Gregory C D, Shah L P, Lee H, Scott I V, Golding P R
J Clin Lab Immunol. 1985 Dec;18(4):175-81.
A longitudinal analysis of natural killer (NK) cell-mediated cytotoxicity of maternal peripheral blood lymphocytes was carried out at various stages (16-36 weeks) of normal human pregnancy, within 1 week following delivery and up to 40 weeks post-partum. NK cell-mediated lysis of K562 target cells (TC) in short term 51Cr-release assays was significantly depressed throughout pregnancy, returning to control levels 9-40 weeks post-partum. Natural cytotoxicity of unseparated maternal peripheral blood was also substantially depressed at all stages of pregnancy and, in addition, remained impaired in the late post-partum period. Longitudinal enumeration of Leu 3a+ and Leu 2a+ lymphocytes indicated an absence of helper/suppressor T-cell imbalance during pregnancy, and analysis of Leu 7+ cells showed no difference in population sizes between control and pregnancy groups. Comparison of blood and lymphocyte cytotoxicity in control and pregnancy samples suggested a complex regulation of NK reactivity during pregnancy. The potential role in vivo of both plasma-associated and cellular regulatory elements is discussed.
对正常人类妊娠各阶段(16 - 36周)、分娩后1周内及产后40周内母体外周血淋巴细胞自然杀伤(NK)细胞介导的细胞毒性进行了纵向分析。在短期51Cr释放试验中,整个孕期NK细胞介导的对K562靶细胞(TC)的裂解显著降低,产后9 - 40周恢复至对照水平。未分离的母体外周血的自然细胞毒性在妊娠各阶段也大幅降低,此外,在产后晚期仍受损。对Leu 3a +和Leu 2a +淋巴细胞的纵向计数表明孕期不存在辅助/抑制性T细胞失衡,对Leu 7 +细胞的分析显示对照组和妊娠组细胞群体大小无差异。对照样本和妊娠样本中血液及淋巴细胞细胞毒性的比较表明孕期NK反应性存在复杂调节。讨论了血浆相关和细胞调节元件在体内的潜在作用。