Pre- and post-transplant monitoring of soluble CD30 levels as predictor of acute renal allograft rejection

Transpl Immunol. 2007 Jun;17(4):278-82. doi: 10.1016/j.trim.2007.02.001. Epub 2007 Mar 13.

Abstract

Identification of renal graft candidates at high risk of impending acute rejection (AR) and graft loss may be helpful for patient-tailored immunosuppressive regimens and renal graft survival. To investigate the feasibility with soluble CD30 (sCD30) as predictor of AR, sCD30 levels of 70 patients were detected on day 0 pre-transplant and day 1, 3, 5, 7, 10, 14, 21, and 30 post-transplant. AR episodes in 6 months were recorded and then patients were divided into Group AR (n=11) and Group UC (n=59). Results showed that the patients had higher pre-transplant sCD30 levels than healthy people. A significant decrease of sCD30 was observed on the first day post-transplant and continued until day 14 post-transplant. Soluble CD30 presented a stable level from day 14 to 30 post-transplant. Pre-transplant sCD30 levels of Group AR were much higher than those of Group UC (P<0.001). Patients of Group AR also had higher sCD30 levels than those of Group UC on day 1, 3, 5, 7, 10 and 14 (P<0.001). The sCD30 level presented a significantly delayed decrease in the patients of Group AR. Statistical results showed that the highest value of area under ROC curve (0.95) was obtained on day 5 post-transplant, suggesting that sCD30 levels on day 5 are of high predictive value. Therefore, sCD30 level may be a good marker of increased alloreactivity and of significant predictive value. It's necessary to monitor the variation of sCD30 in the early period post-transplant.

MeSH terms

  • Adult
  • Cohort Studies
  • Female
  • Graft Rejection / diagnosis*
  • Humans
  • Immunosuppression Therapy
  • Ki-1 Antigen / blood*
  • Kidney Transplantation*
  • Male
  • Middle Aged
  • Monitoring, Immunologic*
  • Prognosis
  • Retrospective Studies

Substances

  • Ki-1 Antigen