Skip to content

Obstetrical History and Anti-HLA Antibodies Level

Obstetrical History and Anti-HLA Antibodies Level

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06021925
Acronym
OBS-HLA
Enrollment
6000
Registered
2023-09-01
Start date
2023-12-13
Completion date
2024-06-13
Last updated
2024-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anti-HLA Antibody, Blood Donors

Keywords

Obstetrical complications, Levels of anti-HLA antibody, Chronic histiocytic intervillositis

Brief summary

Chronic histiocytic intervillositis (CHI) is associated with severe and recurrent obstetrical complications. A link between anti-HLA Antibodies (Ab) and CHI has recently been established. At the Etablissement Français du Sang (EFS), donors who have already given birth once and have high levels of anti-HLA are excluded from donating apheresis platelets and therapeutic plasma to prevent TRALI (Transfusion Related Acute Lung Injury). No studies have examined the obstetrical history of these donors. The question is: is there an association between anti-HLA levels and obstetrical complications?

Detailed description

Chronic histiocytic intervillositis (CHI) is a rare condition with an incidence of around 5 in 10,000 pregnancies. It is defined by major infiltration of the intervillous cavity by CD68+ maternal histiocytes, associated with fibrin deposition on the villous surface. CHI is associated with severe obstetrical complications and a very high recurrence rate, estimated at between 70% and 100%. These complications include early and late miscarriage, fetal death, severe growth retardation in surviving fetuses, and premature delivery. The survival rate reported in the literature varies between 30% and 50%. Anti-HLA antibodies are present in 54% of pregnant women at the end of pregnancy, and their rate increases towards the end of pregnancy. The presence of HLA antibodies also increases with the number of pregnancies, and is found in up to 74% of cases after more than 2 deliveries. The research question concerns the existence of a statistically significant association between the presence of high levels of anti-HLA antibodies and the occurrence of one or more obstetric complications.

Interventions

OTHERObstetrical history

Selection of donors by EFS retrospectively on the basis of inclusion criteria. Information note sent by e-mail, non-opposition as well as a questionnaire to be completed online to obtain data on obstetrical history.

OTHERAnti-HLA Antibody tests

Analyze responses in relation to the results of the anti-HLA Antibody tests performed at the time of donation.

Sponsors

Etablissement Français du Sang (Nouvelle Aquitaine)
CollaboratorUNKNOWN
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Female blood donors who have been tested for anti-HLA antibodies in the context of TRALI prevention between 2010 and 2020 at EFS Nouvelle Aquitaine \[The donors meet the conditions of the Order of December 17, 2019 establishing the selection criteria for blood donors and are over 18 years old, are not protected persons and understand French well\] * Women who have already given birth at least once (non-nulliparous women) * Women who have not expressed their opposition at the time of donation to participating in a research project and to be contacted

Exclusion criteria

* None \[Donors meet the conditions of the Order of December 17, 2019 establishing the selection criteria for blood donors and are over 18 years old, are not protected persons and understand French well\]

Design outcomes

Primary

MeasureTime frameDescription
To measure the association between the occurrence of obstetrical complications and the level of anti-HLA Ab measured during the screening test performed by the EFS.2 monthsObstetrical complications are defined as (binomial qualitative variable) : * Preterm delivery \< 37 WA * Fetal death in utero whatever the term * Early or late miscarriage * Early or late pre-eclampsia * Medical termination of pregnancy * Intrauterine growth retardation \<3rd percentile

Secondary

MeasureTime frameDescription
Type and precocity of obstetrical complication (multinomial qualitative variable)2 months* Preterm deliveries \< 37 WA and ≥ 34 WA * Premature deliveries \< 34 WA * Fetal death in utero regardless of term * Late miscarriage \< 22 WA and ≥ 14 WA * Early miscarriage \< 14 WA * Late pre-eclampsia \> 37 WA and ≥ 34 WA * Early pre-eclampsia \< 34 WA * Medical termination of pregnancy * Intrauterine growth retardation \<3rd percentile
Measure the association between the type and precocity of obstetrical complications according to the type of anti-HLA Ab (class I and/or class II), when these Ab are found during the screening test performed by the EFS2 months* Preterm deliveries \< 37 WA and ≥ 34 WA * Premature deliveries \< 34 WA * Fetal death in utero regardless of term * Late miscarriage \< 22 WA and ≥ 14 WA * Early miscarriage \< 14 WA * Late pre-eclampsia \> 37 WA and ≥ 34 WA * Early pre-eclampsia \< 34 WA * Medical termination of pregnancy * Intrauterine growth retardation \<3rd percentile
Verify the absence of response bias by comparing the HLA Ab levels of responding versus non-responding donors.2 monthsAnti-HLA antibody rate (median)

Countries

France

Contacts

Primary ContactXavier LAFARGE, Doctor
xavier.lafarge@efs.sante.fr05 56 90 83 93
Backup ContactIsabelle JOLLET
isabelle.jollet@efs.sante.fr05 49 61 57 27

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026