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早孕期至晚孕期正常妊娠蜕膜白细胞群体。

Decidual leucocyte populations in early to late gestation normal human pregnancy.

机构信息

Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom.

出版信息

J Reprod Immunol. 2009 Oct;82(1):24-31. doi: 10.1016/j.jri.2009.08.001. Epub 2009 Sep 3.

Abstract

Most research on human decidual leucocytes to date has focused on the predominant CD56+ uterine natural killer (uNK) cell population in early pregnancy. Few reports have documented decidual leucocyte populations after 13 weeks gestation and in late pregnancy. Placental bed (decidua basalis) and non-placental bed (decidua parietalis) biopsies from normal pregnancies were taken from women undergoing termination of pregnancy in the 1st and 2nd trimesters and following Caesarean section in the 3rd trimester. Immunohistochemistry was used to quantify the numbers of decidual cells expressing CD56, CD3, CD8, CD94, NKG2A and CD14 and double labelled CD161+CD3+ NKT-like cells. Although a significant reduction in CD56+ uNK cells was found in 3rd trimester samples compared with 1st and 2nd trimester decidua, a substantial residual CD56+ leucocyte population was identified in 3rd trimester decidua. Expression of the KIR CD94/NKG2A mirrored that of CD56 at all gestational ages, providing an explanation for the absence of cytotoxic responses at the fetal-maternal interface. There was no difference in leucocyte populations between decidua basalis and decidua parietalis. Double immunohistochemical labelling revealed small numbers of decidual CD3+CD56+ and CD8+CD56+ cells, which decreased in number at term, and CD161+CD3+ cells, which increased in number at term. No differences in leucocyte populations were detected between decidua parietalis and decidua basalis. In contrast to previous reports, a substantial residual CD56+ cell population was demonstrated in 3rd trimester decidua. Decidual cytotoxic T-lymphocytes did not alter in number during gestation, while in contrast CD14+ macrophages decreased at term, representing the smallest decidual population assessed.

摘要

迄今为止,大多数关于人类蜕膜白细胞的研究都集中在早孕时占主导地位的 CD56+子宫自然杀伤 (uNK) 细胞群上。很少有报道记录了 13 周妊娠后和晚期妊娠的蜕膜白细胞群。从接受 1 至 2 个月妊娠终止和 3 个月剖宫产的妇女中取出正常妊娠的胎盘床(底蜕膜)和非胎盘床(壁蜕膜)活检。免疫组织化学用于定量表达 CD56、CD3、CD8、CD94、NKG2A 和 CD14 的蜕膜细胞数量,并对 CD161+CD3+NKT 样细胞进行双标记。尽管与 1 至 2 个月的蜕膜相比,3 个月的样本中 CD56+uNK 细胞数量显著减少,但在 3 个月的蜕膜中仍发现了大量残留的 CD56+白细胞群。KIR CD94/NKG2A 的表达与所有妊娠年龄的 CD56 相似,这解释了在胎儿-母体界面不存在细胞毒性反应的原因。底蜕膜和壁蜕膜之间的白细胞群没有差异。双重免疫组织化学标记显示,蜕膜中 CD3+CD56+和 CD8+CD56+细胞数量较少,在足月时减少,CD161+CD3+细胞数量增加,在足月时增加。在壁蜕膜和底蜕膜之间未检测到白细胞群的差异。与之前的报道相反,在 3 个月的蜕膜中证明存在大量残留的 CD56+细胞群。在妊娠期间,蜕膜细胞毒性 T 淋巴细胞的数量没有改变,而相反,CD14+巨噬细胞在足月时减少,代表评估的最小蜕膜群体。

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