Age-related differentiations of Th1/Th2 cytokines in newborn infants

Efthimia Protonotariou1, Ariadne Malamitsi-Puchner, Demetrios Rizos

  • 1Hormonological Laboratory, University of Athens, Aretaieion University Hospital, Paleon Phaliro, Greece.

Insights

Newborns show distinct immune responses at birth, with high levels of interleukin-2 (IL-2) and interleukin-4 (IL-4) compared to interferon-gamma (IFN-gamma). This immune balance quickly regularizes in early neonatal life.

Area of Science:

  • Immunology
  • Neonatal Medicine
  • Pediatrics

Background:

  • The immune system undergoes significant development during the perinatal period.
  • Understanding early immune responses is crucial for neonatal health and development.

Purpose of the Study:

  • To investigate age-related immune response differentiation in newborns.
  • To measure serum concentrations of key cytokines: interleukin-2 (IL-2), interleukin-4 (IL-4), and interferon-gamma (IFN-gamma) during the perinatal period.

Main Methods:

  • Study included 57 healthy term neonates, their mothers, and 25 age-matched adult controls.
  • Cytokine concentrations were analyzed in umbilical cord (UC), first-day (1N), and fifth-day (5N) neonatal blood samples, alongside maternal serum (MS) and control serum.

Main Results:

  • IL-2 levels were high at UC, decreasing significantly by 5N.
  • IL-4 levels were elevated in neonates compared to maternal and control samples, remaining stable from UC to 5N.
  • IFN-gamma levels were lower at UC but increased significantly by 5N, with rising IFN-gamma/IL-2 and IFN-gamma/IL-4 ratios.

Conclusions:

  • Neonates exhibit a unique cytokine profile at birth, characterized by elevated IL-2 and IL-4 relative to IFN-gamma.
  • Immune system regulation appears to progress rapidly during the initial neonatal phase.
Abstract

Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Differentiation of Common Myeloid Progenitor Cells01:15

Differentiation of Common Myeloid Progenitor Cells

Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...
T Cell Types and Functions01:24

T Cell Types and Functions

When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...