Differential development of type 1 and type 2 cytokines and beta-chemokines in the ontogeny of healthy newborns

Biol Neonate. 1999;75(1):1-8. doi: 10.1159/000014071.

Abstract

Interleukin (IL)-2, interferon gamma (IFN-gamma; type 1 cytokines), IL-4, and IL-10 (type 2 cytokines), and beta-chemokines (MIP-1alpha and RANTES) production by cord blood lymphocytes (CBL) and peripheral blood lymphocytes (PBL) of newborns was analyzed in a cross-sectional study to examine the maturation of these components of the immune response. Immunophenotyping was performed on the same specimens. Results showed that the CD4/CD8 ratio remains stable, the percentage of natural killer cells decreases, and the number and percentage of B cells increase after birth. Analysis of cytokine production suggested that the production of all cytokines increases gradually and steadily after birth, and that IFN-gamma and IL-10 production is reduced at birth whereas IL-2 and IL-4 production is not. Finally, mitogen-stimulated beta-chemokine production was present at birth and increased slightly but significantly with age. These data indicate that a differential functional maturation of immune response after birth favoring a more precocious development of IL-2 (a type 1 cytokine) is present and should help to analyze the ontogeny of the immune system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging*
  • Cells, Cultured
  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5 / biosynthesis
  • Chemokines / biosynthesis*
  • Cross-Sectional Studies
  • Cytokines / biosynthesis*
  • Fetal Blood / cytology
  • Humans
  • Immunophenotyping
  • Infant
  • Infant, Newborn
  • Interferon-gamma / biosynthesis
  • Interleukin-10 / biosynthesis
  • Interleukin-2 / biosynthesis
  • Interleukin-4 / biosynthesis
  • Lymphocyte Count
  • Lymphocyte Subsets
  • Lymphocytes / metabolism*
  • Macrophage Inflammatory Proteins / biosynthesis

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5
  • Chemokines
  • Cytokines
  • Interleukin-2
  • Macrophage Inflammatory Proteins
  • Interleukin-10
  • Interleukin-4
  • Interferon-gamma