The role of positive flow cytometry crossmatch in late renal allograft loss

Hum Immunol. 2009 Jul;70(7):502-5. doi: 10.1016/j.humimm.2009.04.002. Epub 2009 Apr 11.

Abstract

Many studies relating flow cytometery crossmatch (FCXM) results to kidney transplant outcomes have examined risk in the first 3 to 12 months. We used Organ Procurement and Transplant Network registry data for 66,594 kidney transplants from 1995 to 2007 to investigate associations of T-cell positive (T+) and T-cell negative/B-cell positive (T(-)B+) FCXM with graft failure risk early (years 0-1) and late (years >1-5) after transplant. Compared with transplants with T-cell negative/B-cell negative (T(-)B(-)) FCXM, living-donor transplants performed after T+ FCXM had significantly higher adjusted, relative risks of both early (adjusted hazards ratio [aHR] 1.71, p < 0.0001) and late (aHR 1.36, p = 0.017) graft loss. T(-)B+ FCXM was associated with approximately 40% higher relative risk of graft loss in the late period only. Patterns were similar for deceased-donor transplants. The risks of positive FCXM persist beyond the peritransplant period for years after transplant. Damage by memory effector cells may explain the long-term risks associated with positive FCXM.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • B-Lymphocytes / immunology
  • Cytotoxicity, Immunologic
  • Flow Cytometry / methods*
  • Graft Rejection / immunology*
  • Graft Survival / immunology
  • Histocompatibility Testing / methods*
  • Humans
  • Kaplan-Meier Estimate
  • Kidney Transplantation / immunology*
  • Kidney Transplantation / methods
  • Registries / statistics & numerical data
  • T-Lymphocytes / immunology
  • Tissue and Organ Procurement / organization & administration
  • Tissue and Organ Procurement / statistics & numerical data
  • Transplantation, Homologous