Effects of echinocandins on cytokine/chemokine production by human monocytes activated by infection with Candida glabrata or by lipopolysaccharide

Diagn Microbiol Infect Dis. 2012 Mar;72(3):226-33. doi: 10.1016/j.diagmicrobio.2011.11.004. Epub 2011 Dec 29.

Abstract

Serious Candida glabrata infections, which can be difficult to treat, are often treated with echinocandins. We compared in vitro the effects of high and low concentrations of 3 echinocandins (micafungin [MCF], caspofungin [CAS], and anidulafungin [ANF]), voriconazole (VRC), and amphotericin B (AmB), singly and VRC in combination with MCF, CAS, and ANF, on the production of cytokines/chemokines by human monocyte-derived macrophages (MDM). MDM were activated by infection with C. glabrata or lipopolysaccharide (LPS). Luminex multi-analyte microsphere technology was used for cytokine/chemokine analysis. Concentrations of cytokines/chemokines were significantly elevated following activation by infection or LPS. Treatment with high concentrations of echinocandins, singly or in combination with VRC, was most effective in lowering the elevated cytokine/chemokine levels. This effect occurred only with MDM activated by infection with C. glabrata and not with LPS. Treatment with VRC or AmB alone had little or no effect on cytokine/chemokine levels. In severe C. glabrata infection associated with very high concentrations of dysregulated cytokines/chemokines, echinocandins, singly or in combination with VRC, may decrease cytokine/chemokine concentrations and thus may improve host survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / pharmacology*
  • Candida glabrata / immunology*
  • Candidiasis / immunology
  • Candidiasis / metabolism
  • Chemokines / biosynthesis
  • Cytokines / biosynthesis*
  • Echinocandins / pharmacology*
  • Humans
  • Lipopolysaccharides / immunology*
  • Macrophage Activation / immunology
  • Macrophages / drug effects*
  • Macrophages / immunology*

Substances

  • Antifungal Agents
  • Chemokines
  • Cytokines
  • Echinocandins
  • Lipopolysaccharides