Fetal-maternal interactions during pregnancy: a 'three-in-one' perspective

Front Immunol. 2023 Jun 7:14:1198430. doi: 10.3389/fimmu.2023.1198430. eCollection 2023.

Abstract

A successful human pregnancy requires the maternal immune system to recognize and tolerate the semi-allogeneic fetus, allowing for appropriate trophoblasts invasion and protecting the fetus from invading pathogens. Therefore, maternal immunity is critical for the establishment and maintenance of pregnancy, especially at the maternal-fetal interface. Anatomically, the maternal-fetal interface has both maternally- and fetally- derived cells, including fetal originated trophoblasts and maternal derived immune cells and stromal cells. Besides, a commensal microbiota in the uterus was supposed to aid the unique immunity in pregnancy. The appropriate crosstalk between fetal derived and maternal originated cells and uterine microbiota are critical for normal pregnancy. Dysfunctional maternal-fetal interactions might be associated with the development of pregnancy complications. This review elaborates the latest knowledge on the interactions between trophoblasts and decidual immune cells, highlighting their critical roles in maternal-fetal tolerance and pregnancy development. We also characterize the role of commensal bacteria in promoting pregnancy progression. Furthermore, this review may provide new thought on future basic research and the development of clinical applications for pregnancy complications.

Keywords: NK; Treg; commensal microbiota; interactions; macrophage; trophoblast.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Decidua*
  • Female
  • Fetus
  • Humans
  • Pregnancy
  • Pregnancy Complications*
  • Trophoblasts
  • Uterus

Grants and funding

This study was supported by the National Nature Science Foundation of China (No. 82001637), Natural Science Foundation of Jiangsu Province (No. BK20200130) and Medical Science and Technology project of Henan Province (LHGJ20210468).