Enterovirus infection during pregnancy is inversely associated with atopic disease in the offspring. Issue 12 (16th October 2018)

• Record Type: Journal Article
• Authors: Korhonen, Laura; Seiskari, Tapio; Lehtonen, Jussi; Puustinen, Leena; Surcel, Heljä‐Marja; Haapala, Anna‐Maija; Niemelä, Onni; Virtanen, Suvi M.; Honkanen, Hanna; Karjalainen, Mira; Ilonen, Jorma; Veijola, Riitta; Knip, Mikael; Lönnrot, Maria; Hyöty, Heikki
• Is Part Of: Clinical & experimental allergy. Volume 48:Issue 12(2018)
• Page Start: 1698
• Page End: 1704
• Publication Date: 2018-10-16
• Subjects: Allergy -- Periodicals; Immunology -- Periodicals; 616.97
• DOI: 10.1111/cea.13280
• Languages: English
• ISSNs: 0954-7894

Abstract

Summary: Background: Prenatal environment has been shown to influence child's risk of atopic diseases. Laboratory‐confirmed data about the role of maternal infections during pregnancy is scarce. Objective: The aim of this study was to determine the associations between serologically confirmed maternal infections during pregnancy and atopic disease in the offspring. Methods: This was a nested case‐control study within a prospective birth cohort study. Altogether 202 atopic case children and 333 matched non‐atopic control children were included. Atopic outcome was defined as having an atopic disease and IgE sensitization by the age of 5 years. We analysed serologically acute enterovirus (EV), influenza virus A (IAV) and Mycoplasma pneumoniae ( M. pneumoniae ) infections during pregnancy, and mother's seropositivity against human cytomegalovirus (CMV) and Helicobacter pylori . Results: Maternal EV infection during pregnancy was inversely associated with atopic outcome in the offspring (odds ratio 0.43; 95% confidence interval: 0.23‐0.80, P = 0.008). Acute IAV or M. pneumoniae infections or seropositivity against CMV or Helicobacter pylori were not associated with the atopic outcome. Conclusions and Clinical Relevance: Our results suggest that maternal EV infections during pregnancy are inversely associated with atopic disease in the offspring. Our finding provides further support to the previous studies suggesting an important role of the in utero environment in the development of atopic diseases.