Literature DB >> 16134529

[Expression of T-lymphocytes and cytokines in the decidua of mifepristone with misoprostol for terminating early pregnancy].

S Lu1, R Wu, Z Wang.   

Abstract

OBJECTIVE: To investigate the expression of T-lymphocyte subsets (CD3+, CD4+, CD8+), natural killer cells (NK cells, CD56+, CD16+), tumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta (TGF-beta) in mifepristone and misoprostod treated ducidua for terminating human early pregnancy.
METHODS: Thirty eight women who volunteered to terminate their pregnancy were divided into 3 groups: mifepristone group (group I, n = 13), mifepristone with misoprostol group (group II, n = 12) and control group (group Il, n = 13), The expression of T-lymphocyte subsets, NK cells, TNF-alpha and TGF-beta were assessed by flow cytometry.
RESULTS: The expression of CD4+ were (30.91 +/- 2.57)% and (31.58 +/- 3.28)% in group I and II respectively. Which were significantly higher than that in group III (25.64 +/- 2.36)% (P < 0.05, P < 0.01). CD56+ were (22.40 +/- 2.77)% and (26.88 +/- 3.79)% in group I and II, which were significantly higher than that in group III (18.58 +/- 4.04)% (P < 0.05, P < 0.01), CD16+ were (8.98 +/- 2.18)% and (10.84 +/- 2.51)% in group I and II, which were significantly higher than that in group III (6.34 +/- 2.01)% (P < 0.01, P < 0.001). The expression of TNF-alpha in group I and II were higher than that of group III, TGF-beta in group I and II were lower than that of group III, but there was no significant difference (P > 0.05). The expression of CD3+, CD8+, CD4+/ CD8+ ratio were not significant difference among the three groups (P > 0.05).
CONCLUSIONS: Mifepristone with misoprostol for terminating early pnegnancy might be affect the expression of lymphocyte and cytokines and induce the disorder of decidual micro-environment which might be the reason of medical abortion.

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Year:  2001        PMID: 16134529

Source DB:  PubMed          Journal:  Zhonghua Fu Chan Ke Za Zhi        ISSN: 0529-567X


  2 in total

1.  The immunological effect of Galectin-9/TIM-3 pathway after low dose Mifepristone treatment in mice at 14.5 day of pregnancy.

Authors:  Adrienn Lajko; Matyas Meggyes; Beata Polgar; Laszlo Szereday
Journal:  PLoS One       Date:  2018-03-22       Impact factor: 3.240

2.  Mifepristone increases the cytotoxicity of uterine natural killer cells by acting as a glucocorticoid antagonist via ERK activation.

Authors:  Yuezhou Chen; Yan Wang; Yaling Zhuang; Feng Zhou; Lili Huang
Journal:  PLoS One       Date:  2012-05-01       Impact factor: 3.240

  2 in total

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