EFS, Recherche et Développement, Grenoble, France.
Université Grenoble-Alpes, INSERM U1209, CNRS UMR, Institute for Advanced Biosciences, Grenoble, France.
Front Immunol. 2023 Apr 4;14:1136749. doi: 10.3389/fimmu.2023.1136749. eCollection 2023.
Immune function in pregnancy is influenced by host-specific and environmental factors. This may impact fetal immune development, but the link between maternal and neonatal immune function is still poorly characterized. Here, we investigate the relationship between maternal and neonatal immune function, and identify factors affecting the association between maternal and child cytokine secretion.
In the French prospective cohort SEPAGES, blood samples were obtained from pregnant women (n=322) at gestational week 20 ± 4 and from their child at birth (n=156). Maternal and cord blood cytokine and chemokine (CK) levels were measured at baseline in all subjects and after T cell or dendritic cell activation with phytohemagglutinin or R848 (in total 29 and 27 measures in maternal and cord blood samples, respectively). Associations between environmental, individual factors and CK level were estimated by linear regression modeling. The maternal-cord blood CK relations were assessed by Pearson correlation and regression models.
We observed that pregnant women and neonates displayed specific CK secretion profiles in the innate and adaptive compartments at baseline and upon activation. Activation of T cells in cord blood induced high levels of IL-2, but low levels of IFNγ, IL-13 or IL-10, in comparison to maternal blood samples. Elsewhere, neonatal innate immune responses were characterized by low production of IFNα, while productions of IL-1β, IL-6, IL-8, IL-10 and TNFα were higher than maternal responses. Strong correlations were observed between most CK after activation in maternal and cord blood samples. Strikingly, a statistical association between global mother and child cytokine profiles was evidenced. Correlations were observed between some individual CK of pregnant women and their children, both at baseline (MCP1, RANTES) and after activation with R848 (IL-6, IL-8 and IL-10). We looked for factors which could influence cytokine secretion in maternal or cord blood, and found that leucocyte counts, maternal age, pre-conception BMI, smoking and season were associated with the levels of several CK in mothers or children.
Our study reveals immune imprinting influencing immune responses in infants, opening the way to investigate the mechanisms responsible for this imprinting. Whether such influences have long lasting effects on children health warrants further investigation.
妊娠期间的免疫功能受宿主特异性和环境因素的影响。这可能会影响胎儿的免疫发育,但母体和新生儿免疫功能之间的联系仍未得到充分描述。在这里,我们研究了母体和新生儿免疫功能之间的关系,并确定了影响母体和儿童细胞因子分泌之间关联的因素。
在法国前瞻性队列 SEPAGES 中,在妊娠 20 ± 4 周时从孕妇(n=322)和分娩时从他们的孩子(n=156)获得血样。在所有受试者中,在基线时测量了母体和脐带血细胞因子和趋化因子(CK)水平,在用植物血凝素或 R848 激活后(分别在母体和脐带血样本中进行了 29 和 27 项测量)。通过线性回归模型估计了环境、个体因素与 CK 水平之间的关系。通过 Pearson 相关和回归模型评估了母血与脐血 CK 之间的关系。
我们观察到孕妇和新生儿在基线和激活时在先天和适应性免疫中表现出特定的 CK 分泌谱。与母血样本相比,脐带血中 T 细胞的激活诱导了高水平的 IL-2,但低水平的 IFNγ、IL-13 或 IL-10。此外,新生儿先天免疫反应的特点是 IFNα产生较低,而 IL-1β、IL-6、IL-8、IL-10 和 TNFα的产生高于母体反应。在母体和脐带血样本中,激活后大多数 CK 之间存在强烈的相关性。值得注意的是,在母体和儿童细胞因子谱之间观察到了统计学关联。在基线(MCP1、RANTES)和用 R848 激活后(IL-6、IL-8 和 IL-10)观察到孕妇和她们孩子之间的一些个体 CK 之间存在相关性。我们寻找可能影响母体或脐带血中细胞因子分泌的因素,发现白细胞计数、母亲年龄、孕前 BMI、吸烟和季节与母亲或孩子的几种 CK 水平相关。
我们的研究揭示了影响婴儿免疫反应的免疫印迹,为研究这种印迹的机制开辟了道路。这种影响是否对儿童健康有长期影响还有待进一步研究。