Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Anhui 230027, China.
Proc Natl Acad Sci U S A. 2013 Jan 15;110(3):E231-40. doi: 10.1073/pnas.1206322110. Epub 2012 Dec 27.
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.
自然杀伤 (NK) 细胞在母体-胎儿界面大量积累,但它们在成功妊娠中的确切作用仍未得到明确界定。在这里,我们提供的证据表明,在自然同种异体妊娠期间,T(H)17 细胞和局部炎症可能发生在母体-胎儿界面。我们发现,通过 CD56(bright)CD27(+)NK 亚群分泌的 IFN-γ,蜕膜 NK 细胞可抑制炎症性 T(H)17 细胞,从而促进免疫耐受和成功妊娠。在经历反复自然流产的患者中,这种 NK 细胞介导的调节反应丧失,导致 T(H)17 反应明显和广泛的局部炎症。这种局部炎症反应进一步影响 NK 细胞的调节功能,最终导致母体-胎儿耐受的丧失。因此,我们的数据通过抑制 T(H)17 介导的局部炎症,将 NK 细胞鉴定为母体-胎儿界面的关键调节细胞。