Natural killer cells promote immune tolerance by regulating inflammatory TH17 cells at the human maternal-fetal interface Academic Article uri icon

Overview

MeSH Major

  • Immune Tolerance
  • Killer Cells, Natural
  • Maternal-Fetal Exchange
  • Th17 Cells

abstract

  • Natural killer (NK) cells accumulate at the maternal-fetal interface in large numbers, but their exact roles in successful pregnancy remain poorly defined. Here, we provide evidence that T(H)17 cells and local inflammation can occur at the maternal-fetal interface during natural allogenic pregnancies. We found that decidual NK cells promote immune tolerance and successful pregnancy by dampening inflammatory T(H)17 cells via IFN-γ secreted by the CD56(bright)CD27(+) NK subset. This NK-cell-mediated regulatory response is lost in patients who experience recurrent spontaneous abortions, which results in a prominent T(H)17 response and extensive local inflammation. This local inflammatory response further affects the regulatory function of NK cells, leading to the eventual loss of maternal-fetal tolerance. Thus, our data identify NK cells as key regulatory cells at the maternal-fetal interface by suppressing T(H)17-mediated local inflammation.

publication date

  • January 15, 2013

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3549088

Digital Object Identifier (DOI)

  • 10.1073/pnas.1206322110

PubMed ID

  • 23271808

Additional Document Info

start page

  • E231

end page

  • 40

volume

  • 110

number

  • 3