Lymphocytes in Placental Tissues: Immune Regulation and Translational Possibilities for Immunotherapy.
Tom ErkersArwen StikvoortMichael UhlinPublished in: Stem cells international (2017)
Immune modulation at the fetomaternal interface is crucial to ensure that the fetal allograft is not rejected. In the present review, the focus is to describe basic functions of lymphocyte populations and how they may contribute to fetomaternal immune regulation, as well as determining what proportions and effector functions of these cells are reported to be present in placental tissues in humans. Also explored is the possibility that unique cell populations at the fetomaternal interface may be targets for adoptive cell therapy. Increasing the understanding of immune modulation during pregnancy can give valuable insight into other established fields such as allogeneic hematopoietic stem cell transplantation and solid organ transplantation. In these settings, lymphocytes are key components that contribute to inflammation and rejection of either patient or donor tissues following transplantation. In contrast, an allogeneic fetus eludes rejection by the maternal immune system.
Keyphrases
- cell therapy
- allogeneic hematopoietic stem cell transplantation
- stem cells
- gene expression
- mesenchymal stem cells
- peripheral blood
- induced apoptosis
- acute lymphoblastic leukemia
- stem cell transplantation
- dendritic cells
- case report
- signaling pathway
- single cell
- immune response
- cell proliferation
- pregnant women
- endoplasmic reticulum stress
- birth weight
- contrast enhanced
- pregnancy outcomes
- kidney transplantation