CD14 polymorphisms in mother and infant, soluble CD14 in breast milk and atopy development in the infant (KOALA

Bianca E P Snijders1, Foekje F Stelma, Naomi E Reijmerink

  • 1Department of Epidemiology, Care and Public Health Research Institute, Maastricht University, Maastricht, The Netherlands. bep.snijders@epid.unimaas.nl

Insights

The CD14/-1619 gene variant in infants is linked to a reduced risk of eczema. Breast milk soluble CD14 (sCD14) levels did not alter this association in children up to age two.

Area of Science:

  • Immunogenetics
  • Pediatric Allergy
  • Molecular Epidemiology

Background:

  • CD14 gene polymorphisms are implicated in infant atopic conditions.
  • Maternal CD14 genotypes influence soluble CD14 (sCD14) levels in breast milk.
  • The combined impact of infant/maternal CD14 genotypes and breast milk sCD14 on atopy requires further investigation.

Purpose of the Study:

  • To examine the association between CD14 single nucleotide polymorphisms (SNPs), breast milk sCD14 levels, and atopy development up to age two.
  • To determine if breast milk sCD14 modifies the effect of infant CD14 genotype on atopy.
  • To assess the relationship between maternal CD14 SNPs and breast milk sCD14 levels.

Main Methods:

  • Investigated four CD14 SNPs in 698 infants and 188 mothers.
  • Analyzed associations using logistic and linear regression models.
  • Examined interactions between infant CD14 genotype, breast milk sCD14, and atopy development.

Main Results:

  • The CD14/-1619 SNP showed a significant association with eczema development.
  • CC homozygotes for CD14/-1619 had a reduced risk of eczema compared to TT homozygotes (aOR=0.56).
  • No significant interaction was found between infant CD14 genotype and breast milk sCD14 levels on atopy; maternal SNPs did not correlate with breast milk sCD14.

Conclusions:

  • Infant CD14/-1619 CC genotype is associated with a lower risk of eczema.
  • Breast milk sCD14 levels do not appear to modify the relationship between infant CD14 genotype and atopy development.
  • The study did not find evidence supporting a modifying role of breast milk sCD14 in the context of infant CD14 genotype and atopy up to age two.

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...
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
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...