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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.
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页码:1812 / 1822
页数:11
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