ELISA-based detection of C4d after liver transplantation--a helpful tool for differential diagnosis between acute rejection and HCV-recurrence?

Transpl Immunol. 2010 Aug;23(4):156-60. doi: 10.1016/j.trim.2010.06.002. Epub 2010 Jun 14.

Abstract

Hepatitis-C is the most common indication for liver transplantation. Recurrence of HCV is universal leading to graft failure in up to 40% of all patients. The differentiation between acute rejection and recurrent hepatitis-C is crucial as rejection treatments are likely to aggravate HCV-recurrence. Histological examination of liver biopsy remains the gold standard for diagnosis of acute rejection but has failed in the past to distinguish between acute rejection and recurrent hepatitis-C. In a retrospective study we have recently reported that C4d as a marker of the activated complement cascade is detectable in a hepatic specimen in acute rejection after liver transplantation and may serve as a valuable tool in differential diagnosis between ACR and HCV-recurrence. We performed a prospective analysis by ELISA measurement of C4d concentration in cryo-preserved liver biopsies of LTX patients who had either experienced acute rejection, hepatitis-C recurrence or displayed no pathological alterations (controls). Opposed to our immunohistologically based findings in paraffinized tissue we were unable to detect significant differences of C4d concentration in ELISA of cryo-preserved liver tissue. Consequently the role and potential value of C4d as a diagnostic marker may not be determined using ELISA-based tissue evaluation.

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Biomarkers / metabolism
  • Complement C4b / immunology
  • Complement C4b / metabolism
  • Diagnosis, Differential
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Graft Rejection / diagnosis*
  • Graft Rejection / immunology
  • Graft Rejection / pathology
  • Graft Rejection / physiopathology
  • Hepacivirus / immunology*
  • Hepacivirus / pathogenicity
  • Hepatitis C / diagnosis*
  • Hepatitis C / immunology
  • Hepatitis C / pathology
  • Hepatitis C / physiopathology
  • Humans
  • Liver / immunology
  • Liver / metabolism*
  • Liver / pathology
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Recurrence
  • Retrospective Studies

Substances

  • Biomarkers
  • Peptide Fragments
  • Complement C4b
  • complement C4d