NK and T Cell Subtypes in the Endometrium of Patients with Recurrent Pregnancy Loss and Recurrent Implantation Failure: Implications for Pregnancy Success

被引:9
作者
Braun, Anne-Sophie [1 ]
Vomstein, Kilian [1 ,2 ,3 ,4 ]
Reiser, Elisabeth [1 ]
Tollinger, Susanne [1 ]
Kyvelidou, Christiana [1 ]
Feil, Katharina [1 ]
Toth, Bettina [1 ]
机构
[1] Med Univ Innsbruck, Dept Gynecol Endocrinol & Reprod Med, Anichstr 35, A-6020 Innsbruck, Austria
[2] Copenhagen Univ Hosp Hvidovre, Dept Obstet & Gynecol, Fertil Clin, Kettegard Alle 30, DK-2650 Hvidovre, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Recurrent Pregnancy Loss Unit, DK-2100 Copenhagen, Denmark
[4] Hvidovre Univ Hosp, DK-2100 Copenhagen, Denmark
基金
奥地利科学基金会;
关键词
reproductive immunology; uterine NK cells; immunophenotype; endometrium; miscarriage; NATURAL-KILLER-CELLS;
D O I
10.3390/jcm12175585
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: RPL and RIF are challenges in reproductive medicine. The immune system plays a pivotal role in endometrial receptivity, successful implantation, and pregnancy complications. Immunological changes have been associated with RPL and RIF. Understanding immune dysregulation especially in NK and T cell subtypes may lead to better diagnostic concepts and treatments. From July 2019 to August 2020 patients with RPL and RIF underwent a standardized diagnostic procedure including endometrial biopsies. Immune cell analysis was performed using flow cytometry. Patients were contacted in March 2023 and interviewed concerning their pregnancy outcomes following diagnostics. Results: Out of 68 patients undergoing endometrial biopsies, 49 patients were finally included. Live birth rates were high with 72% in RPL and 86% in RIF. Immune cell analysis revealed that patients with RPL had more cytotoxic CD56dimCD16high cells, while RIF patients had more CD56+ uNK cells. RPL patients with pregnancy complications showed increased NKT cell percentages. Conclusion: Our findings suggest specific immune changes in RPL and RIF patients, offering potential therapeutic targets. Tailored immunotherapy based on endometrial immunophenotyping might be an option, but further research is needed.
引用
收藏
页数:12
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