The Role of Immune Cells in Recurrent Spontaneous Abortion

被引:113
作者
Li, Dan [1 ]
Zheng, Lianwen [1 ]
Zhao, Donghai [2 ]
Xu, Ying [1 ]
Wang, Yeling [3 ]
机构
[1] Jilin Univ, Hosp 2, Reprod Med Ctr, Changchun, Peoples R China
[2] Jilin Med Univ, Jilin, Jilin, Peoples R China
[3] Jilin Univ, Hosp 1, Dept Cardiovasc Med, Changchun 130000, Peoples R China
关键词
Recurrent spontaneous abortion; Maternal-fetal immunity; Immune cells; Immune dysfunction; REGULATORY T-CELLS; NATURAL-KILLER-CELLS; TRANSLATIONAL MINIREVIEW SERIES; HUMAN CHORIONIC-GONADOTROPIN; UMBILICAL-CORD BLOOD; PREGNANCY LOSS; SUPPRESSOR-CELLS; DENDRITIC CELLS; PERIPHERAL-BLOOD; NK CELLS;
D O I
10.1007/s43032-021-00599-y
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Recurrent spontaneous abortion affects approximately 1-2% of women of childbearing, and describes a condition in which women suffer from three or more continuous spontaneous miscarriages. However, the origin of recurrent spontaneous abortion (RSA) remains unknown, preventing effective treatment and placing stress upon patients. It has been acknowledged that successful pregnancy necessitates balanced immune responses. Therefore, immunological aberrancy may be considered a root cause of poor pregnancy outcomes. Considerable published studies have investigated the relationship between various immune cells and RSA. Here, we review current knowledge on this area, and discuss the five main categories of immune cells involved in RSA; these include innate lymphocytes (ILC), macrophages, decidual dendritic cells (DCs), and T cells. Furthermore, we sought to summarize the impact of the multiple interactions of various immune cells on the emergence of RSA. A good understanding of pregnancy-induced immunological alterations could reveal new therapeutic strategies for favorable pregnancy outcomes.
引用
收藏
页码:3303 / 3315
页数:13
相关论文
共 171 条
[11]  
[Anonymous], 2015, SCI LETT
[12]  
[Anonymous], 2020, MAR DRUGS
[13]   Progesterone during pregnancy: Endocrine-immune cross talk in mammalian species and the role of stress [J].
Arck, Petra ;
Hansen, Peter J. ;
Jericevic, Biserka Mulac ;
Piccinni, Marie-Pierre ;
Szekeres-Bartho, Julia .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2007, 58 (03) :268-279
[14]   Nuclear Receptors of the Peroxisome Proliferator-Activated Receptor (PPAR) Family in Gestational Diabetes: From Animal Models to Clinical Trials [J].
Arck, Petra ;
Toth, Bettina ;
Pestka, Aurelia ;
Jeschke, Udo .
BIOLOGY OF REPRODUCTION, 2010, 83 (02) :168-176
[15]   A physiological role for inducible FOXP3+ TREG cells Lessons from women with reproductive failure [J].
Arruvito, Lourdes ;
Sotelo, Ana I. ;
Billordo, Ariel ;
Fainboim, Leonardo .
CLINICAL IMMUNOLOGY, 2010, 136 (03) :432-441
[16]   The biology of innate lymphoid cells [J].
Artis, David ;
Spits, Hergen .
NATURE, 2015, 517 (7534) :293-301
[17]   Differential regulation and function of the Fas/Fas ligand system in human trophoblast cells [J].
Aschkenazi, S ;
Straszewski, S ;
Verwer, KMA ;
Foellmer, H ;
Rutherford, T ;
Mor, G .
BIOLOGY OF REPRODUCTION, 2002, 66 (06) :1853-1861
[18]   ESHRE guideline: recurrent pregnancy loss [J].
Atik, Ruth Bender ;
Christiansen, Ole Bjarne ;
Elson, Janine ;
Kolte, Astrid Marie ;
Lewis, Sheena ;
Middeldorp, Saskia ;
Nelen, Willianne ;
Peramo, Braulio ;
Quenby, Siobhan ;
Vermeulen, Nathalie ;
Goddijn, Mariette .
HUMAN REPRODUCTION OPEN, 2018, 2018 (02)
[19]   Recurrent pregnancy loss: the key potential mechanisms [J].
Baek, Kwang-Hyun ;
Lee, Eung-Ji ;
Kim, Yong-Soo .
TRENDS IN MOLECULAR MEDICINE, 2007, 13 (07) :310-317
[20]   Histone deacetylases in cardiovascular and metabolic diseases [J].
Bagchi, Rushita A. ;
Weeks, Kate L. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2019, 130 :151-159