Abstract
Problem: Placental dysfunction is present over 50% of cases of stillbirth and fetal growth 1 restriction (FGR). Villitis of unknown etiology (VUE), an inflammatory condition of the placenta characterised by maternal T cell infiltrates in the villous stroma and dysregulation
of inflammatory cytokines, is more frequent in FGR and stillbirth.
Method of Study: A novel in vitro model of placental inflammation was developed to test the hypothesis that inflammatory cells seen in VUE and/or cytokines impair placental function.
Results: Co-culture of placental explants with maternal leukocytes resulted in increased leukocytes in villous tissue and elevated concentrations of IL-1β, IL-1Ra, IL-6, IL-10 and IFN-γ (p≤0.05). Human chorionic gonadotrophin secretion was reduced following co-culture with leukocytes (p≤0.01) and cytokines (p≤0.05).
Conclusions: These observations support the hypothesis that altered placental inflammation 28 has deleterious effects on placental function. This model could be used to further 29 understanding about the pathophysiology of VUE and to test potential therapies.
of inflammatory cytokines, is more frequent in FGR and stillbirth.
Method of Study: A novel in vitro model of placental inflammation was developed to test the hypothesis that inflammatory cells seen in VUE and/or cytokines impair placental function.
Results: Co-culture of placental explants with maternal leukocytes resulted in increased leukocytes in villous tissue and elevated concentrations of IL-1β, IL-1Ra, IL-6, IL-10 and IFN-γ (p≤0.05). Human chorionic gonadotrophin secretion was reduced following co-culture with leukocytes (p≤0.01) and cytokines (p≤0.05).
Conclusions: These observations support the hypothesis that altered placental inflammation 28 has deleterious effects on placental function. This model could be used to further 29 understanding about the pathophysiology of VUE and to test potential therapies.
Original language | English |
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Journal | American journal of reproductive immunology (New York, N.Y. : 1989) |
Early online date | 6 Jul 2017 |
DOIs | |
Publication status | Published - 2017 |
Keywords
- T cells
- VUE
- inflammation
- Placental dysfunction