RecruitingNot ApplicableNCT03357172

Determination of Factors Involved in the Regulation of Immune Responses After Allogeneic Hematopoietic Stem Cell Transplantation


Sponsor

Central Hospital, Nancy, France

Enrollment

700 participants

Start Date

Oct 1, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The study concerns donors and patients receiving allogeneic stem cell haematopoietic transplantation. The aim of the study is to analyse HSC graft content in immune effector T (naive, memory, activated, exhausted) and immunoregulatory cell subtypes (Tregs, iNKT, MDSC) and correlate the results with post-transplant immune reconstitution of those different cell subtypes and clinical events (graft-versus-host-disease, relapse, infections). An ancillary study will focus on the impact of microbiota dysbiosis on post-transplant immune response and regulatory cell subsets.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • patient of the Nancy CHRU, for whom a CSH allograft is planned. or
  • hematopoietic stem cell donors received at Nancy's CHRU for the duration of the research

Exclusion Criteria2

  • Positive HIV
  • active hepatitis B or C infection

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BIOLOGICALBlood Sample

Additional blood sample before graft, D0, D7, D15, D21, D30, D60, D90, D180, Y1, Y2

BIOLOGICALBone marrow aspiration

Additional bone marrow aspiration before graft, D30, D90, Y1

BIOLOGICALBlood sample

Before donation

BIOLOGICALAllogeneic hematopoietic stem cell sample

Allogeneic hematopoietic stem cell sample


Locations(1)

CHRU de Nancy

Vandœuvre-lès-Nancy, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03357172


Related Trials