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Updated: Apr 10, 2026

Isolation of Leukocytes from the Murine Tissues at the Maternal-Fetal Interface
Published on: May 21, 2015
Balancing IL-17: Implications for immune tolerance, pregnancy outcomes, and reproductive health
Jarupa Soongsathitanon1, Sutatip Pongcharoen2
1Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Abstract:
Interleukin-17 (IL-17), a pro-inflammatory cytokine best known for its role in autoimmune disease, has emerged as a key immunomodulator in pregnancy. Its presence at the maternal-fetal interface reflects a finely tuned balance in which IL-17 contributes not only to host defense and tissue remodeling but also to processes essential for early gestation, including trophoblast invasion, angiogenesis, and immune tolerance. However, excessive or dysregulated IL-17 activity is linked to adverse pregnancy outcomes such as preeclampsia, preterm labor, miscarriage, and fetal growth restriction. IL-17 is also implicated in pregnancy-related manifestations of maternal autoimmune diseases, highlighting its relevance in both maternal health and fetal development. This review synthesizes current evidence on the physiological and pathological roles of IL-17 across the menstrual cycle and pregnancy, integrates findings from human and animal studies, and discusses emerging clinical applications, including its potential as a biomarker and therapeutic target in infertility and assisted reproductive technologies. Understanding the context-dependent actions of IL-17 may provide new opportunities to improve reproductive outcomes and guide future translational research in reproductive immunology.
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