Two independent killing mechanisms of Candida albicans by human neutrophils: evidence from innate immunity defects

Blood. 2014 Jul 24;124(4):590-7. doi: 10.1182/blood-2014-01-551473. Epub 2014 Jun 19.

Abstract

Invasive fungal infections, accompanied by high rates of mortality, represent an increasing problem in medicine. Neutrophils are the major effector immune cells in fungal killing. Based on studies with neutrophils from patients with defined genetic defects, we provide evidence that human neutrophils use 2 distinct and independent phagolysosomal mechanisms to kill Candida albicans. The first mechanism for the killing of unopsonized C albicans was found to be dependent on complement receptor 3 (CR3) and the signaling proteins phosphatidylinositol-3-kinase and caspase recruitment domain-containing protein 9 (CARD9), but was independent of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity. The second mechanism for the killing of opsonized C albicans was strictly dependent on Fcγ receptors, protein kinase C (PKC), and reactive oxygen species production by the NADPH oxidase system. Each of the 2 pathways of Candida killing required Syk tyrosine kinase activity, but dectin-1 was dispensable for both of them. These data provide an explanation for the variable clinical presentation of fungal infection in patients suffering from different immune defects, including dectin-1 deficiency, CARD9 deficiency, or chronic granulomatous disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Candida albicans / growth & development
  • Candida albicans / immunology*
  • Candidiasis / immunology
  • Candidiasis / microbiology
  • Candidiasis / prevention & control*
  • Cells, Cultured
  • Humans
  • Immunity, Innate / immunology*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Lectins, C-Type / antagonists & inhibitors
  • Lectins, C-Type / genetics
  • Lectins, C-Type / metabolism
  • NADPH Oxidases / antagonists & inhibitors
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism
  • Neutrophils / immunology*
  • Phagocytosis
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Protein-Tyrosine Kinases / metabolism
  • Reactive Oxygen Species / metabolism
  • Receptors, IgG / antagonists & inhibitors
  • Receptors, IgG / genetics
  • Receptors, IgG / metabolism
  • Syk Kinase

Substances

  • FCGR1A protein, human
  • Intracellular Signaling Peptides and Proteins
  • Lectins, C-Type
  • Reactive Oxygen Species
  • Receptors, IgG
  • dectin 1
  • NADPH Oxidases
  • Protein-Tyrosine Kinases
  • SYK protein, human
  • Syk Kinase
  • Protein Kinase C