Molecular comparison of calcineurin inhibitor-induced fibrogenic responses in protocol renal transplant biopsies

被引:54
作者
Groningen, Marian C. Roos-van
Scholten, Eduard M.
Lelieveld, Patrick M.
Rowshani, Ajda T.
Baelde, Hans J.
Bajema, Ingeborg M.
Florquin, Sandrine
Bemelman, Frederike J.
de Heer, Emile
de Fijter, Johan W.
Bruijn, Jan A.
Eikmans, Michael
机构
[1] Leiden Univ, Med Ctr, Dept Pathol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Nephrol, NL-2300 RC Leiden, Netherlands
[3] Acad Med Ctr, Renal Transplant Unit, Dept Internal Med, Amsterdam, Netherlands
[4] Acad Med Ctr, Dept Pathol, Amsterdam, Netherlands
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2006年 / 17卷 / 03期
关键词
D O I
10.1681/ASN.2005080891
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The calcineurin inhibitor cyclosporine (CsA) induces a fibrogenic response that may lead to scarring of the renal allograft. This study investigated whether tacrolimus, a novel calcineurin inhibitor, exerts fibrogenic effects to a similar extent. Sixty patients were enrolled in a randomized study: 29 received CsA, and 31 received tacrolimus. Patients were subjected to tailored exposure-controlled calcineurin inhibitor regimens. Protocol biopsies were obtained at the time of transplantation and 6 and 12 mo after transplantation. Cortical TGF-beta and collagens alpha 1(I) and alpha 1(III) mRNA steady-state levels were determined with real-time PCR. The extent of protein deposition of TGF-beta, alpha-smooth muscle actin, and interstitial collagens in the renal cortex was quantified with computer-assisted image analysis. The extent of interstitial collagen deposition measured with Sirius red and the accumulation of alpha-smooth muscle actin and TGF-beta protein after 6 and 12 mo were similar for both immunosuppressive regimens. mRNA levels of TGF-beta and collagens alpha 1(I) and alpha 1(III) were not significantly different in the treatment groups either. It is concluded that the fibrogenic response in renal allografts is similar in patients who receive CsA-based regimens and patients who receive tacrolimus-based regimens.
引用
收藏
页码:881 / 888
页数:8
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