Expression of cyclooxygenase-1 and cyclooxygenase-2 in human renal allograft rejection-- a prospective study

Transpl Int. 2006 Mar;19(3):203-12. doi: 10.1111/j.1432-2277.2005.00261.x.

Abstract

Cyclooxygenases (COX) are known to be involved in inflammatory kidney diseases. However, there are no data available about the expression of COX-1 and only preliminary reports about the expression of COX-2 in biopsies of patients undergoing acute renal allograft rejection. We conducted this prospective study to analyze the expression, distribution, and cellular localization of COX-1 and -2 and thus to elucidate the role of COX in human kidney transplantation. One hundred forty-four biopsies were included from patients without rejection and unaltered morphology (n = 60), with acute interstitial rejection (n = 7), with acute vascular rejection (n = 21), with chronic allograft nephropathy (n = 16), without rejection but with various other lesions (n = 40). COX-1 and -2 expression was localized in each biopsy by immunohistochemistry. We found a highly significant up-regulation of COX-1 in vessels and in infiltrating interstitial cells of patients with acute allograft rejection compared with biopsies with well-preserved tissue. Also, COX-2 expression was significantly elevated in infiltrating interstitial cells of biopsies with acute rejection. This is the first prospective study demonstrating a significant induction of both COX-1 and -2 in human allograft biopsies with acute rejection after renal transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Arteriosclerosis / pathology
  • Biopsy
  • Cyclooxygenase 1 / biosynthesis*
  • Cyclooxygenase 2 / biosynthesis*
  • Female
  • Gene Expression
  • Gene Expression Regulation, Enzymologic
  • Graft Rejection
  • Humans
  • Immunohistochemistry
  • Kidney / enzymology*
  • Kidney Transplantation*
  • Male
  • Middle Aged
  • Prospective Studies
  • Time Factors
  • Treatment Outcome
  • Up-Regulation

Substances

  • Cyclooxygenase 1
  • Cyclooxygenase 2