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Updated: Mar 22, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Cellular gene expression induced by parasite antigens and allergens in neonates from parasite-infected mothers
Peter T Soboslay1, Thorsten Orlikowsky2, Xiangsheng Huang1
1Institute for Tropical Medicine, University of Tübingen (UKT), Wilhelmstr. 27, 72074 Tübingen, Germany.
Insights
Prenatal exposure to parasite antigens can alter newborn immune responses. Lack of prenatal exposure may predispose neonates to immune, blood, and skin disorders later in life.
Area of Science:
- Immunology
- Developmental Biology
- Genetics
Background:
- Prenatal exposure to parasite antigens or allergens can shape postnatal immune responses, potentially leading to tolerance and increased susceptibility to infections or sensitization to allergens.
- In utero exposure to parasite antigens distinctly alters cellular gene expression in newborns, influencing their immune system development.
Purpose of the Study:
- To investigate the impact of prenatal parasite antigen exposure on gene expression profiles in umbilical cord blood cells (UCBC).
- To compare gene expression differences between neonates exposed (Para-POS) and unexposed (Para-NEG) to parasite antigens in utero.
Main Methods:
- Gene microarrays were used to analyze gene expression in UCBC from Para-POS and Para-NEG neonates.
- UCBC were activated with helminth (Onchocerca volvulus), amoeba (Entamoeba histolytica), or mite (Dermatophagoides farinae) antigens.
Main Results:
- Significant differences in gene expression were observed between Para-POS and Para-NEG groups when UCBC were stimulated with helminth antigens or allergens.
- Genes involved in immune regulation, inflammation, and apoptosis showed altered expression patterns.
- Para-NEG neonates exhibited enhanced expression of innate immune response genes, while Para-POS neonates showed reduced expression of MHC class II and STAT genes.
- Functional gene network analysis revealed higher expression values in Para-NEG neonates for cellular growth, proliferation, and immune responses.
Conclusions:
- Prenatal parasite exposure can sensitize the immune system without inducing aberrant inflammatory responses.
- Neonates lacking prenatal parasite antigen encounter may have gene expression profiles predisposing them to immunological, hematological, and dermatological disorders upon postnatal exposure.
- Gene expression profiles in UCBC reflect prenatal immune programming and potential susceptibility to postnatal immune-related conditions.
Abstract:
Prenatal exposure to parasite antigens or allergens will influence the profile and strength of postnatal immune responses, such contact may tolerize and increase susceptibility to future infections or sensitize to environmental allergens. Exposure in utero to parasite antigens will distinctly alter cellular gene expression in newborns. Gene microarrays were applied to study gene expression in umbilical cord blood cell (UCBC) from parasite-exposed (Para-POS) and non-exposed (Para-NEG) neonates. UCBC were activated with antigens of helminth (Onchocerca volvulus), amoeba (Entamoeba histolytica) or allergens of mite (Dermatophagoides farinae). When UCBC from Para-POS and Para-NEG newborns were exposed to helminth antigens or allergens consistent differences occurred in the expression of genes encoding for MHC class I and II alleles, signal transducers of activation and transcription (STATs), cytokines, chemokines, immunoglobulin heavy and light chains, and molecules associated with immune regulation (SOCS, TLR, TGF), inflammation (TNF, CCR) and apoptosis (CASP). Expression of genes associated with innate immune responses were enhanced in Para-NEG, while in Para-POS, the expression of MHC class II and STAT genes was reduced. Within functional gene networks for cellular growth, proliferation and immune responses, Para-NEG neonates presented with significantly higher expression values than Para-POS. In Para-NEG newborns, the gene cluster and pathway analyses suggested that gene expression profiles may predispose for the development of immunological, hematological and dermatological disorders upon postnatal helminth parasite infection or allergen exposure. Thus, prenatal parasite contact will sensitize without generating aberrant inflammatory immune responses, and increased pro-inflammatory but decreased regulatory gene expression profiles will be present in those neonates lacking prenatal parasite antigen encounter.
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