z-logo
Premium
Recurrent miscarriage is associated with a decline of decidual natural killer cells expressing killer cell immunoglobulin‐like receptors specific for human leukocyte antigen C
Author(s) -
Wang Shan,
Li YanPing,
Ding Bo,
Zhao YueRan,
Chen ZiJiang,
Xu ChengYan,
Fu YiBing,
Wang XieTong
Publication year - 2014
Publication title -
journal of obstetrics and gynaecology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 50
eISSN - 1447-0756
pISSN - 1341-8076
DOI - 10.1111/jog.12329
Subject(s) - immunology , natural killer cell , receptor , andrology , miscarriage , decidua , antibody , medicine , biology , pregnancy , fetus , cytotoxic t cell , in vitro , biochemistry , genetics , placenta
Aim To investigate the relationship between natural killer ( NK ) cell phenotype and recurrent miscarriage ( RM ). Methods We studied killer cell immunoglobulin‐like receptor ( KIR ) expression on decidual NK cells in women with RM . Results The expression of KIR2DL1/S1 on CD 56 + CD 16 − NK cells in the deciduas of these women was significantly lower than in that of control subjects ( P  = 0.026). There was a significant decline in the frequency of CD 56 + CD 16 − NK cells staining for KIR2DL1/S1 and KIR2DL2/S2/L3 throughout the first trimester in patients ( P  < 0.05). Furthermore, by stratification of the women in three groups according to gestational stage, it was found that KIR2DL1/S1 expressing NK cells were significantly decreased in all groups, especially around gestational days 50–70 ( P  = 0.010). Conclusion This is the first report to demonstrate that RM is associated with a decline in the frequency of decidual NK cells expressing KIR specific for human leukocyte antigen ( HLA )‐ C , and in which gestational stage was considered. The results suggest that KIR phenotype contributes to the pathogenesis of the disease, and that assessment of KIR may serve as a diagnostic tool.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom