Maternal immunization downregulates offspring TCD4 regulatory cells (Tregs) thymic maturation without implications for allergy inhibition

Scand J Immunol. 2018 Dec;88(6):e12721. doi: 10.1111/sji.12721. Epub 2018 Oct 28.

Abstract

The regulation of offspring allergy development mediated by maternal immunization was evidenced by several groups, and this mechanism seems to involve the induction of regulatory T cells (Tregs) on offspring. Here, we aimed to evaluate whether the effect of maternal immunization on offspring Tregs occurs as a result of peripheral or central modulation. Briefly, C57BL/6 female mice were immunized with OVA in Alum or Alum alone and boosted with OVA in saline or saline only after 10 and 20 days. Non-immunized offspring serum, thymus and spleen were evaluated at 3 or 20 days old, and some groups of pups were submitted to neonatal OVA-immunization protocol for the subsequent evaluation of antibody production and allergic response. Our experimental protocol could be validated because maternal OVA-immunization inhibited offspring allergic response as evidenced by the suppression of offspring IgE production and allergic lung inflammation. Interestingly, maternal immunization reduced the frequency of offspring thymic Tregs with an opposite effect on spleen Tregs. Furthermore, after neonatal immunization, the frequency of lung-infiltrated Tregs was also augmented on offspring from immunized mothers. In conclusion, maternal OVA-immunization can inhibit the thymic maturation of offspring Tregs without implications on peripheral Tregs induction and allergy inhibition.

Keywords: Treg cells; allergy; maternal immunization; thymus.

MeSH terms

  • Animals
  • Animals, Newborn
  • Antibody Formation
  • Disease Models, Animal
  • Female
  • Hypersensitivity / immunology*
  • Immune Tolerance
  • Immunization
  • Immunoglobulin E / metabolism
  • Maternal Exposure / adverse effects
  • Maternal-Fetal Exchange
  • Mice
  • Mice, Inbred C57BL
  • Pneumonia / immunology*
  • Pregnancy
  • Spleen / immunology*
  • T-Lymphocytes, Regulatory / immunology*
  • Thymus Gland / immunology*

Substances

  • Immunoglobulin E