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Clinical Trials/NCT05648136
NCT05648136
Recruiting
Not Applicable

Immune Profile Analysis and Biomarker Identification in Women With Repeated Implantation Failure or Unexplained Recurrent Spontaneous Miscarriage

Centre Hospitalier Universitaire, Amiens1 site in 1 country150 target enrollmentDecember 2, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Repeated Embryo Implantation Failure
Sponsor
Centre Hospitalier Universitaire, Amiens
Enrollment
150
Locations
1
Primary Endpoint
Variation of the proportion of TH17 subpopulations between both patient groups
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Implantation is a determining step in human reproduction which requires the transition from a pro-inflammatory state to an anti-inflammatory state allowing the implantation of a competent embryo within a receptive endometrium, and then the maternal immunotolerance towards the alloantigenic fetus. Repeat implantation failures (RIFs), that refers to the fail to achieve a clinical pregnancy after the transfer of at least 3-4 good quality embryos or two blastocysts, and unexplained recurrent spontaneous miscarriage (RM) (≥2-3) could be related in some patients to immune imbalances characterized by an excessive and prolonged inflammatory response and/or a defect of anti-inflammatory regulation. In this context, several therapies have been evaluated in patients with RIFs or RMs in order to restore the immune balance, with heterogeneous results. No serum biomarker assay has been routinely approved to identify patients with immune imbalances that may explain repeated pregnancy failures and to predict the success of the subsequent IVF/ICSI cycle. The immunological analysis on peripheral blood will be based on the determination of the proportions of immune subpopulations (e.g. CD4+ et CD8+, TH1, TH2, TH17, Treg, ILC 1, ILC2, and ILC3) on the one hand and the circulating level of plasma cytokines on the other hand.

Registry
clinicaltrials.gov
Start Date
December 2, 2022
End Date
December 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • For patients :
  • Women aged 18 to 39 years
  • women with a history of RIF or unexplained RM
  • women with a negative diagnostic work-up (including pelvic ultrasound and hysteroscopy, parental karyotype, thyroid function test, and anti-thyroid and anti-phospholipid antibodies)
  • women with a basal FSH level \<10IU/l and AMH level \>1.5ng/ml
  • women with a regular menstrual cycle of 30+/-5 days
  • women receiving a new cycle of in vitro fertilization (IVF) +/- intracytoplasmic sperm injection (ICSI) for patients in the RIF group or a first cycle of IVF +/-ICSI for patients in the RM group
  • women received written and oral information and signed an informed consent
  • For control groups:
  • Controls recruited in the Obstetrics and Gynecology Department with at least one live birth after a spontaneous pregnancy (with a time to conception of less than 12 months for each pregnancy) Voluntary oocyte donors recruited within the CECOS de Picardie (having presented at least one live birth with a delay necessary to conceive of less than 12 months)

Exclusion Criteria

  • Ongoing pelvic and/or systemic infection
  • Chronic infectious endometritis
  • Active neoplasia
  • Autoimmune and autoinflammatory disease
  • Celiac disease
  • Thrombophilia (including positive anti-phospholipid antibodies)
  • Endocrine pathology (including dysthyroidism and diabetes)
  • Endometriosis
  • Polycystic ovary syndrome and ovulatory disorders
  • Premature ovarian failure

Outcomes

Primary Outcomes

Variation of the proportion of TH17 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of CD4+ subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of TH1 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of ILC 1 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of TH2 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of CD8+ subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of Treg subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of ILC 2 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of ILC 3 subpopulations between both patient groups

Time Frame: 18 months

Variation of the proportion of TNFα concentrations between both patient groups

Time Frame: 18 months

Variation of the proportion of IFN gamma concentrations between both patient groups

Time Frame: 18 months

Variation of the proportion of IL-17 concentrations between both patient groups

Time Frame: 18 months

Variation of the proportion of TGF-β concentrations between both patient groups

Time Frame: 18 months

Variation of the proportion of IL-10 concentrations between both patient groups

Time Frame: 18 months

Study Sites (1)

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