机构地区:[1]浙江大学医学院附属妇产科医院计划生育科,杭州310006
出 处:《中华妇产科杂志》2007年第12期826-829,共4页Chinese Journal of Obstetrics and Gynecology
摘 要:目的探讨低剂量米非司酮对植入窗口期子宫内膜中子宫自然杀伤(uNK)细胞数量及其亚型含量的影响。方法收集正常妇女植入窗口期的子宫内膜14份,将每份内膜组织平均分为3部分,分别用浓度为65 nmol/L 米非司酮(A 组)、200 nmol/L 米非司酮(B 组)和0 nmol/L 米非司酮(对照组)进行体外培养,运用免疫组化和流式细胞技术检测 uNK 细胞数量及 CD_3^-CD_(56)^+CD_(16)^-亚型、CD_3^-CD_(56)^+CD_(16)^+亚型的百分含量。结果 (1)A、B 及对照组子宫内膜中 CD_(56)^+uNK 细胞数量分别为(148±11)、(150±12)和(121±7)个,A、B 组分别与对照组比较,差异均有统计学意义(P<0.05);A、B 组之间比较,差异无统计学意义(P>0.05)。(2)A 组和 B 组子宫内膜中 CD_3^-CD_(56)^+亚型百分含量分别为(44±5)%和(48±4)%,高于对照组[(35±3)%],差异有统计学意义(P<0.05),A、B 组间比较,差异无统计学意义(P>0.05);A 组和 B 组子宫内膜 CD_3^-CD_(56)^+CD_(16)^-亚型百分含量分别为(42±5)%和(45±5)%,高于对照组[(33±3)%],差异有统计学意义(P<0.05),A、B 组间比较,差异无统计学意义(P>0.05);CD_3^-CD_(56)^+CD_(16)^+亚型百分含量分别为(2.70±0.24)%、(3.26±0.37)%和(2.33±0.29)%,3组间比较,差异无统计学意义(P>0.05)。结论低剂量米非司酮可通过增加uNK 细胞数量及 CD_3^-CD_(56)^+CD_(16)^-亚型百分含量,使植入窗口期子宫内膜局部免疫微环境失平衡,从而可能导致胚胎植入的失败。Objective To investigate the immunologic mechanism of low dose mifepristone as an anti-implantation contraceptive drug. Methods Endometrial biopsies were obtained from fourteen normally cycling women during the receptive phase. Each endometrial tissue, divided into three equal parts, was assigned to three groups: control group, 65 nmol/L mifepristone group (group A ) and 200 nmol/L mifepristone group (group B). Endometrial explants were cultured in vitro. The numbers of natural killer cells and the percentages of CD3^-CD56^+CD16^- subset and CD3^-CD56^+CD16^+ subset were analysed by immunohistochemistry and flow cytometry. Results ( 1 ) The mean number of CD56^+ NK cells in group A (148 ± 11 ) and group B( 150 ± 12) were significantly higher when compared to the control group( 121 ±7, P 〈 0. 05 ). There was no significant difference between the two mifepristone-treated groups ( P 〉 0. 05 ). (2) The percentage of CD3^-CD56^+ NK cells in group A (44 ± 5 )% and in group B (48 ± 4 )% were significantly higher when compared to the control group (35 ± 3 ) % , ( P 〈 0. 05 ) , there was no significantly difference between the two mifepristone-treated groups ( P 〉 0. 05 ) ; The percentage of CD3^-CD56^+CD16^- subset in group A (42 ±5)% and in group B(45 ± 5)% were significantly higher when compared to the control group (33 ± 3 ) % , ( P 〈 0. 05 ), there was no significantly difference between the two mifepristone-treated groups ( P 〉 0. 05 ) ; the percentages of CD3^-CD56^+CD16^+ subset in three groups [ ( 2.70 ± 0. 24 ) %, ( 3. 26 ± 0. 37 ) % and (2. 33 ± 0.29)% ] were not significantly different (P 〉 0. 05) . Conclusion Low dose mifepristones increase the number of CD56^+ NK cells and the percentage of CD3^-CD56^+CD16^- NK subset, which might result in the disturbance of human endometrial immuno-microenvironment during receptive phase and lead to implantation failure.
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