Frontiers in Immunology (Mar 2024)

Decidual γδT cells of early human pregnancy produce angiogenic and immunomodulatory proteins while also possessing cytotoxic potential

  • Jasper Nörenberg,
  • Jasper Nörenberg,
  • Jasper Nörenberg,
  • Péter Vida,
  • Isabell Bösmeier,
  • Barbara Forró,
  • Anna Nörenberg,
  • Anna Nörenberg,
  • Anna Nörenberg,
  • Ágnes Buda,
  • Diana Simon,
  • Diana Simon,
  • Szabina Erdő-Bonyár,
  • Szabina Erdő-Bonyár,
  • Pál Jáksó,
  • Kálmán Kovács,
  • Kálmán Kovács,
  • Éva Mikó,
  • Éva Mikó,
  • Éva Mikó,
  • Tímea Berki,
  • Tímea Berki,
  • Emese Mezősi,
  • Emese Mezősi,
  • Alíz Barakonyi,
  • Alíz Barakonyi,
  • Alíz Barakonyi

DOI
https://doi.org/10.3389/fimmu.2024.1382424
Journal volume & issue
Vol. 15

Abstract

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During pregnancy, the maternal immune system must allow and support the growth of the developing placenta while maintaining the integrity of the mother’s body. The trophoblast’s unique HLA signature is a key factor in this physiological process. This study focuses on decidual γδT cell populations and examines their expression of receptors that bind to non-classical HLA molecules, HLA-E and HLA-G. We demonstrate that decidual γδT cell subsets, including Vδ1, Vδ2, and double-negative (DN) Vδ1-/Vδ2- cells express HLA-specific regulatory receptors, such as NKG2C, NKG2A, ILT2, and KIR2DL4, each with varying dominance. Furthermore, decidual γδT cells produce cytokines (G-CSF, FGF2) and cytotoxic mediators (Granulysin, IFN-γ), suggesting functions in placental growth and pathogen defense. However, these processes seem to be controlled by factors other than trophoblast-derived non-classical HLA molecules. These findings indicate that decidual γδT cells have the potential to actively contribute to the maintenance of healthy human pregnancy.

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