Maternal host responses to poly(I:C) during pregnancy leads to both dysfunctional immune profiles and altered behaviour in the offspring

DOI Web Site Web Site Web Site 被引用文献1件
  • Pablo Garcia‐Valtanen
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia
  • Bianca A. van Diermen
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia
  • Nerissa Lakhan
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia
  • Erin L. Lousberg
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia
  • Sarah A. Robertson
    Robinson Research Institute and Adelaide Medical School The University of Adelaide Adelaide SA Australia
  • John D. Hayball
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia
  • Kerrilyn R. Diener
    Experimental Therapeutics Laboratory School of Pharmacy and Medical Science UniSA Cancer Research Institute University of South Australia Adelaide SA Australia

説明

<jats:title>Abstract</jats:title><jats:sec><jats:title>Problem</jats:title><jats:p>Autism spectrum disorder (ASD)‐like phenotypes in murine models are linked to elevated pro‐inflammatory cytokine profiles caused by maternal immune activation (MIA), but whether MIA alters the immune response in the offspring remains unclear.</jats:p></jats:sec><jats:sec><jats:title>Method of study</jats:title><jats:p>Polyinosinic:polycytidylic acid (poly:[IC]) was used to induce MIA in immunocompetent and control TLR3‐deficient pregnant mice, and cytokine levels were measured in maternal and foetal organs. Furthermore, cytokines and behaviour responses were tested after challenge with lipopolysaccharide in 7‐day‐old and adult mice.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>MIA induced on E12 resulted in changes in the cytokine expression profile in maternal and foetal organs and correlated with TNFα and IL‐18 dysregulation in immune organs and brains from neonatal mice born to MIA‐induced dams. Such changes further correlated with altered behavioural responses in adulthood.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>MIA induced by pathogens during pregnancy can interfere with the development of the foetal immune and nervous systems leading to dysfunctional immune responses and behaviour in offspring.</jats:p></jats:sec>

収録刊行物

被引用文献 (1)*注記

もっと見る

問題の指摘

ページトップへ