Sterile Cerebrospinal Fluid Culture at Cryptococcal Meningitis Diagnosis Is Associated with High Mortality

Caleb P Skipper1,2, Katherine Huppler Hullsiek3, Anna Stadelman3

  • 1Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.

Insights

Sterile cerebrospinal fluid (CSF) cultures in HIV-associated cryptococcal meningitis patients do not predict better outcomes. Despite favorable immune markers, mortality in sterile culture groups was similar to those with higher fungal burdens.

Area of Science:

  • Infectious Diseases
  • Immunology
  • Neuroscience

Background:

  • Cryptococcus is a major cause of AIDS-related meningitis in sub-Saharan Africa.
  • The significance of sterile cerebrospinal fluid (CSF) cultures in cryptococcal meningitis (CM) patients diagnosed via CSF cryptococcal antigen (CrAg) is not well understood.

Purpose of the Study:

  • To investigate the clinical implications of sterile CSF cultures in HIV-positive patients with first-episode CM.
  • To compare clinical characteristics, CSF immune profiles, and mortality between patients with sterile and non-sterile CSF cultures.

Main Methods:

  • Prospective enrollment of 765 HIV-positive Ugandan patients with first-episode CM.
  • Treatment with amphotericin-based induction therapy.
  • Grouping participants by tertiles of baseline CSF quantitative Cryptococcus culture burden and comparing outcomes.

Main Results:

  • 7% of patients had sterile CSF cultures despite positive CSF CrAg.
  • Sterile culture group had higher CD4 counts, lower CSF opening pressures, and more frequent ART use.
  • 18-week mortality was 47% in the sterile group vs. 35-56% in non-sterile groups (p < 0.001).
  • Sterile group showed elevated CSF IFN-γ, IFN-α, IL-6, IL-17, G-CSF, GM-CSF, and CXCL2.

Conclusions:

  • Sterile CSF cultures in CM patients, despite favorable immune profiles, are associated with unexpected mortality rates similar to higher fungal burdens.
  • Findings challenge the traditional view linking higher fungal burden to increased mortality.
  • Results support a damage-response framework model in CM pathogenesis.

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