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Effect of immunosuppressive regimen on acute rejection and liver graft function

Authors :
Ziolkowski, J.
Paczek, L.
Niewczas, M.
Senatorski, G.
Oldakowska-Jedynak, U.
Wyzgal, J.
Foroncewicz, B.
Mucha, K.
Zegarska, J.
Nyckowski, P.
Zieniewicz, K.
Patkowski, W.
Krawczyk, M.
Ziarkiewicz-Wroblewska, B.
Gornicka, B.
Source :
Transplantation Proceedings. Sep2003, Vol. 35 Issue 6, p2281. 3p.
Publication Year :
2003

Abstract

Despite the use of modern immunosuppressive drugs, acute liver rejection (AR) continues to affect up to 70% of transplant recipients. The aim of this retrospective study was to assess the incidence of acute rejection episodes in patients treated with different immunosuppressive protocols. In our series, 37.3% of patients developed a clinical episode of AR. Analysis of immunosuppression has shown that the most effective immunosuppressive protocols, with regard to prevention of AR, include: antibody anti–IL-2R (anti–IL-2R) + tacrolimus (Tac) + mycophenolate mofetil (MMF) + prednisolone (Pred); anti–IL-2R + tacrolimus (Tac) + Pred; or Tac + Pred (25% vs 28.6% vs 30.4%, respectively). The highest rate of AR (66.6%) was observed among patients with anti–IL-2R and Tac but no steroid treatment, mostly (77.7%) in the initial period after liver transplantation. There were no statistical differences in liver function tests between the group treated with a CsA-based versus a Tac-based therapy. Strong immunosuppression contributed to a relatively low incidence of clinical AR in our series. The lowest rate of AR was observed among patients treated with anti–IL-2R antibody. Tac, and Pred. Deprivation of steroids in the early phase after liver transplantation substantially increased the risk of acute rejection episodes despite the use of anti–CD25. There were no statistically significant differences in liver function tests among those treated with Tac versus CsA in the short-term follow-up. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00411345
Volume :
35
Issue :
6
Database :
Academic Search Index
Journal :
Transplantation Proceedings
Publication Type :
Academic Journal
Accession number :
10926771
Full Text :
https://doi.org/10.1016/S0041-1345(03)00794-2