4.6 Article

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

期刊

AMERICAN JOURNAL OF TRANSPLANTATION
卷 10, 期 8, 页码 1812-1822

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1600-6143.2010.03201.x

关键词

Antibody-mediated rejection; donor-specific antibody; HLA antibody; microarray; NK cell; renal allograft pathology

资金

  1. Genome Canada
  2. Genome Alberta
  3. University of Alberta
  4. University of Alberta Hospital Foundation
  5. Roche Molecular Systems
  6. Hoffmann-La Roche Canada Ltd.
  7. Alberta Ministry of Advanced Education and Technology
  8. Roche Organ Transplantation Research Foundation
  9. Kidney Foundation of Canada
  10. Astellas Canada

向作者/读者索取更多资源

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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