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Efficacy and safety of BORTEZOMIB treatment for refractory acute antibody-mediated rejection-a pilot study
J. Slatinska, A. Slavcev, E. Honsova, P. Hruba, I. Kratochvilova, T. Rohal, O. Viklicky,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30168284
DOI
10.1111/tan.13387
Knihovny.cz E-zdroje
- MeSH
- bezpečnost pacientů MeSH
- bortezomib terapeutické užití MeSH
- dárci tkání MeSH
- dospělí MeSH
- HLA antigeny genetika imunologie MeSH
- homologní transplantace MeSH
- hormony kůry nadledvin terapeutické užití MeSH
- imunologické faktory terapeutické užití MeSH
- isoprotilátky krev MeSH
- lidé středního věku MeSH
- lidé MeSH
- pilotní projekty MeSH
- plazmaferéza metody MeSH
- přežívání štěpu * MeSH
- prognóza MeSH
- rejekce štěpu krev diagnóza imunologie patologie MeSH
- rituximab terapeutické užití MeSH
- rozvrh dávkování léků MeSH
- testování histokompatibility metody MeSH
- transplantace ledvin * MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
A novel therapeutic approach to refractory acute antibody-mediated rejection (AMR) in kidney transplant recipients was applied in 23 patients based on administration of Bortezomib, intravenous corticosteroids, plasmapheresis and Rituximab. Application of Bortezomib regimen led to diminishing of donor-specific antibodies (DSA) to HLA-B (P = 0.004) and HLA-DR (P = 0.0005), but not to HLA-A (P = 0.106) and HLA-DQ antigens (P = 0.18). Patients with good clinical response to treatment had significantly better allograft survival than recipients with continuing deterioration of graft function (P = 0.019). Graft survival after therapy of refractory AMR was significantly worse than survival after first transplantation and was comparable with outcomes after retransplantation. In conclusion, therapy with Bortezomib was well tolerated and effective in decreasing the levels of HLA-B and -DR antibodies, however, was not successful in depleting HLA-A and -DQ DSA.
Department of Immunogenetics Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Nephrology Institute for Clinical and Experimental Medicine Prague Czech Republic
Transplant Laboratory Institute for Clinical and Experimental Medicine Prague Czech Republic
Citace poskytuje Crossref.org
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