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临床试验/NCT05689905
NCT05689905已完成不适用

Immunologic Risk of Pregnancy in Women With Lung Transplant

Nantes University Hospital9 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2024年2月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
11
试验地点
9
主要终点
Risk of humoral rejection if common HLA antigen between child and graft.

研究概览

简要总结

TRIGGER 1 is a previous study that evaluate the immunological risk of pregnancy in women with lung transplants in France, whose pregnancy has ended between January 1, 2012 and December 31, 2021. The primary endpoint is the occurrence of humoral rejection with a year after pregnancy.

TRIGGER 2 aims to evaluate the risk of humoral rejection if there are common antigens between the child and the lung donor. We will collect HLA typing from children to compare them to the HLA typing of the mother, the lung donor and the antibodies produced if there are.

Thus, it will help us to suggest recommendations to limit the immunological risk of pregnancy for lung transplant women.

Lung transplantation is the treatment of choice of terminal chronic respiratory failure, such as cystic fibrosis and pulmonary hypertension. Young female patient of childbearing age are concerned.

For many years, given the risk of maternal and fetal complications, pregnancies were not recommended. Studies on large cohorts of transplanted patients, particularly kidney transplanted patients, have made it possible to study the risks of maternal, obstetrical and neonatal complications.

A few studies have been published in lung transplantation on small numbers of patients. However, these publications reporting on the fate of pregnancies in cohorts of lung transplant patients do not mentioned the immunological risk, with in particular the absence of studies on the risk of humoral rejection, appearance of anti-HLA (Human Leukocyte Antigens) antibodies (Ac) and the possible appearance of anti-HLA Ac directed against the donor (donor specific antibody, DSA).

TRIGGER 1 is a previous study, whose main objective is to evaluate the immunological risk of pregnancy in women with lung transplants (mono-, bi-, or cardiopulmonary) in France, whose pregnancy has ended between January 1, 2012 and December 31, 2021. The primary endpoint is the occurrence of humoral rejection within 1 year after pregnancy.

For this study TRIGGER2, we will collect the HLA typing of the children for pregnancies that resulted in the birth of a child. Thus, we will be able to compare the HLA typing of the children with the HLA typings of the mother and the lung donor, and the antibodies produced by the mother. The primary endpoint is to evaluate the risk of humoral rejection if there are common HLA antigens between the child and the lung donor.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
1 Year 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Children born between 01/01/2012 and 31/12/2021 of female patients over 18 years old with lung transplantation (mono, uni or cardio pulmonary) in France,
  • •Alive at the time of our study.
  • •Legal guardians' consent for oral swabbing of their child and HLA typing on this swab
  • •Affiliated or beneficiaries of a social security system or similar

排除标准

  • •- Refusal of consent by the patient and/or one of the two parents

研究组 & 干预措施

Common HLA antigens with the lung donor

Children who have common HLA antigens with the lung donor of their mother

干预措施: HLA typing of the children (Diagnostic Test)

No common HLA antigens with the lung donor

Children without common HLA antigens with the lung donor of their mother.

干预措施: HLA typing of the children (Diagnostic Test)

结局指标

主要结局

Risk of humoral rejection if common HLA antigen between child and graft.

时间窗: Baseline

Identification of common HLA antigen between child and graft by HLA typing

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (9)

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