Short-term cytolytic mediators' expression in decidual lymphocytes is enhanced by interleukin-15

Natasa Strbo1, Gordana Laskarin, Tatjana Bogovic Crncic

  • 1Department of Physiology and Immunology, Medical Faculty, University of Rijeka, Rijeka, Croatia.

Insights

Interleukin-15 (IL-15) and decidual adherent cells (DAC) enhance the killing ability of first-trimester decidual lymphocytes (DL). IL-15, likely from DAC, boosts cytotoxic mediators and cell-killing potential, similar to IL-2.

Area of Science:

  • Immunology
  • Reproductive Biology
  • Cell Biology

Background:

  • Decidual lymphocytes (DL) play a crucial role in early pregnancy.
  • The cytolytic potential of DL is critical for immune regulation during gestation.
  • Decidual adherent cells (DAC) are a unique cell population in the decidua.

Purpose of the Study:

  • To investigate the comparative effects of Interleukin-15 (IL-15) and Interleukin-2 (IL-2) on the cytolytic potential of first-trimester decidual lymphocytes (DL).
  • To determine the role of decidual adherent cells (DAC) in modulating DL cytotoxicity.
  • To explore the interplay between DAC, IL-15, and DL effector functions.

Main Methods:

  • Decidual mononuclear cells were isolated and cultured with IL-15, IL-2, DAC, or anti-IL-15 antibody.
  • Expression of cytotoxic mediators (perforin, FasL, granzyme B) was assessed at the mRNA level.
  • Cytolytic activity of DL was measured using PKH-26 cytotoxicity assays against target cells (K-562, P815).

Main Results:

  • IL-15 enhanced the transcription of perforin, FasL, and granzyme B in DL.
  • DAC sustained perforin expression in DL, an effect abrogated by anti-IL-15 antibody.
  • DAC significantly increased DL cytotoxicity against K-562 cells, mediated by IL-15.

Conclusions:

  • IL-15, likely produced by DAC, upregulates cytotoxic mediators and enhances the perforin-mediated cytotoxicity of DL.
  • The effect of IL-15 on DL cytotoxicity is comparable to that of high concentrations of IL-2.
  • DAC play a significant role in regulating the immune function of decidual lymphocytes during early pregnancy.
Abstract