Kidney injury molecule-1 expression in transplant biopsies is a sensitive measure of cell injury

被引:151
作者
Zhang, P. L. [2 ,3 ]
Rothblum, L. I. [3 ]
Han, W. K. [1 ]
Blasick, T. M. [3 ]
Potdar, S. [4 ]
Bonventre, J. V. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
[2] Geisinger Med Ctr, Div Lab Med, Danville, PA 17822 USA
[3] Geisinger Med Ctr, Weis Ctr Res, Danville, PA 17822 USA
[4] Geisinger Med Ctr, Dept Transplantat, Danville, PA 17822 USA
关键词
D O I
10.1038/sj.ki.5002697
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
Kidney injury molecule-1 (KIM-1) is a specific histological biomarker for diagnosing early tubular injury on renal biopsies. In this study, KIM-1 expression was quantitated in renal transplant biopsies by immunohistochemistry and correlated with renal function. None of the 25 protocol biopsies showed detectable tubular injury on histologic examination, yet 28% had focal positive KIM-1 expression. Proximal tubule KIM-1 expression was present in all biopsies from patients with histological changes showing acute tubular damage and deterioration of kidney function. In this group, higher KIM-1 staining predicted a better outcome with improved blood urea nitrogen ( BUN), serum creatinine, and estimated glomerular filtration rate (eGFR) over an ensuing 18 months. KIM-1 was expressed focally in affected tubules in 92% of kidney biopsies from patients with acute cellular rejection. By contrast, there was little positive staining for Ki-67, a cell proliferation marker, in any of the groups. KIM-1 expression significantly correlated with serum creatinine and BUN, and inversely with the eGFR on the biopsy day. Our study shows that KIM-1 staining sensitively and specifically identified proximal tubular injury and correlated with the degree of renal dysfunction. KIM-1 expression is more sensitive than histology for detecting early tubular injury, and its level of expression in transplant biopsies may indicate the potential for recovery of kidney function.
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收藏
页码:608 / 614
页数:7
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