Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON, Canada.
Department of Obstetrics & Gynecology, University of Toronto, Toronto, ON, Canada.
J Cell Mol Med. 2017 Oct;21(10):2386-2402. doi: 10.1111/jcmm.13160. Epub 2017 Apr 21.
The onset of labour in rodents and in humans is associated with physiological inflammation which is manifested by infiltration of activated maternal peripheral leukocytes (mPLs) into uterine tissues. Here, we used flow cytometry to immunophenotype mPLs throughout gestation and labour, both term and preterm. Peripheral blood was collected from non-pregnant women and pregnant women in the 1st, 2nd and 3rd trimesters. Samples were also collected from women in active labour at term (TL) or preterm (PTL) and compared with women term not-in-labour (TNIL) and preterm not-in-labour (PTNIL). Different leukocyte populations were identified by surface markers such as CD45, CD14, CD15, CD3, CD4, CD8, CD19 and CD56. Their activation status was measured by the expression levels of CD11b, CD44, CD55, CD181 and CD192 proteins. Of all circulating CD45+ leukocytes, we detected significant increases in CD15+ granulocytes (i) in pregnant women versus non-pregnant; (ii) in TL women versus TNIL and versus pregnant women in the 1st/2nd/3rd trimester; (iii) in PTL women versus PTNIL. TL was characterized by (iv) increased expressions of CD11b, CD55 and CD192 on granulocytes; (v) increased mean fluorescent intensity (MFI) of CD55 and CD192 on monocytes; (vi) increased CD44 MFI on CD3+ lymphocytes as compared to late gestation. In summary, we have identified sub-populations of mPLs that are specifically activated in association with gestation (granulocytes) or with the onset of labour (granulocytes, monocytes and lymphocytes). Additionally, beta regression analysis created a set of reference values to rank this association between immune markers of pregnancy and to identify activation status with potential prognostic and diagnostic capability.
分娩开始时,啮齿动物和人类的生理炎症与外周活化母体白细胞(mPL)浸润到子宫组织有关。在这里,我们使用流式细胞术对整个孕期和分娩(足月和早产)的 mPL 进行免疫表型分析。从非孕妇和妊娠 1、2、3 个月的孕妇中采集外周血。还从足月活跃分娩(TL)或早产活跃分娩(PTL)的妇女以及足月未分娩(TNIL)和早产未分娩(PTNIL)的妇女中采集样本,并与她们进行比较。不同的白细胞群通过表面标志物如 CD45、CD14、CD15、CD3、CD4、CD8、CD19 和 CD56 来识别。通过 CD11b、CD44、CD55、CD181 和 CD192 蛋白的表达水平来测量它们的激活状态。在所有循环 CD45+白细胞中,我们检测到 CD15+粒细胞(i)在孕妇与非孕妇之间;(ii)在 TL 妇女与 TNIL 妇女和与妊娠 1、2、3 个月的孕妇之间;(iii)在 PTL 妇女与 PTNIL 妇女之间显著增加。TL 的特点是(iv)粒细胞上 CD11b、CD55 和 CD192 的表达增加;(v)单核细胞上 CD55 和 CD192 的平均荧光强度(MFI)增加;(vi)与晚期妊娠相比,CD3+淋巴细胞上 CD44 的 MFI 增加。总之,我们已经确定了与妊娠(粒细胞)或分娩开始(粒细胞、单核细胞和淋巴细胞)相关的 mPL 的特定激活亚群。此外,贝叶斯回归分析创建了一组参考值,用于对妊娠免疫标志物之间的这种关联进行排序,并确定具有潜在预后和诊断能力的激活状态。