| Literature DB >> 28271497 |
Kathrin Klar1, Sophie Perchermeier1, Sonakshi Bhattacharjee1, Hani Harb2, Thure Adler3, Rouzanna Istvanffy4, Eva Loffredo-Verde1, Robert A Oostendorp4, Harald Renz2, Clarissa Prazeres da Costa1.
Abstract
Schistosomiasis is a nontransplacental helminth infection. Chronic infection during pregnancy suppresses allergic airway responses in offspring. We addressed the question whether in utero exposure to chronic schistosome infection (Reg phase) in mice affects B-cell and T-cell development. Therefore, we focused our analyses on T-cell differentiation capacity induced by epigenetic changes in promoter regions of signature cytokines in offspring. Here, we show that naïve T cells from offspring of schistosome infected female mice had a strong capacity to differentiate into TH 1 cells, whereas TH 2 differentiation was impaired. In accordance, reduced levels of histone acetylation of the IL-4 promoter regions were observed in naïve T cells. To conclude, our mouse model revealed distinct epigenetic changes within the naïve T-cell compartment affecting TH 2 and TH 1 cell differentiation in offspring of mothers with chronic helminth infection. These findings could eventually help understand how helminths alter T-cell driven immune responses induced by allergens, bacterial or viral infections, as well as vaccines.Entities:
Keywords: Epigenetic histone modification; In utero programming; Maternal helminth infection; Schistosomiasis; T-cell differentiation
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Year: 2017 PMID: 28271497 DOI: 10.1002/eji.201646836
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532