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Relation between stressful life events, neuropeptides and cytokines: results from the LISA birth cohort study
Gunda Herberth1, Annegret Weber, Stefan Röder
1Department of Environmental Immunology, Helmholtz Centre for Environmental Research-UFZ Leipzig, Leipzig, Germany. gunda.herberth@ufz.de
Insights
Parental divorce in children is linked to higher vasoactive intestinal peptide (VIP) and interleukin-4 (IL-4) levels, suggesting VIP may mediate stress effects on immune responses. Parental unemployment impacts immune regulation via unknown mechanisms.
Area of Science:
- Immunology
- Psychoneuroimmunology
- Pediatric Allergy
Background:
- Stressful life events are known to influence allergic disease development.
- The precise mechanisms linking psychological stress to immune system dysfunction remain unclear.
- Understanding these links is crucial for pediatric health and allergy prevention.
Purpose of the Study:
- To investigate the association between stressful life events and neuropeptide/cytokine concentrations in children.
- To explore potential mediators of stress-induced immune changes in pediatric populations.
- To identify specific life stressors that correlate with immune markers in children.
Main Methods:
- Analysis of blood samples from 234 six-year-old children participating in the LISAplus study.
- Measurement of neuropeptides: vasoactive intestinal peptide (VIP), somatostatin (SOM), substance P (SP).
- Quantification of Th1/Th2 cytokines: interferon-gamma (IFN-gamma) and interleukin-4 (IL-4).
- Assessment of parental-reported life events (e.g., parental separation, unemployment, family illness/death) via questionnaire.
Main Results:
- Children of separated/divorced parents exhibited elevated VIP and IL-4 levels.
- Parental unemployment was associated with reduced IFN-gamma concentrations.
- Severe family illness/death showed no significant association with measured neuropeptides or cytokines.
- Concomitant severe family illness and death correlated with decreased SP levels.
Conclusions:
- Vasoactive intestinal peptide (VIP) may act as a mediator between parental separation and a Th2-shifted immune response in children.
- Parental unemployment affects children's immune regulation through an unidentified pathway.
- Reduced substance P (SP) levels in children experiencing family bereavement did not appear to impact immune regulation significantly.
Abstract:
Stressful life events evidently have an impact on development of allergic diseases, but the mechanism linking stress to pathological changes of immune system function is still not fully understood. The aim of our study was to investigate the relationship between stressful life events, neuropeptide and cytokine concentrations in children. Within the LISAplus (Life style-Immune system-Allergy) study, blood samples from children of 6 yr of age were analysed for concentration of the neuropeptides vasoactive intestinal peptide (VIP), somatostatin (SOM), substance P (SP) and the Th1/Th2 cytokines interferon-gamma (IFN-gamma) and interleukin (IL)-4. Life events such as severe disease or death of a family member, unemployment or divorce of the parents were assessed with a questionnaire filled in by the parents. For 234 children, blood analysis and questionnaire data regarding life events were available. Children with separated/divorced parents showed high VIP levels and high concentrations of the Th2 cytokine IL-4 in their blood. Severe diseases and death of a family member were neither associated with neuropeptide levels nor with cytokine concentrations. Unemployment of the parents was associated with decreased IFN-gamma concentrations in children's blood but not with neuropeptide levels, whereas children experiencing concomitant severe disease and death of a family member had reduced SP blood levels. The neuropeptide VIP might be a mediator between stressful life events and immune regulation contributing to the Th2 shifted immune response in children with separated/divorced parents. Unemployment of the parents was associated with immune regulation in children on the basis of a still unknown mechanism whereas reduced SP levels seem to have no effect on immune regulation.
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