Literature DB >> 12581329

Increased expression of cytotoxic effector molecules: different interpretations for steroid-based and steroid-free immunosuppression.

Thomas Satterwhite1, Mei-Sze Chua, Szu-Chuan Hsieh, Stella Chang, John Scandling, Oscar Salvatierra, Minnie M Sarwal.   

Abstract

Cytotoxic T lymphocyte (CTL) effector molecules have been studied as markers of acute rejection in renal allograft recipients on steroid-based immunosuppression. We hypothesized that basal CTL gene expression may vary with time post-transplantation as well as with different immunosuppression protocols (steroid-based or steroid-free). Variations in CTL gene expression may thus impact on the ability to predict acute allograft rejection. We used the non-invasive method of quantitative competitive-reverse transcription-polymerase chain reaction (QC-RT-PCR) to quantify the amounts of CTL effector molecules (granulysin, GL; perforin, P; granzyme B, GB) in serial peripheral blood lymphocyte (PBL) samples from steroid-free and steroid-based adult and pediatric renal allograft recipients. Patients on both protocols were clinically monitored by protocol biopsies at 1, 3, 6, and 12 months post-transplantation and for graft function at 1 yr post-transplantation in a separate clinical study. Steroid-free patients with stable graft function showed an increase in GL, P, and GB gene expression over time post-transplantation with the increase being seen largely by the first post-transplant month. A further increase in GL expression was noted at the end of the first post-transplant year in the absence of acute rejection, whereas GB and P levels were unchanged. At comparative time-points post-transplantation, CTL genes were found to be higher in steroid-free patients with stable graft function, compared to steroid-based recipients with either clinically stable graft function or acute rejection. This study suggests that levels of CTL gene expression, although important in a steroid-based regimen to monitor the risk of acute rejection, may not be similarly applied in patients on steroid-free immunosuppression. The early increase in levels seen in steroid-free patients appears to correlate with the total absence of steroids. As steroid-free patients seem to have a lower incidence of acute rejection and better long-term graft function at 1 yr, the early increase in CTL genes in the absence of acute rejection may suggest an early adaptive immune activation response, promoting early graft acceptance in this protocol.

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Year:  2003        PMID: 12581329     DOI: 10.1034/j.1399-3046.2003.02053.x

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  8 in total

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Review 4.  Corticosteroid avoidance in pediatric renal transplantation: can it be achieved?

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5.  Steroid-free immunosuppression since 1999: 129 pediatric renal transplants with sustained graft and patient benefits.

Authors:  L Li; A Chang; M Naesens; N Kambham; J Waskerwitz; J Martin; C Wong; S Alexander; P Grimm; W Concepcion; O Salvatierra; M M Sarwal
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6.  Evaluation of vascular lesions using circulating endothelial cells in renal transplant patients.

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Review 7.  Steroids in kidney transplant patients.

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8.  Requirement of cognate CD4+ T-cell recognition for the regulation of allospecific CTL by human CD4+ CD127- CD25+ FOXP3+ cells generated in MLR.

Authors:  Yuming Yu; Joshua Miller; Joseph R Leventhal; Anat R Tambur; Dhivya Chandrasekaran; Josh Levitsky; Xunrong Luo; James M Mathew
Journal:  PLoS One       Date:  2011-07-22       Impact factor: 3.240

  8 in total

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