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To investigate the expression of Siglec10 and CD24 in normal early pregnancy and missed abortion, and their significance in the maternal-fetal interface. For our research, we employed Q-PCR and WB techniques to evaluate the traits and expression of Siglec10 and CD24 in the nonpregnant endometrium, as well as in the villus and decidua of women in their 6–10 weeks of normal early pregnancy and those who experienced missed abortion. Additionally, we utilized ELISA to determine the levels of Siglec10 and CD24 in the peripheral blood of pregnancy, missed abortion, and non-pregnant individuals. T-test and ANOVA were used to compare groups. 1. Villous tissues in early pregnancy showed high expression of Siglec10 and CD24, with a significant increase in expression in the missed abortion group ( P  &lt; 0.01). 2. Nonpregnant endometrial tissue showed low expression of Siglec10 and CD24, while early pregnancy decidua showed high expression, with even higher expression in missed abortion (all  P  &lt; 0.05). 3. Serum levels of Siglec10 and CD24 in normal early pregnancy were significantly higher than non-pregnancy ( P  &lt; 0.01). However, the missed abortion group showed significantly higher levels than normal pregnancy ( P  &lt; 0.01). 4. CD24 expression in serum of missed abortion increases with Siglec10 expression, indicating a significant positive correlation ( r  = 0.500,  P  &lt; 0.01). Siglec10 and CD24 expression in villus, decidua, and peripheral blood are up-regulated in unexplained missed abortions than those of women with normal pregnancies. This suggests that the levels of serum Siglec10 and CD24 can be used as an effective predictor of missed abortion.

High Expression and Significance of Siglec10/CD24 in Unexplained Missed Abortion