NK Cell Transcripts and NK Cells in Kidney Biopsies from Patients with Donor-Specific Antibodies: Evidence for NK Cell Involvement in Antibody-Mediated Rejection

被引:321
|
作者
Hidalgo, L. G. [2 ]
Sis, B. [2 ]
Sellares, J. [1 ]
Campbell, P. M. [1 ,2 ]
Mengel, M. [2 ]
Einecke, G. [3 ]
Chang, J. [1 ]
Halloran, P. F. [1 ]
机构
[1] Univ Alberta, Dept Med, Div Nephrol & Transplant Immunol, Edmonton, AB, Canada
[2] Univ Alberta, Dept Lab Med & Pathol, Div Nephrol & Transplant Immunol, Edmonton, AB, Canada
[3] Hannover Med Sch, D-30623 Hannover, Germany
关键词
Antibody-mediated rejection; donor-specific antibody; HLA antibody; microarray; NK cell; renal allograft pathology; RENAL-ALLOGRAFT REJECTION; NATURAL-KILLER-CELLS; TRANSPLANT GLOMERULOPATHY; CYTOTOXIC LYMPHOCYTES; PATHOLOGICAL FEATURES; GRAFT LOSS; EXPRESSION; RECEPTOR; C4D; CLASSIFICATION;
D O I
10.1111/j.1600-6143.2010.03201.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
To explore the mechanisms of antibody-mediated rejection (ABMR) in kidney transplants, we studied the transcripts expressed in clinically indicated biopsies from patients with donor-specific antibody (DSA). Comparison of biopsies from DSA-positive versus DSA-negative patients revealed 132 differentially expressed transcripts: all were associated with class II DSA but none with class I DSA. Many transcripts were expressed in DSA-positive ABMR but were also expressed in T-cell-mediated rejection (TCMR), reflecting shared molecular features. Removal of shared transcripts created 23 DSA selective transcripts (DSASTs). Some DSASTs (6/23) showed selective high expression in NK cells, whereas others (8/23) were expressed in endothelium or in endothelium plus other cell types (7/23). Of 145 biopsies ranked by DSAST expression, the 25 with highest DSAST expression primarily consisted of ABMR (22/25, 88%), either C4d-positive or C4d-negative. By immunostaining, CD56+ and CD68+ cells in peritubular capillaries, but not CD3+ cells, were increased in ABMR compared to TCMR, compatible with a role for NK cells, as well as macrophages, as effectors in endothelial injury during ABMR. Thus, the strategy of using DSASTs in the biopsy to identify mechanism-related transcripts in biopsies from patients with clinical phenotypes indicates the selective involvement of NK cells in ABMR.
引用
收藏
页码:1812 / 1822
页数:11
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