Distinct abnormalities in the innate immune system of children with Down syndrome

J Pediatr. 2010 May;156(5):804-9, 809.e1-809.e5. doi: 10.1016/j.jpeds.2009.12.006. Epub 2010 Feb 20.

Abstract

Objective: To analyze the frequency and phenotype of cells of the innate immune system in the peripheral blood of children with Down syndrome (DS).

Study design: Flow cytometric analysis of expression of cell surface markers was performed in children with DS (n = 41) and healthy age-matched controls (n = 41).

Results: Compared with controls, children with DS had significantly lower absolute total leukocyte counts, lymphocytes, monocytes, and granulocytes, but 1.5-times higher absolute numbers of CD14(dim)CD16(+) monocytes (147 x 10(6)/L vs 93 x 10(6)/L; P = .02). This difference is fully explained by a higher percentage of CD14(dim)CD16(+) monocytes within the monocyte compartment (28.7% vs 13.4%; P <.001). The absolute numbers of myeloid dendritic cells were lower in DS (13.8 x 10(6)/L vs 22.7 x 10(6)/L; P <.001). The numbers of plasmacytoid dendritic cells and natural killer cells were normal. Absolute numbers of invariant natural killer T cells were very low overall, but significantly lower in children with DS than in controls (1.2 x 10(6)/L vs 3.7 x 10(6)/L; P = .01).

Conclusions: Children with DS exhibited distinct abnormalities in cells of the innate immune system. Most strikingly, they had a high number of proinflammatory CD14(dim)CD16(+) monocytes. This elevated level of CD14(dim)CD16(+) monocytes may play an important role in the onset and maintenance of chronic inflammatory disease in DS.

MeSH terms

  • Adaptive Immunity / immunology
  • Antigens, CD / analysis
  • Child
  • Child, Preschool
  • Dendritic Cells / cytology
  • Down Syndrome / immunology*
  • Female
  • Humans
  • Immunity, Innate / immunology*
  • Immunophenotyping
  • Infant
  • Killer Cells, Natural / cytology*
  • Leukocyte Count
  • Lipopolysaccharide Receptors / analysis
  • Male
  • Monocytes / immunology
  • Receptors, IgG / analysis

Substances

  • Antigens, CD
  • Lipopolysaccharide Receptors
  • Receptors, IgG