Department of Obstetrics and Gynecology, Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Fertil Steril. 2010 Nov;94(6):2244-7. doi: 10.1016/j.fertnstert.2009.11.020. Epub 2010 Jan 8.
To investigate the proportions of CD4+CD25high T cells and forkhead box p3 (FOXP3) expression in peripheral blood and decidua in patients with unexplained recurrent spontaneous abortion (URSA).
Prospective clinical study.
University hospital.
PATIENT(S): 125 URSA patients, 35 normal early pregnant women, and 28 normal nonpregnant women.
INTERVENTION(S): Measurements of CD4+CD25high T cells and FOXP3 expression in peripheral blood and decidua.
MAIN OUTCOME MEASURE(S): The proportions of CD4+CD25high T cells and FOXP3 expression.
RESULT(S): In peripheral blood, statistically significantly higher proportions of CD4+CD25high T cells and FOXP3 expression were observed in normal early pregnant women compared with normal nonpregnant women and URSA patients; a statistically significantly lower proportion of CD4+CD25high T cells was observed in nonpregnant URSA patients compared with URSA patients who had early miscarriages and normal nonpregnant women. In the decidua, statistically significantly lower proportions of CD4+CD25high T cells and FOXP3 expression were found in URSA patients with early miscarriages compared with normal early pregnant women.
CONCLUSION(S): The CD4+CD25high T cells may play an important role in maintaining a normal pregnancy. The reduction in CD4+CD25high T cells may involve in the pathogenesis of URSA, and is correlated with lower FOXP3 expression.
研究原因不明复发性自然流产(URSA)患者外周血和蜕膜中 CD4+CD25highT 细胞及叉头框 P3(FOXP3)表达的比例。
前瞻性临床研究。
大学医院。
125 例 URSA 患者,35 例正常早孕妇女和 28 例正常非妊娠妇女。
测量外周血和蜕膜中 CD4+CD25highT 细胞及 FOXP3 的表达。
CD4+CD25highT 细胞及 FOXP3 的表达比例。
在外周血中,正常早孕妇女 CD4+CD25highT 细胞及 FOXP3 的表达比例明显高于正常非妊娠妇女和 URSA 患者;而非妊娠 URSA 患者 CD4+CD25highT 细胞的比例明显低于早期流产的 URSA 患者和正常非妊娠妇女。在蜕膜中,早期流产的 URSA 患者 CD4+CD25highT 细胞及 FOXP3 的表达比例明显低于正常早孕妇女。
CD4+CD25highT 细胞可能在维持正常妊娠中起重要作用。CD4+CD25highT 细胞的减少可能与 URSA 的发病机制有关,并与 FOXP3 表达降低相关。