Literature DB >> 31891895

Increase in FoxP3, CD56 immune cells and decrease in glands PGRMC1 expression in the endometrium are associated with recurrent miscarriages.

Yulia Anatolievna Lyzikova1, Dmitry Aleksandrovich Zinovkin2, Md Zahidul Islam Pranjol3.   

Abstract

OBJECTIVE: Recurrent miscarriage (RM) is a multifactorial condition that involves frequent uterine anatomical abnormalities, parental karyotype abnormalities, and clotting disorders. We investigate the potential roles of endometrium FoxP3+ Tregs and CD56+ cells (uNK cells) and endometrial expression of PGRMC1 in the development of recurrent miscarriage. STUDY
DESIGN: This prospective study included 102 out of 286 cases of SA patients. The cases were divided into groups with RM (+RM) and without RM (-RM). Immunohistochemistry staining was made using primary antibodies to FoxP3, CD56, and PGRMC1 in both groups. Morphometry analyses were carried out in 10 non-overlapping high power fields. Mann-Whitney U test, Fisher two-tail test, correlation analysis and relative risk (RR) were evaluated. A p < 0.05 was considered statistically significant.
RESULTS: An increased presence of CD56-positive (p < 0.001) and FoxP3+ Treg (p = 0.0005) cells was found in the endometrium, with a reduction in PGRMC1 expression compared with -RM group (p = 0.004). A positive correlation was shown between the number of CD56-positive cells and FoxP3+ cells (r = 0.55), and an inverse correlation with PGRMC1 (r =  -0.35) in the + RM group. A similar observation was found in the -RM group, with a positive correlation of uNK cell number with the number of pregnancies (p < 0.001; r = 0.34). Endometrial infiltration of CD56-positive (p < 0.0001) and FoxP3+ (p < 0.0001) cells revealed an increased relative risk of RM. This increased risk was also revealed in SA with a loss of PGRMC1 expression (p < 0.0001).
CONCLUSION: Our prospective study suggests, for the first time, that increased endometrial infiltration of uNK, FoxP3+ Treg cells and a decreased PGRMC1 expression may play potential roles in the development of RM.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CD56; FoxP3; PGRMC1; Recurrent miscarriage; Uterine NK cells

Mesh:

Substances:

Year:  2019        PMID: 31891895     DOI: 10.1016/j.ejogrb.2019.12.019

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  6 in total

1.  Gamma-ray irradiation modulates PGRMC1 expression and the number of CD56+ and FoxP3+ cells in the tumor microenvironment of endometrial endometrioid adenocarcinoma.

Authors:  Dmitry Aleksandrovich Zinovkin; Yulia Anatolievna Lyzikova; Eldar Arkadievich Nadyrov; Daniil Rudolfovich Petrenyov; Jale Yuzugulen; Md Zahidul Islam Pranjol
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2.  Number and function of uterine natural killer cells in recurrent miscarriage and implantation failure: a systematic review and meta-analysis.

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4.  Characterisation of peri-implantation endometrial Treg and identification of an altered phenotype in recurrent pregnancy loss.

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Review 5.  What Do We Know about Classical and Non-Classical Progesterone Receptors in the Human Female Reproductive Tract? A Review.

Authors:  Yassmin Medina-Laver; Cristina Rodríguez-Varela; Stefania Salsano; Elena Labarta; Francisco Domínguez
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6.  Chemerin Effect on the Endometrial Proteome of the Domestic Pig during Implantation Obtained by LC-MS/MS Analysis.

Authors:  Kinga Orzechowska; Kamil Dobrzyń; Marta Kieżun; Agata Malinowska; Bianka Świderska; Tadeusz Kamiński; Nina Smolińska
Journal:  Cells       Date:  2022-03-30       Impact factor: 6.600

  6 in total

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