Identification of Non Invasive Biomarkers of Immune Endothelial Injury and Repair Associated With Cardiac Allograft Vasculopathy
Study Details
Study Description
Brief Summary
Heart transplantation is the best option for patients with end-stage heart failure. Cardiac allograft vasculopathy (CAV) is the leading cause of death following cardiac transplantation and is not managed by current therapies. Its pathogenesis traduces in an accelerated form of coronary artery disease (CAD) with similarities to atherosclerosis but also particular features of endothelial dysfunction associated to the alloimmune conflict and humoral responses toward the graft. Intravascular ultrasound (IVUS) is the validated invasive method for late CAV diagnosis, but occurs lesions are established. Identification of reliable non-invasive early endothelial injury biomarkers that reflect mechanisms of cardiac damage thus remain a major challenge to optimize therapeutic management of post transplant morbidity. Endothelial dysfunction is a central feature of both CAV and CAD and results from a desquilibrium in the balance of endothelial lesion and repair that is partly controlled by recipient immune system. Through their expression of receptors sensing antibodies (FcR CD16) and endothelial stress-induced signals (CX3CR1 fractalkine receptor and NKG2D MICA receptors), Natural Killer (NK) cells represent effector cells with unique potential to generate both humoral and innate immune injury of graft endothelium.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: HTC with Cardiac allograft vasculopathy HTC:heart transplanted recipients |
Biological: blood samples
|
| Other: HTR without Cardiac allograft vasculopathy
|
Biological: blood samples
|
| Other: untransplanted
|
Biological: blood samples
|
Outcome Measures
Primary Outcome Measures
- Analysis of endothelial lesion-repair biomarkers [24 MONTHS]
through phenotypic and quantitative analysis of circulating endothelial progenitors subsets and (repair potential)
Secondary Outcome Measures
- Analysis of anti endothelial NK innate immune responses parameters [24 MONTTHS]
Anti endothelial, anti HLA anti MIC antibody detection in recipient' serum by luminex and flow cytometry Evaluation of soluble Fractalkine and MIC levels in serum through ELISA Analysis of CX3CR1 and CD16 polymorphism and phenotypic NK cell surface expression Assay of serum induced and natural NK cell cytotoxicity against coronary and endothelial cell targets
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Subject > 18 years at the time of the inclusion,
-
Subject having benefited from a heart transplant more than 11 months ago in the service of cardiac surgery concerned whatever is the treatment to immunosuppresseur current
-
Subject benefiting from a coronarography within the framework of their surveillance comment-Clerk's Office beyond 12 months
-
Subject having given their consent
-
Affiliated to the Social Security
- HTC with Cardiac allograft vasculopathy:
- Subject with coronaropathies diagnosed by the coronarography
- TC without Cardiac allograft vasculopathy:
- Subject without coronaropathies diagnosed by the coronarography
- untransplanted
-
Untreated Subject by immunosuppresseurs
-
Subject without antécédaent of transfusion
-
Subject without history of transplantations
-
Subject with coronaropathies diagnosed by a coronarography
Exclusion Criteria:
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Presenting a contraindication to the coronarography
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Subject refusing to practise the examination of coronarography
-
Subject reaches(affects) of a cancer other one than cutaneous
-
Subject achieves of hepatic Incapacity (ALAT and\or ASAT > 3N)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Assistance Publique Hopitaux de Marseille | Marseille | France |
Sponsors and Collaborators
- Assistance Publique Hopitaux De Marseille
Investigators
- Study Director: BERNARD BELAIGUES, Assistance Publique hôpitaux de Marseille
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2010-A01145-34
- 2010 18