The involvement of activated T cells and growth-factor production in the early and late phase of chronic kidney allograft nephropathy in rats

P. Hamar, Attila Szabó, V. Müller, Uwe Heemann

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

T cells are thought to play a regulatory role in chronic allograft nephropathy (CAN). Thus, we investigated whether lymphocyte inhibition influences CAN. Fisher rat (F-344) kidneys were transplanted orthotopically into Lewis rats. Animals received cyclosporin A (1.5 mg/kg per day, s.c.) for 10 days and were treated daily with either cyclosporin A (1.5 mg/kg), tacrolimus (0.16 mg/kg), or a vehicle thereafter (n = 15 per group). Kidneys were harvested at 16 or 24 weeks. Interleukin-2 (IL-2) and interleukin-2 receptor β (IL-2Rβ) mRNA synthesis were intense at 16 weeks and decreased thereafter. Unsurprisingly, both cyclosporin A and tacrolimus significantly inhibited IL-2 and IL-2Rβ at both time points. Proteinuria increased more rapidly in controls than in treated animals. Morphologically, over 40% of glomeruli were sclerosed by 16 weeks in controls, and ED-1+ macrophages and CD5+ T cells infiltrated the graft. IL-2 mRNA synthesis paralleled the number of infiltrating cells. Inhibition of T-cell proliferation significantly reduced glomerulosclerosis and leukocyte infiltration at both time points. Transforming growth factor (TGF)-β1 and platelet-derived growth factor (PDGF) synthesis were highly upregulated in controls at 16 weeks, the time of peak infiltration. At 24 weeks, as cellular infiltration was replaced by scar formation, TGF-β1 mRNA returned to normal, while PDGF did not. Inhibition of T cells prevented the upregulation of TGF-β1 at both time points; however, PDGF was suppressed only at week 16. These results indicate a beneficial effect of continuous suppression of T cells in CAN. T cells are probably more important in the early, inflammatory phase.

Original languageEnglish
Pages (from-to)446-454
Number of pages9
JournalTransplant International
Volume15
Issue number9-10
DOIs
Publication statusPublished - 2002

Fingerprint

Interleukin-2
Allografts
T-Lymphocytes
Kidney
Platelet-Derived Growth Factor
Transforming Growth Factors
Cyclosporine
Interleukin-2 Receptors
Tacrolimus
Messenger RNA
Proteinuria
Cicatrix
Leukocytes
Up-Regulation
Cell Count
Macrophages
Cell Proliferation
Lymphocytes
Transplants

Keywords

  • Chronic allograft nephropathy
  • Interleukin-2
  • Platelet-derived growth factor
  • T cells
  • Transforming growth factor-β

ASJC Scopus subject areas

  • Transplantation

Cite this

The involvement of activated T cells and growth-factor production in the early and late phase of chronic kidney allograft nephropathy in rats. / Hamar, P.; Szabó, Attila; Müller, V.; Heemann, Uwe.

In: Transplant International, Vol. 15, No. 9-10, 2002, p. 446-454.

Research output: Contribution to journalArticle

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