Problem: The maternal-fetal immune abnormalities can result in recurrent spontaneous abortion (RSA). The role of NKG2C and LILRB1 pNK subsets in predicting pregnancy loss is uncertain.
Method Of Study: In this study, we aimed to compare the percentage of CD3 CD56 NK cells, NKG2C NK cells, and LILRB1 NK cells in peripheral blood between healthy pregnant women (HC group), RSA women followed by normal pregnancy (RSA-N group) and RSA women followed by abortion (RSA-A group) in the first trimester via flow cytometry, and explore the prediction value of NKG2C and LILRB1 NK cells for pregnancy loss in RSA via ROC curve. The MFI of NKG2C and LILRB1 of dNK were compared between and HC and RSA-A groups.
Results: The percentage of CD3-CD56 pNK cells between HC, RSA-N, and RSA-A groups shows no significant difference. In peripheral blood, the percentage of NKG2C NK cells were significantly increased in the RSA-A group than HC group and RSA-N group, and the percentage of LILRB1 NK cell were significantly decreased in the RSA-A group. The MFI of NKG2C and LILRB1 of dNK showed a similar trend with peripheral blood between HC and RSA-A groups. The NKG2C and LILRB1 NK cells were an independent risk factor for predicting pregnancy loss in RSA patients, with an area under the ROC curves (AUC) of .77 and .71 respectively.
Conclusion: Women with recurrent spontaneous abortion have abnormal NKG2C and LILRB1 pNK subsets, which could reflect immune abnormalities at the maternal-fetal interface, and NKG2C and LILRB1 pNK subsets could be a good indicator for the prediction of pregnancy loss.
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http://dx.doi.org/10.1111/aji.13627 | DOI Listing |
Am J Reprod Immunol
June 2023
Department of Obstetrics and Gynecology, Shengjing Hospital, China Medical University, Shenyang, China.
Problem: The maternal-fetal immune abnormalities can result in recurrent spontaneous abortion (RSA). The role of NKG2C and LILRB1 pNK subsets in predicting pregnancy loss is uncertain.
Method Of Study: In this study, we aimed to compare the percentage of CD3 CD56 NK cells, NKG2C NK cells, and LILRB1 NK cells in peripheral blood between healthy pregnant women (HC group), RSA women followed by normal pregnancy (RSA-N group) and RSA women followed by abortion (RSA-A group) in the first trimester via flow cytometry, and explore the prediction value of NKG2C and LILRB1 NK cells for pregnancy loss in RSA via ROC curve.
Am J Reprod Immunol
November 2022
Department of Transplantation Immunology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Problem: NK cells are important for healthy pregnancy and aberrant phenotypes or effector functions have been associated with RPL. We compared expression of a broad panel of NK cell receptors, including immune checkpoint receptors, and investigated their clinical association with RPL as this might improve patient stratification and prediction of RPL.
Method Of Study: Peripheral blood mononuclear cells were isolated from 52 women with RPL and from 2 women with an uncomplicated pregnancy for flowcytometric analysis and plasma was used to determine anti-CMV IgG antibodies.
Front Immunol
July 2022
Placenta Lab, Department of Obstetrics, Jena University Hospital, Jena, Germany.
Members of the innate immune system, innate lymphoid cells (ILCs), encompass five major populations (Natural Killer (NK) cells, ILC1s, ILC2s, ILC3s, and lymphoid tissue inducer cells) whose functions include defense against pathogens, surveillance of tumorigenesis, and regulation of tissue homeostasis and remodeling. ILCs are present in the uterine environment of humans and mice and are dynamically regulated during the reproductive cycle and pregnancy. These cells have been repurposed to support pregnancy promoting maternal immune tolerance and placental development.
View Article and Find Full Text PDFFront Cell Infect Microbiol
April 2022
Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA, United States.
AIDS
May 2020
Division of Infection Diseases and Geographic Medicine, Department of Medicine.
Objective: Our objective was to investigate the mechanisms that govern natural killer (NK)-cell responses to HIV, with a focus on specific receptor--ligand interactions involved in HIV recognition by NK cells.
Design And Methods: We first performed a mass cytometry-based screen of NK-cell receptor expression patterns in healthy controls and HIV individuals. We then focused mechanistic studies on the expression and function of T cell immunoreceptor with Ig and ITIM domains (TIGIT).
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