BIOCTA: Search Tolerance Signature in Vascularised Composite Allograft

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Completed
CT.gov ID
NCT02055521
Collaborator
ISTITUTO ITALIANO CHIRURGIA DELLA MANO, Italy (Other), medizinische universität innsbruck, Austria (Other), Hospital Clínico Universitario de Valencia (Other)
18
1
9
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Study Details

Study Description

Brief Summary

Composite tissue allotransplants (CTA) involve transplantation of various tissues including vessels, nerves, skin, bones, and immune cells and entail a significant antigenic load. The large majority of recipients have been maintained on immunosuppression therapy similar to that used in solid organ transplantation that is associated with the complications usually reported in solid organ transplantation. The question whether risks associated with indefinite immunosuppressive are justified for a non-lifesaving procedure still remains unanswered. At present no CTA recipient proved to be spontaneously tolerant with any immunosuppressive protocol; indeed, until now all recipients who discontinued the immunosuppressive therapy rejected their graft. On the other hand CTA recipients showed a low incidence of chronic rejection despite the high incidence of acute rejection episodes.

For all these reasons it should be of great interest to minimize the immunosuppression in CTA patients knowing their immunologic "risk". The main outcome of this study is to search for the signature of tolerance in recipients of hand or face allotransplantation testing biomarkers previously identified in operational tolerant kidney transplant recipients.

These markers have been developed studying tolerant kidney recipients and they were already tested in five bilateral hand transplantations and one face transplantation.

The present study will include hand and face allograft recipients transplanted at least one year in several European institutions (Innsbruck, Lyon, Monza, Valencia): 11 bilateral hand transplantations, 4 single hand transplantations and 3 face transplantations. All the patients will undergo B cell phenotyping, TCR repertoire, molecular signature from operational tolerance and a skin biopsy with immunohistochemical staining of the specimens in order to show signs of acute or chronic rejection.

The results could provide a valid tool to detect operationally tolerant recipients as well as recipients prone to develop chronic rejection.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Blood sample, biopsy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Search Tolerance Signature in Vascularised Composite Allograft
Study Start Date :
Oct 1, 2013
Actual Primary Completion Date :
Jul 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Outcome Measures

Primary Outcome Measures

  1. Biomarkers of molecular signature from operational tolerance and/or chronic rejection research [1 day]

    B cell phenotyping, TCR repertoire, molecular signature from operational tolerance

Secondary Outcome Measures

  1. Pathological characteristics of skin acute/chronic rejection on skin biopsy [1 day]

    skin biopsy with immunohistochemical staining of the specimens in order to show signs of acute or chronic rejection. We will try to correlate the signature of tolerance with the absence of chronic rejection symptoms, both clinically and in skin protocol biopsies.

  2. Phenotype of skin T lymphocyte in cutaneous biopsies [1 day]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient with Hand (unilateral/bilateral) or face allotransplantation for at least one year

  • Patient without clinical sign of acute rejection at inclusion

  • Patient who signed the informed protocol consent

  • Patient older than 18 years old

  • Patient covered by an health insurance

  • Patient without legal protection

Exclusion Criteria:
  • Patient with Hand or face allotransplantation for less than one year

  • Patient with clinical sign of acute rejection at inclusion

  • Unsigned protocol consent

  • Patient under the age of 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospices Civils de Lyon Lyon France 69003

Sponsors and Collaborators

  • Hospices Civils de Lyon
  • ISTITUTO ITALIANO CHIRURGIA DELLA MANO, Italy
  • medizinische universität innsbruck, Austria
  • Hospital Clínico Universitario de Valencia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT02055521
Other Study ID Numbers:
  • 2013.815
First Posted:
Feb 5, 2014
Last Update Posted:
Jul 18, 2014
Last Verified:
Jul 1, 2014

Study Results

No Results Posted as of Jul 18, 2014