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Molecular profiling of acute and chronic rejections of renal allografts
H. Petra, H. Eva, B. Irena, H. Petra, V. Ondřej,
Language English Country Egypt
Document type Journal Article, Research Support, Non-U.S. Gov't
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PubMed
24302958
DOI
10.1155/2013/509259
Knihovny.cz E-resources
- MeSH
- Allografts immunology metabolism MeSH
- Biopsy MeSH
- Adult MeSH
- Patient Outcome Assessment MeSH
- Kidney immunology metabolism pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Prognosis MeSH
- Gene Expression Regulation MeSH
- Graft Rejection genetics immunology mortality MeSH
- Risk Factors MeSH
- ROC Curve MeSH
- Cluster Analysis MeSH
- Gene Expression Profiling * MeSH
- Transcriptome MeSH
- Kidney Transplantation adverse effects MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Both antibody mediated (AMR) and T-cell mediated (TCMR) rejections either acute or chronic represent the main reason for late graft dysfunction. In this study we aimed to evaluate differences in the intrarenal expression patterns of immune system related genes in acute and chronic rejections. Graft biopsies were performed and evaluated according to Banff classification. Using the TaqMan Low Density Array, the intrarenal expressions of 376 genes relating to immune response (B-cell activation, T-cell activation, chemokines, growth factors, immune regulators, and apoptosis) were analyzed in the four rejection categories: chronic AMR, chronic TCMR, acute AMR, and acute TCMR. The set of genes significantly upregulated in acute TCMR as compared to acute AMR was identified, while no difference in gene expressions between chronic rejections groups was found. In comparison with functioning grafts, grafts that failed within the next 24 months after the chronic rejection morphological confirmation presented at biopsy already established severe graft injury (low eGFR, higher proteinuria), longer followup, higher expression of CDC20, CXCL6, DIABLO, GABRP, KIAA0101, ME2, MMP7, NFATC4, and TGFB3 mRNA, and lower expression of CCL19 and TRADD mRNA. In conclusion, both Banff 2007 chronic rejection categories did not differ in intrarenal expression of 376 selected genes associated with immune response.
References provided by Crossref.org
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