Omics approaches: interactions at the maternal-fetal interface and origins of child health and disease

被引:13
作者
Ozen, Maide [1 ]
Aghaeepour, Nima [2 ,3 ,4 ]
Maric, Ivana [3 ]
Wong, Ronald J. [3 ]
Stevenson, David K. [3 ]
Jantzie, Lauren L. [1 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pediat, Div Neonatal Perinatal Med, Baltimore, MD 21205 USA
[2] Stanford Univ, Dept Anesthesiol Pain & Perioperat Med, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pediat, Div Neonatal & Dev Med, Sch Med, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Biomed Data Sci, Sch Med, Stanford, CA 94305 USA
[5] Johns Hopkins Univ, Sch Med, Kennedy Krieger Inst, Baltimore, MD USA
关键词
NF-KAPPA-B; HEART-RATE CHARACTERISTICS; NECROSIS-FACTOR-ALPHA; REGULATORY T-CELLS; BRONCHOPULMONARY DYSPLASIA; INFLAMMATORY RESPONSE; PATHOLOGICAL FEATURES; IMMUNE-RESPONSES; CHORIOAMNIONITIS; PRETERM;
D O I
10.1038/s41390-022-02335-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Immunoperinatology is an emerging field. Transdisciplinary efforts by physicians, physician-scientists, basic science researchers, and computational biologists have made substantial advancements by identifying unique immunologic signatures of specific diseases, discovering innovative preventative or treatment strategies, and establishing foundations for individualized neonatal intensive care of the most vulnerable neonates. In this review, we summarize the immunobiology and immunopathology of pregnancy, highlight omics approaches to study the maternal-fetal interface, and their contributions to pregnancy health. We examined the importance of transdisciplinary, multiomic (such as genomics, transcriptomics, proteomics, metabolomics, and immunomics) and machine-learning strategies in unraveling the mechanisms of adverse pregnancy, neonatal, and childhood outcomes and how they can guide the development of novel therapies to improve maternal and neonatal health. Impact Discuss immunoperinatology research from the lens of omics and machine-learning approaches. Identify opportunities for omics-based approaches to delineate infection/inflammation-associated maternal, neonatal, and later life adverse outcomes (e.g., histologic chorioamnionitis [HCA]).
引用
收藏
页码:366 / 375
页数:10
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