{"title":"Immunological mechanisms and immunotherapeutic strategies for the maternal-fetal interface diseases during pregnancy","authors":"Shuo Zheng , Yulin Zhang , Yi Xing , Zhen Zhang , Yaqing Zhang , Liang Peng , Suya Chen , Yanli Zhang , Longquan Shao","doi":"10.1016/j.intimp.2026.116260","DOIUrl":null,"url":null,"abstract":"<div><div>The immune environment at the maternal-fetal interface is reliant on the precise regulation of various immune cells and their secreted cytokines, resulting in a coordinated balance of immune nutrition, immune defense, and immune tolerance to meet the needs of different stages of pregnancy. Disruption in the immunological microenvironment can lead to several pregnancy problems. In recent years, immunotherapy medications have made substantial advances in the treatment of maternal-fetal interface diseases during pregnancy. This paper provides a cellular and molecular review of the immunological mechanisms behind various common maternal-fetal interface diseases (preterm birth, recurring spontaneous abortion, preeclampsia, and fetal growth restriction). It offers a novel analysis of the mechanisms of action, application strategies, current research status, and future challenges for distinct immunotherapeutic agents from three separate perspectives: targeting different phases of inflammatory pathways, targeting particular immune cells at the maternal-fetal interface, and targeting specific autoantibodies associated with autoimmunity. The aim is to provide new insights for medication discovery, as well as precision diagnosis and treatment of pregnancy-related illnesses. These advancements will provide vital evidence for precision treatment of maternal-fetal interface diseases throughout pregnancy.</div></div>","PeriodicalId":13859,"journal":{"name":"International immunopharmacology","volume":"173 ","pages":"Article 116260"},"PeriodicalIF":5.6000,"publicationDate":"2026-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International immunopharmacology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567576926001037","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The immune environment at the maternal-fetal interface is reliant on the precise regulation of various immune cells and their secreted cytokines, resulting in a coordinated balance of immune nutrition, immune defense, and immune tolerance to meet the needs of different stages of pregnancy. Disruption in the immunological microenvironment can lead to several pregnancy problems. In recent years, immunotherapy medications have made substantial advances in the treatment of maternal-fetal interface diseases during pregnancy. This paper provides a cellular and molecular review of the immunological mechanisms behind various common maternal-fetal interface diseases (preterm birth, recurring spontaneous abortion, preeclampsia, and fetal growth restriction). It offers a novel analysis of the mechanisms of action, application strategies, current research status, and future challenges for distinct immunotherapeutic agents from three separate perspectives: targeting different phases of inflammatory pathways, targeting particular immune cells at the maternal-fetal interface, and targeting specific autoantibodies associated with autoimmunity. The aim is to provide new insights for medication discovery, as well as precision diagnosis and treatment of pregnancy-related illnesses. These advancements will provide vital evidence for precision treatment of maternal-fetal interface diseases throughout pregnancy.
期刊介绍:
International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome.
The subject material appropriate for submission includes:
• Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders.
• Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state.
• Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses.
• Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action.
• Agents that activate genes or modify transcription and translation within the immune response.
• Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active.
• Production, function and regulation of cytokines and their receptors.
• Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.