Chemokine and Cytokine Cascade Caused by Skewing of the Th1-Th2 Balance Is Associated with High Intracranial Pressure in HIV-Associated Cryptococcal Meningitis

Mediators Inflamm. 2019 Dec 31:2019:2053958. doi: 10.1155/2019/2053958. eCollection 2019.

Abstract

Purpose: Serum cytokines/chemokines play important roles in cryptococcal meningitis, but it is unclear whether cytokines/chemokines in cerebrospinal fluid (CSF) contribute to high intracranial pressure (HICP) in HIV-associated cryptococcal meningitis (HCM).

Methods: CSF cytokines/chemokines were assayed in 17 HIV-uninfected patients, 26 HIV-infected patients without CNS infection, and 39 HCM patients at admission. Principal component analysis and correlation and logistic regression analyses were used to assess the relationships between these parameters.

Results: The CSF Th1, Th2, and macrophage cytokines showed an obvious increase in HCM patients as compared to the HIV-uninfected patients and HIV-infected patients without CNS infection. CSF IL-6, GM-CSF, and IL-8 were positively correlated with CSF fungal burden. Serum CD4 count, CSF Th1 cytokines (TNF-α, TNF-β, IL-12, IL-1β, IL-12, IL-1α, TNF-α, TNF-β, IL-12, IL-1γ, and IL-12) and Th2 cytokines (IL-4 and IL-10) contribute to HICP.

Conclusion: Overall, the present findings indicated that both pro- and anti-inflammatory cytokines of Th1, Th2, and macrophage origin contributed to the development of HCM. Specifically, the chemokine and cytokine cascade caused by skewing of the Th1-Th2 balance and reduced CD4 count were found to be important contributors to HICP. Summary. Our research suggested that chemokine and cytokine cascade caused by skewing of the Th1-Th2 balance in HIV-infected patients played more important role than Cryptococcus numbers and size in CSF on the development of high intracranial pressure in HIV-associated cryptococcal meningitis, providing a new understanding of mechanisms of HCM.

MeSH terms

  • Adult
  • CD4 Lymphocyte Count
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Female
  • HIV Infections / genetics
  • HIV Infections / metabolism*
  • HIV Infections / physiopathology*
  • Humans
  • Intracranial Pressure / genetics
  • Intracranial Pressure / physiology*
  • Male
  • Meningitis, Cryptococcal / genetics
  • Meningitis, Cryptococcal / metabolism*
  • Meningitis, Cryptococcal / physiopathology*
  • Middle Aged
  • Th1-Th2 Balance / genetics
  • Th1-Th2 Balance / physiology*

Substances

  • Chemokines
  • Cytokines