluid biomarkers over time.

METHODS: We analyzed the cerebrospinal fluid and serum of 160 subjects presenting with first episode cryptococcal meningitis for soluble cytokines and chemokines measured by Luminex assay. Specimens were collected at meningitis diagnosis, 1-week, and 2-week post cryptococcal diagnosis. We compared paired samples by Spearman's correlation and the p value was set at <0.01.

RESULTS: Of the 21 analytes tested at baseline, there was no correlation detected between nearly all analytes. A weak negative correlation was found between serum and cerebrospinal fluid levels of interferon-gamma (Rho = -0.214; p = .007) and interleukin-4 (Rho = -0.232; p = .003). There was no correlation at 1-week post cryptococcal diagnosis. However, at 2-week post cryptococcal diagnosis, there was a weak positive correlation of granulocyte-macrophage colony-stimulating factor levels (Rho = 0.25; p = .007) in serum and cerebrospinal fluid. No cytokine or chemokine showed consistent correlation overtime.

CONCLUSION: Based on our analysis of 21 biomarkers, serum and cerebrospinal fluid immune responses do not correlate. There appears to be a distinct immune environment in terms of soluble biomarkers in the vasculature versus end-organ site of infection. While this is a model of HIV-related cryptococcal meningitis, we postulate that assuming the blood compartment is representative of the immune function at the end-organ site of infection may not be appropriate.

Original languageEnglish
Pages (from-to)8818044
JournalMediators of Inflammation
Volume2020
DOIs
Publication statusPublished - 2020

Bibliographical note

Copyright © 2020 Elizabeth C. Okafor et al.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adult
  • Biomarkers/blood
  • Chemokines/blood
  • Cytokines/blood
  • Female
  • Granulocyte Colony-Stimulating Factor/metabolism
  • HIV Infections/complications
  • Humans
  • Immune System
  • Immunocompromised Host
  • Interferon-gamma/blood
  • Interleukin-4/blood
  • Male
  • Meningitis, Cryptococcal/blood
  • Reproducibility of Results

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