Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Department of Child and Adolescent Psychiatry, Erasmus Medical Center, Rotterdam, Netherlands.
Front Immunol. 2024 Mar 5;15:1350288. doi: 10.3389/fimmu.2024.1350288. eCollection 2024.
Disturbances in T-cells, specifically the Th17/Treg balance, have been implicated in adverse pregnancy outcomes. We investigated these two T-cell populations following pre-pregnancy and pregnancy SARS-CoV-2 infection and COVID-19 vaccination in 351 participants from a pregnancy cohort in New York City (Generation C; 2020-2022). SARS-CoV-2 infection status was determined via laboratory or medical diagnosis and COVID-19 vaccination status via survey and electronic medical records data. Peripheral blood mononuclear cells (PBMCs) were collected at routine prenatal visits throughout gestation (median 108 days; IQR 67-191 days) with repeated measures for 104 participants (29.6%). T-cell populations CD4+/CD3+, Th17/CD4+, Treg/CD4+ and the Th17/Treg ratio were quantified using flow cytometry. Results showed that inter-individual differences are a main influencing factor in Th17 and Treg variance, however total variance explained remained small (R = 15-39%). Overall, Th17 and Treg populations were not significantly affected by SARS-CoV-2 infection during pregnancy in adjusted linear mixed models (>0.05), however comparison of repeated measures among SARS-CoV-2 infected participants and non-infected controls suggests a relative increase of the Th17/Treg ratio following infection. In addition, the Th17/Treg ratio was significantly higher after SARS-CoV-2 infection prior to pregnancy (10-138 weeks) compared to controls (β=0.48, =0.003). COVID-19 vaccination was not associated with Th17 and Treg cells. Our findings suggest an impact of SARS-CoV-2 infection on the Th17/Treg ratio, likely depending on severity of infection, yet the observed trends and their potential consequences for pregnancy outcomes require further investigation. Our study contributes to growing evidence that COVID-19 vaccination during pregnancy does not lead to an exacerbated immune response.
T 细胞(尤其是 Th17/Treg 平衡)的紊乱与不良妊娠结局有关。我们在纽约市妊娠队列(Generation C;2020-2022 年)的 351 名参与者中研究了这两种 T 细胞群体在妊娠前和妊娠期间感染 SARS-CoV-2 以及接种 COVID-19 疫苗后的情况。通过实验室或医疗诊断确定 SARS-CoV-2 感染状况,通过调查和电子病历数据确定 COVID-19 疫苗接种状况。在整个妊娠期间(中位数 108 天;IQR 67-191 天)在常规产前就诊时采集外周血单核细胞(PBMC),对 104 名参与者(29.6%)进行重复测量。使用流式细胞术定量 CD4+/CD3+、Th17/CD4+、Treg/CD4+和 Th17/Treg 比值。结果表明,个体间差异是 Th17 和 Treg 变异的主要影响因素,但总方差解释仍然较小(R=15-39%)。总体而言,在调整后的线性混合模型中,SARS-CoV-2 感染在妊娠期间未显著影响 Th17 和 Treg 群体(>0.05),但对 SARS-CoV-2 感染参与者和未感染对照者的重复测量比较表明,感染后 Th17/Treg 比值相对增加。此外,与对照组相比,妊娠前(10-138 周)SARS-CoV-2 感染后 Th17/Treg 比值显著升高(β=0.48,=0.003)。COVID-19 疫苗接种与 Th17 和 Treg 细胞无关。我们的研究结果表明,SARS-CoV-2 感染对 Th17/Treg 比值有影响,可能取决于感染的严重程度,但观察到的趋势及其对妊娠结局的潜在影响需要进一步研究。我们的研究结果为越来越多的证据表明,妊娠期间接种 COVID-19 疫苗不会导致免疫反应加剧做出了贡献。