IL-7/IL-7R signaling pathway might play a role in recurrent pregnancy losses by increasing inflammatory Th17 cells and decreasing Treg cells

Am J Reprod Immunol. 2016 Dec;76(6):454-464. doi: 10.1111/aji.12588. Epub 2016 Oct 21.

Abstract

Problem: We aim to investigate a possible role of IL-7/IL-7R signaling pathway in recurrent pregnancy losses (RPL).

Material and methods: Using the abortion-prone (AP) and non-abortion-prone (NP) mice model, fetal resorption rates (FRR), Th17 and Treg cells-related factors, and the effect of IL-7 and IL-7R antagonist were investigated by flow cytometry, quantitative real-time PCR, and immunohistochemistry. IL-7 and IL-7R expressions in human decidua were investigated by immunohistochemistry.

Results: In the AP mice, IL-7R antagonist treatment significantly decreased FRR by downregulating Th17 and upregulating Treg-related factors. When the NP mice were treated with IL-7, FRR was significantly increased by upregulating Th17 and downregulating Treg-related factors. In decidual stromal cells of women with RPL, increased IL-7 and decreased IL-7R expressions were present when compared to normal controls.

Conclusion: IL-7/IL-7R signaling pathway plays a possible role in RPL by upregulating Th17 immunity, meanwhile downregulating Treg immunity. Regulation of IL-7/IL-7R may be a new therapeutic strategy for RPL.

Keywords: IL-7; IL-7R; Th17 cell; Treg cell; recurrent pregnancy losses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortion, Habitual / genetics
  • Abortion, Habitual / immunology*
  • Abortion, Habitual / pathology
  • Animals
  • Case-Control Studies
  • Decidua / immunology
  • Decidua / pathology
  • Disease Models, Animal
  • Female
  • Fetal Resorption / genetics
  • Fetal Resorption / immunology*
  • Fetal Resorption / pathology
  • Gene Expression Regulation
  • Humans
  • Immunologic Factors / pharmacology
  • Interleukin-7 / genetics
  • Interleukin-7 / immunology*
  • Interleukin-7 / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred CBA
  • Mice, Inbred DBA
  • Pregnancy
  • Receptors, Interleukin-7 / antagonists & inhibitors
  • Receptors, Interleukin-7 / genetics
  • Receptors, Interleukin-7 / immunology*
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / pathology
  • Th17 Cells / immunology*
  • Th17 Cells / pathology

Substances

  • IL7 protein, human
  • Immunologic Factors
  • Interleukin-7
  • Receptors, Interleukin-7