Comparison of two dosages of thymoglobulin used as a short-course for induction in kidney transplantation

Détails

ID Serval
serval:BIB_98206189844A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Comparison of two dosages of thymoglobulin used as a short-course for induction in kidney transplantation
Périodique
Transplant International
Auteur⸱e⸱s
Wong  W., Agrawal  N., Pascual  M., Anderson  D. C., Hirsch  H. H., Fujimoto  K., Cardarelli  F., Winkelmayer  W. C., Cosimi  A. B., Tolkoff-Rubin  N.
ISSN
0934-0874
Statut éditorial
Publié
Date de publication
08/2006
Peer-reviewed
Oui
Volume
19
Numéro
8
Pages
629-35
Notes
Clinical Trial
Comparative Study
Journal Article --- Old month value: Aug
Résumé
Thymoglobulin is used effectively as an induction agent in kidney transplantation, but the optimal dose is not well established. We evaluated the degree and durability of T-cell clearances with two different thymoglobulin regimens in adult kidney transplant recipients (KTR). Seven KTR received a 3-day thymoglobulin-based induction of 1.0 mg/kg/day while nine received 1.5 mg/kg/day, in addition to maintenance immunosuppression. Lymphocyte subsets were monitored for 6 months. Renal function, infections and malignancies were monitored for 24 months. T-cell subsets were significantly lower by day 30 with the thymoglobulin 1.5 mg/kg/day regimen when compared with the 1.0 mg/kg/day regimen; this trend was sustained at 6-month (CD3(+): 438 +/- 254 vs. 1001 +/- 532 cells/mm(3), P = 0.016). Renal function between the two groups was not significantly different at 6- and 24-months post-transplant. One case of BK Virus viremia in the 1.5 mg/kg/day thymoglobulin group was detected. No acute rejection episodes, cytomegalovirus infections, or malignancies were noted in either group. Thymoglobulin induction was efficacious in both groups, but with a significantly sustained T-cell clearance in the 1.5 mg/kg/day regimen. A more profound T-cell clearance within the first 6 months postinduction therapy may translate into a decreased risk of immunological injury and improved long-term outcome after kidney transplantation.
Mots-clé
Aged Antibodies, Monoclonal/*administration & dosage/adverse effects Dose-Response Relationship, Immunologic Female Humans Immunosuppression/adverse effects/methods *Kidney Transplantation/immunology Lymphocyte Count Lymphocyte Depletion Male Middle Aged T-Lymphocyte Subsets/immunology Time Factors
Pubmed
Web of science
Open Access
Oui
Création de la notice
29/01/2008 14:52
Dernière modification de la notice
20/08/2019 15:59
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