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Published on: August 12, 2020
Development and maturation of the immune system in preterm neonates: results from a whole genome expression study
Magdalena Zasada1, Przemko Kwinta1, Wojciech Durlak2
1Department of Pediatrics, Polish-American Children's Hospital, Faculty of Medicine, Jagiellonian University, Wielicka 265, 30-663 Krakow, Poland.
Insights
This study tracked gene expression in preterm infants, revealing immune system development pathways are significantly influenced by post-birth environment and gestational age. Gene expression patterns stabilize with similar postconceptional age.
Area of Science:
- Neonatal Immunology
- Developmental Biology
- Genomics
Background:
- Immune system development in preterm neonates is complex and influenced by various factors.
- Understanding gene expression changes post-birth is crucial for preterm infant care.
Purpose of the Study:
- To investigate the sequential gene expression related to immune system development in preterm neonates.
- To determine the impact of the postnatal environment on gene expression patterns.
- To identify gestational age-dependent gene expression trends.
Main Methods:
- Prospective study of three preterm infant cohorts (extremely, very, moderately preterm).
- Blood samples collected on day 5 and day 28 of life.
- Gene expression analysis using GeneChip Human Gene 1.0ST microarrays.
Main Results:
- Identified subsets of genes with monotone expression trends on days 5 and 28.
- Pathway enrichment analysis highlighted host immunity pathways, including T-cell receptor signaling and IgA production.
- Significant differential gene expression (4431 genes) observed between day 5 and day 28.
- Gene expression similarity was noted in preterm infants with the same postconceptional age, irrespective of initial gestational age differences.
Conclusions:
- Postnatal environmental factors significantly influence immune system gene expression in preterm infants.
- Gestational age is a key determinant of specific immune pathways.
- Postconceptional age is a strong predictor of similar gene expression profiles in preterm neonates.
Abstract:
To expand the knowledge about the consecutive expression of genes involved in the immune system development in preterm neonates and to verify if the environment changes the gene expression after birth we conducted a prospective study that included three cohorts: (A) extremely (gestational age (GA): 23-26 weeks; n = 41), (B) very (GA: 27-29 weeks; n = 39), and (C) moderately preterm infants (GA: 30-32 weeks; n = 33). Blood samples were drawn from the study participants on the 5th and 28th day of life (DOL). The mRNA samples were evaluated for gene expression with the use of GeneChip Human Gene 1.0ST microarrays. Differential expression analysis revealed small subsets of genes that presented positive or negative monotone trends in both the 5th (138 genes) and 28th DOL (308 genes) in the three subgroups of patients. Based on pathway enrichment analysis, we found that most of the pathways that revealed a positive monotone trend were involved in host immunity. The most significantly GA dependent pathways were T-cell receptor signaling pathway and intestinal immune network for IgA production. Overall 4431 genes were differentially expressed between the 5th and 28th DOL. Despite differences in gestational age, patients with the same postconceptional age have a very similar expression of genes.
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