| Literature DB >> 26863474 |
Geurt Stokman1, Jesper Kers, Ünsal Yapici, Joris J Hoelbeek, Nike Claessen, Onno J de Boer, Mihai G Netea, Luuk Hilbrands, Fréderike J Bemelman, Ineke J M Ten Berge, Sandrine Florquin.
Abstract
Polyomavirus-associated nephropathy (PVAN) occurs in a significant percentage of renal transplant recipients, with BK virus reactivation as the main causative agent. PVAN leads to tubular damage and may result in allograft loss. In this study, we analyzed the antiviral immune response in PVAN. Transcription of the proinflammatory cytokine interleukin-18 (IL-18) was significantly higher in PVAN biopsies compared with T cell-mediated rejection (TCMR) (1.42 ± 0.20 and 0.69 ± 0.10, respectively; *P = 0.0021). Tubular expression of IL-18 was significantly increased in PVAN compared with TCMR (2.00 ± 0.24 and 1.333 ± 0.13, respectively; *P = 0.028). In contrast, in TCMR, IL-18 was expressed predominantly by CD163-positive macrophages. These data suggest that the antiviral immune response in PVAN is partly coordinated by the tubular epithelium, whereas in TCMR, this may be controlled by inflammatory cells.Entities:
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Year: 2016 PMID: 26863474 DOI: 10.1097/TP.0000000000001086
Source DB: PubMed Journal: Transplantation ISSN: 0041-1337 Impact factor: 4.939