IL-17 Induces Fetal Loss in a CBA/JBALB/c Mouse Model, and an Anti-IL-17 Antibody Prevents Fetal Loss in a CBA/J DBA/2 Mouse Model

Problem Many researchers have demonstrated that the expression of interleukin-17(IL-17) is higher in spontaneous abortion. However, whether Th17 cells are an independent factor in inducing abortion is not known. Method of study This study investigated the effect of exogenous recombinant IL-17 and an...

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Veröffentlicht in:American journal of reproductive immunology (1989) 2016-01, Vol.75 (1), p.51-58
Hauptverfasser: Xu, Wang-Ming, Xiao, Zhuo-Ni, Wang, Xiao-Bo, Huang, Ying
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Sprache:eng
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Zusammenfassung:Problem Many researchers have demonstrated that the expression of interleukin-17(IL-17) is higher in spontaneous abortion. However, whether Th17 cells are an independent factor in inducing abortion is not known. Method of study This study investigated the effect of exogenous recombinant IL-17 and an anti-IL-17 antibody in a normal and an abortion mouse model using flow cytometry, enzyme-linked immunosorbent assay, real-time PCR, and Western blot. Results Th17 cells and the related factors, IL-17 and ROR gamma t, were significantly upregulated in abortion mice, and Treg cells and the related factor, Foxp3, were downregulated. Intraperitoneal injection of recombinant IL (rIL)-17 induced fetal loss in a normal mouse model, and an anti-IL-17 antibody prevented fetal loss in an abortion mouse model. Conclusion This study confirmed an imbalance of the Th17/Treg paradigm in abortion mice and IL-17 as a risk factor of fetal loss. An anti-IL-17 antibody may prevent abortion.
ISSN:1046-7408
1600-0897
DOI:10.1111/aji.12437