Department of Obstetrics and Gynecology, Hirosaki University Graduate School of Medicine, Hirosaki, Aomori 036-8562, Japan.
Am J Reprod Immunol. 2009 Dec;62(6):371-80. doi: 10.1111/j.1600-0897.2009.00750.x. Epub 2009 Oct 11.
Natural cytotoxicity receptors (NCRs) are unique markers, which regulate NK cell cytotoxicity and cytokine production. We investigated whether women with recurrent pregnancy losses (RPLs) and implantation failures have aberrant correlation between NCRs and intracellular cytokine expression of NK cells.
Peripheral blood NK cells (CD56(dim) and CD56(bright)) were analyzed for NCRs (NKp46, NKp44 and NKp30) and cytokine expression (TNF-alpha, IFN-gamma, IL-4, IL-10) using flow cytometry in RPL (n = 22), implantation failures (n = 23) or controls (n = 15).
In type 1 cytokine studies, CD56(bright)/NKp30(+) cells in controls (r = 0.696, P < 0.05) were positively correlated with CD56(bright)/IFN-gamma(+)/TNF-alpha(+) cells. CD56(bright)/NKp46(+) cells in implantation failures (r = -0.76, P < 0.01) were negatively correlated with CD56(bright)/IFN-gamma(+)/TNF-alpha(-) cells. RPL did not have any correlation. In type 2 cytokine studies, CD56(+)/NKp46(+) cells (r = 0.758, P < 0.01) and CD56(+)/NKp30(+) cells (r = 0.637, P < 0.05) were positively correlated with CD56(bright)/IL-4(+)/IL-10(+) cells in controls. CD56(+)/NKp30(+) cells in implantation failures (r = -0.778, P < 0.05) were negatively correlated with CD56(bright)/IL-10(+)/IL-4(+) cells. There were no correlations in RPL.
Recurrent pregnancy losses and implantation failures have lack of, or negative correlation between NCRs and intracellular cytokines expression. This observation suggests that excessive pro-inflammatory cytokine expression in NK cells in RPL and implantation failures may be exerted through the NCRs or interruption of signal transduction processes.
自然细胞毒性受体(NCRs)是独特的标志物,可调节 NK 细胞的细胞毒性和细胞因子产生。我们研究了复发性妊娠丢失(RPL)和着床失败的女性是否存在 NCRs 与 NK 细胞细胞内细胞因子表达之间的异常相关性。
使用流式细胞术分析 RPL(n=22)、着床失败(n=23)或对照组(n=15)外周血 NK 细胞(CD56(dim)和 CD56(bright))的 NCRs(NKp46、NKp44 和 NKp30)和细胞因子表达(TNF-α、IFN-γ、IL-4、IL-10)。
在 1 型细胞因子研究中,对照组 CD56(bright)/NKp30(+)细胞(r=0.696,P<0.05)与 CD56(bright)/IFN-γ(+)/TNF-α(+)细胞呈正相关。着床失败 CD56(bright)/NKp46(+)细胞(r=-0.76,P<0.01)与 CD56(bright)/IFN-γ(+)/TNF-α(-)细胞呈负相关。RPL 没有相关性。在 2 型细胞因子研究中,CD56(+)/NKp46(+)细胞(r=0.758,P<0.01)和 CD56(+)/NKp30(+)细胞(r=0.637,P<0.05)与对照组 CD56(bright)/IL-4(+)/IL-10(+)细胞呈正相关。着床失败 CD56(+)/NKp30(+)细胞(r=-0.778,P<0.05)与 CD56(bright)/IL-10(+)/IL-4(+)细胞呈负相关。RPL 无相关性。
复发性妊娠丢失和着床失败的 NCRs 与细胞内细胞因子表达之间缺乏相关性或呈负相关。这一观察结果表明,RPL 和着床失败中 NK 细胞过度表达促炎细胞因子可能是通过 NCRs 或信号转导过程的中断来实现的。