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Selective intra-graft apoptosis and down-regulation of lymphocyte bcl-2, iNOs and CD95L expression in kidney-pancreas transplanted patients after anti-Thymoglobulin induction

Authors :
Giacomo Dell'Antonio
Silvano Rossini
Paolo Fiorina
Marta Bruno Ventre
Elena Orsenigo
Chiara Gremizzi
Valerio Di Carlo
Alberto M. Davalli
Gabriele Torriani
Antonio Secchi
Fiorina, P
Torriani, G
Gremizzi, C
Davalli, A
Orsenigo, E
BRUNO VENTRE, M
DELL ANTONIO, G
DI CARLO, V
Rossini, S
Secchi, Antonio
Source :
Transplant International. 17:603-608
Publication Year :
2004
Publisher :
Frontiers Media SA, 2004.

Abstract

Intra-graft infiltrating cells apoptosis was evaluated in 20 consecutive kidney-pancreas transplanted (KP) patients without kidney rejection. Two fine-needle aspirated biopsy (FNAB) and two peripheral blood lymphocytes (PBL) samples were obtained 14 days after transplantation. Immunosuppression was based on anti-Thymoglobulins (ATG) induction for 7 days and cyclosporine/mofetil mycophenolate as maintenance therapy. Ten matched healthy subjects were chosen as controls for PBL. Lymphocyte phenotypes and activation markers, apoptotic rate and lymphocyte expression of pro/anti-apoptotic molecules were analysed by flow cytometry analysis (FACS). Lymphocyte phenotypes and activation markers: higher levels of CD8 and CD4DR were evident in the graft (p0.05) than in PBL, CD3CD25 in PBL were higher in transplanted patients than in controls. Apoptotic rate and lymphocyte expression of pro- and anti-apoptotic molecules: a higher expression of annexin V, together with reduced lymphocytes CD95L, iNOs and Bcl-2 expression (PBL = 97.7+/-1.1% vs FNAB = 81.9+/-15.1%; p0.05) were evident in the graft than in PBL. In KP patients intra-graft apoptosis and reduced anti-apoptotic molecules were evident after ATG induction.

Details

ISSN :
14322277 and 09340874
Volume :
17
Database :
OpenAIRE
Journal :
Transplant International
Accession number :
edsair.doi.dedup.....91ff7cff9925207c0dab1d8127a4dff9
Full Text :
https://doi.org/10.1111/j.1432-2277.2004.tb00393.x