[Immunoglobulin levels in premature infants on a neonatology unit]

E A Voeten1, B A Semmekrot, C M Weemaes

  • 1Subafd. Neonatologie, Academisch Ziekenhuis Nijmegen St. Radboud.

Tijdschrift Voor Kindergeneeskunde
|June 1, 1993
PubMed

Insights

Premature infants born with lower immunoglobulin G (IgG) levels face higher infection risks. Exchange transfusions and fresh frozen plasma can increase these vital antibody levels in newborns.

Area of Science:

  • Neonatal immunology
  • Pediatric infectious diseases
  • Clinical chemistry

Context:

  • Premature infants exhibit unique immunological profiles, with immunoglobulin levels varying based on gestational age and birth weight.
  • Early-life infections pose significant risks to vulnerable preterm neonates, impacting their short- and long-term health outcomes.
  • Understanding immunoglobulin dynamics is crucial for managing and preventing infections in high-risk infant populations.

Purpose:

  • To investigate the trends of serum immunoglobulin G (IgG), IgA, and IgM concentrations in premature infants during the early postpartum period.
  • To determine the correlation between gestational age, birth weight, and initial immunoglobulin levels in neonates.
  • To assess the relationship between serum IgG levels and the incidence of infections in premature infants, and evaluate the impact of therapeutic interventions on immunoglobulin concentrations.

Summary:

  • Serum IgG levels in premature infants correlate with gestational age at birth and decline postnatally, with lower levels observed in infants born between 25-29 weeks gestation compared to those born between 29-32 weeks.
  • Serum IgA remained undetectable, while IgM showed a gradual increase in premature infants during the study period.
  • Infants with initial IgG levels below 400 mg/dl had a higher incidence of infections than those with levels above 400 mg/dl. Exchange transfusions and fresh frozen plasma (FFP) increased immunoglobulin levels, unlike packed cells (PC's) or pasteurised plasma protein solution (GPO).

Impact:

  • This study highlights the critical role of early immunoglobulin G levels in predicting infection risk in premature infants.
  • Findings suggest that monitoring and potentially augmenting immunoglobulin levels could be a viable strategy for infection prevention in neonatal intensive care units.
  • The differential effects of therapeutic interventions on immunoglobulin concentrations provide valuable insights for optimizing supportive care for preterm neonates.

Related Concept Videos

Humoral Immune Responses01:36

Humoral Immune Responses

Overview
Antibody Structure01:10

Antibody Structure

Overview
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
Antibodies consist of four polypeptide chains: two identical heavy...
Transcytosis of IgG01:15

Transcytosis of IgG

Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
Immunological Memory01:23

Immunological Memory

Immunological memory, a pivotal pillar of the adaptive immune system, is responsible for the body's ability to remember and respond more swiftly and effectively to previously encountered pathogens. This remarkable feature is what makes vaccines so effective in preventing diseases.
What is Immunological Memory?
Immunological memory is an integral function of the immune system that allows it to recognize and react more rapidly and effectively to pathogens previously encountered. This feature is...
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...