Progress in reproductive immunity research

Progress in reproductive immunity research

Progress in reproductive immunity research

December 26, 2017 Source: University of Science and Technology of China

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A special maternal-fetal interface needs to be formed during embryonic development to protect the normal development of the fetus. The maternal-fetal interface includes a large number of decidual natural killer cells (dNK), which account for 70% of the total lymphocytes in the first trimester of pregnancy. It is unclear what role such a large number of dNK cells play in embryonic development. Recently, Wei Haiming and Tian Zhigang, professors of the Institute of Immunology, University of Science and Technology of China, found that a large number of CD49a+Eomes+NK subpopulations existed in the decidua tissue of human and mouse early pregnancy, and promoted embryo development by secreting growth factors. Loss of this NK cell that secretes growth factors can cause embryo growth restriction. On December 19th, relevant research results were published on Immunity.

Embryonic developmental restriction and repeated abortion are common pregnancy-related diseases, which are closely related to the abnormal microenvironment of the maternal and fetal immune system. Through the whole-genome screening, the research team compared the functional genes of NK cells and peripheral blood NK cells, and found that early pregnancy decidual NK cells highly expressed PTN, OGN and other growth factors important for early embryo development. HLA-G expressed by embryonic-derived extravillous trophoblast cells interacts with decidual NK cells to induce NK cells to express growth factors in large amounts and promote embryo development. In patients with repeated abortion, the ability of decidual NK cells to express growth factors was found to be significantly reduced, which could not support the normal development of early embryos.

In the study of the mouse pregnancy model, it was found that the Nfil3 transcription factor is important for safeguarding the function of the CD49a+Eomes+ NK cell subset. In the absence of this transcription factor, the NK cells in the maternal-fetal interface of the mouse are greatly reduced, and intrauterine embryos are severely restricted in growth. In addition, the study found that the incidence of abortion and embryo growth restriction in older age is higher. Using the old mouse model to study the mechanism, it is found that although the number of NK cells in aged rats is not much changed, the ability to secrete growth factors is significant. reduce.

In order to save the embryo growth restriction caused by the decrease of NK cell secretion growth factor, the research group induced decidual-like NK cells with bone marrow hematopoietic stem cells in vitro, and the mice were treated with intravenous transfer, and the aged rats after transfer were The growth outcome of the growth factor-deficient mice was significantly improved and the embryo growth restriction was relieved. The study found that NK cells have unique physiological functions to promote embryonic development in the decidual tissue. The directional induction of specific function NK cell adoptive transfer program has provided a clinical treatment for embryo growth restriction and recurrent miscarriage. New ideas.

The research work was funded by the National Natural Science Foundation.

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