Buchanan Christopher Q, Lawlor Megan L, Okafor Chukwuebuka, Kurian Shannon R, Philip Andrea E, Finkle Abigael E, McQuillan Jay J, Haridas Seema, Koenig Joyce M
Department of Obstetrics, Gynecology and Women's Health, Division of Maternal-Fetal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Department of Pediatrics, Division of Neonatal-Perinatal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Newborn (Clarksville). 2023 Apr-Jun;2(2):133-141. doi: 10.5005/jp-journals-11002-0064. Epub 2023 May 7.
Maternal-fetal immune crosstalk mechanisms are increasingly identified in the pathogenesis of gestational disorders, including histologic chorioamnionitis (HCA). Although an inflammatory Th17 immune phenotype has been described in preterm neonates with HCA, the associated maternal Th17 response is relatively unknown. To refine our understanding of Th17 biology in this context, we examined Th17 responses in maternal-cord blood dyads of preterm gestations.
Paired maternal and cord blood (CB) samples were prospectively collected from preterm gestations (23-34 weeks) with HCA or controls. Th17-linked cell frequencies and plasma calgranulin (S100A8, S100A12) levels were determined by flow cytometry and enzyme-linked immunoassay, respectively.
Analyses of 47 maternal-cord blood pairs showed striking parallel increases in Th17 cell frequencies as well as plasma calgranulin levels in the presence of fetal inflammation. Cord blood S100A12 levels were directly correlated with Th17 cell frequencies. In CB cultures, rh-S100A12 promoted propagation of Th17-type CD4 cells.
Maternal and CB Th17-linked responses are dually amplified in gestations with HCA, supporting a biological role for maternal-fetal interactions in this disorder. In addition to advancing current knowledge of neonatal Th17 mechanisms, these data shed new light on their association with maternal inflammation.
母婴免疫串扰机制在包括组织学绒毛膜羊膜炎(HCA)在内的妊娠疾病发病机制中日益被发现。尽管在患有HCA的早产新生儿中已描述了炎症性Th17免疫表型,但相关的母体Th17反应相对未知。为了在这种情况下完善我们对Th17生物学的理解,我们研究了早产妊娠母婴血对中的Th17反应。
前瞻性收集患有HCA的早产妊娠(23 - 34周)或对照的配对母血和脐血(CB)样本。分别通过流式细胞术和酶联免疫吸附测定法测定与Th17相关的细胞频率和血浆钙粒蛋白(S100A8、S100A12)水平。
对47对母婴血对的分析显示,在存在胎儿炎症的情况下,Th17细胞频率以及血浆钙粒蛋白水平显著平行升高。脐血S100A12水平与Th17细胞频率直接相关。在CB培养物中,重组人S100A12促进Th17型CD4细胞的增殖。
在患有HCA的妊娠中,母体和CB中与Th17相关的反应均被双重放大,支持母婴相互作用在这种疾病中的生物学作用。除了推进当前对新生儿Th17机制的认识外,这些数据还为它们与母体炎症的关联提供了新的线索。