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.

Highlights

  • HIV-associated cryptococcal meningitis (HCM) is a leading cause of mortality in AIDS patients, especially in patients in low-resource settings [1, 2]

  • HIV-associated immune reconstitution inflammatory syndrome (IRIS), which is characterized by an exaggerated inflammatory response in a subset of patients occurred after the initiation of antiretroviral therapy (ART) [6, 7]

  • We explored the mechanism of high intracranial pressure (HICP) in HCM patients by assessing their cerebrospinal fluid (CSF) cytokine/chemokine profile

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Summary

Introduction

HIV-associated cryptococcal meningitis (HCM) is a leading cause of mortality (with a mortality rate of 30-50%) in AIDS patients, especially in patients in low-resource settings [1, 2]. High intracranial pressure (HICP) is one of the important risk factors for mortality in HCM patients [3, 4]. HICP may present as the primary clinical manifestation in untreated HCM patients and in patients who have undergone antifungal therapy for a period of time [3, 5]. HICP is considered as a paradoxical clinical manifestation in HCM patients. HIV-associated immune reconstitution inflammatory syndrome (IRIS), which is characterized by an exaggerated inflammatory response in a subset of patients occurred after the initiation of antiretroviral therapy (ART) [6, 7]. The mechanisms underlying the development of HICP are complicated and debatable; further investigation is required to clarify the mechanisms

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