Intrauterine administration of autologous peripheral blood mononuclear cells regulates the endometrium estrogen and progesterone receptor expression: An RCT

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Intrauterine administration of autologous peripheral blood mononuclear cells significantly decreased endometrial estrogen receptor alpha and progesterone receptor expression during the implantation window in women with repeated implantation failure.

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This randomized clinical trial investigated the effects of intrauterine administration of autologous peripheral blood mononuclear cells on estrogen and progesterone receptor expression in women with repeated implantation failure. The study enrolled twenty-two participants who underwent endometrial biopsies to measure mRNA and protein levels of ERα and PR isoforms during the mid-secretory phase. Results indicated that PBMC treatment significantly downregulated the expression of ESR1, PGR, and PGRB compared to the control group, suggesting a mechanism for improved endometrial receptivity. Relevance to endometriosis: The paper explicitly excludes patients with endometriosis from its inclusion criteria, meaning it does not directly address the condition but rather focuses on unexplained repeated implantation failure in otherwise healthy uterine environments.

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Abstract

BACKGROUND: Repeated implantation failure (RIF) affects 15% of women of reproductive age. There is a high endometrial expression of both estrogen receptors and progesterone receptors (PRs) during the window of implantation in women with RIF. OBJECTIVE: To evaluate the effects of intrauterine administration of human peripheral blood mononuclear cells (PBMC) on estrogen receptor α (ERα) and PRs expression in the endometrium of women with RIF during the implantation window. MATERIALS AND METHODS: This randomized clinical trial study was conducted on 22 women with RIF history from January 2018 to August 2019 in Erfan hospital, Tehran, Iran. Participantswere divided into 2 groups (PBMC-treated group [n = 11] and control group [n = 11]). Endometrial tissue samples were collected at the implantation window time, during the mid-secretory phase (luteinizing hormone surge +7 days) of each menstrual cycle. The quantitative real-time polymerase chain reaction technique was used to measure the mRNA levels of ERα and PRs isoforms (PR-A and PR-B) in endometrial tissues. Furthermore, the protein expression of ERα and PRs was investigated using immunohistochemical staining. RESULTS: PBMC treatment significantly decreased the mRNA expression of endometrial ERα and PRs isoforms at the time of the implantation window (p < 0.001). Moreover, the endometrial ERα and PRs protein localization were significantly lower in PBMC-treated women compared with controls (p = 0.01, and p < 0.001 respectively). CONCLUSION: The intrauterine administration of PBMC decreased the endometrial ERα and PRs expression during the window of implantation in women with RIF. This local response to PBMC therapy could promote endometrial receptivity and embryo implantation.
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In conclusion, we provide new evidence demonstrating that the intrauterine administration of PBMC decreased the endometrial ERα and PR expression during the window of implantation in women with RIF. This local response to PBMC therapy could promote endometrial receptivity and embryo implantation.

Coi Statement

The authors declare that there is no conflict of interest.

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europepmc
last seen: 2026-10-11T09:27:45.537177+00:00
pubmed
last seen: 2026-10-08T21:39:52.685244+00:00
unpaywall
last seen: 2026-05-21T05:10:58.409756+00:00
License: CC-BY-NC-4.0