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

被引:32
作者
Satterwhite, T [1 ]
Chua, MS [1 ]
Hsieh, SC [1 ]
Chang, S [1 ]
Scandling, J [1 ]
Salvatierra, O [1 ]
Sarwal, MM [1 ]
机构
[1] Stanford Univ, Dept Pediat, Sch Med, CCSR, Stanford, CA 94305 USA
关键词
renal transplant; cytotoxic effector molecules; immunosuppression; corticosteroids; steroid-free; RT-PCR;
D O I
10.1034/j.1399-3046.2003.02053.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:53 / 58
页数:6
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