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Updated: Jun 16, 2026

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Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Bortezomib as the sole post-renal transplantation desensitization agent does not decrease donor-specific anti-HLA
R Sberro-Soussan1, J Zuber, C Suberbielle-Boissel
1Université Paris Descartes, Paris, France.
Summary
One cycle of bortezomib alone did not reduce donor-specific anti-HLA antibodies (DSA) in kidney transplant recipients with antibody-mediated rejection. Further studies are needed to assess bortezomib
Area of Science:
- Nephrology
- Immunology
- Transplantation
Background:
- Donor-specific anti-HLA antibodies (DSA) persistence post-kidney transplant is linked to antibody-mediated rejection and poor graft survival.
- Targeting plasma cells with proteasome inhibitors like bortezomib is a potential desensitization strategy.
Observation:
- This study assessed bortezomib's efficacy as a sole desensitization therapy in four kidney transplant recipients with subacute antibody-mediated rejection and high DSA levels.
- Bortezomib treatment involved one cycle of four doses (1.3 mg/m(2) each).
Findings:
- Bortezomib did not significantly decrease DSA levels within 150 days post-treatment in any patient.
- Antivirus antibody levels (HBV, VZV, HSV) remained stable, indicating no significant impact on long-lived plasma cells.
Implications:
- One cycle of bortezomib monotherapy is insufficient to lower DSA in sensitized kidney transplant recipients within the observed timeframe.
- Rigorous, prospective, randomized, and controlled studies are essential to properly evaluate bortezomib's role in desensitization strategies.
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