Clinical relevance of low levels of preformed alloantibodies detected by flow cytometry in the first year post-kidney transplantation

Transplant Proc. 2005 Jul-Aug;37(6):2750-2. doi: 10.1016/j.transproceed.2005.05.040.

Abstract

Objective: To determine the prevalence of transplants performed with a false-negative cytotoxicity cross-match and to analyze the clinical relevance of alloantibodies (Ab) detected only by flow cytometry (flow).

Methods: We studied 66 patients undergoing kidney transplantation from a cadaveric donor. All patients had a simultaneous negative T+AHG+DTT and B+DTT. Pretransplant sera were retrospectively analyzed by flow cytometry according to an Emory University protocol: (1) T+ and B-: Ab anti-class I; (2) T- and B+: anti-class II; (3) T+B+: anti-class I + II. Chi-square, Fisher exact, Student t test, and Kaplan Meier analyses were employed with significance assigned at P < or = .05.

Results: The overall incidence of false-negative cytotoxicity was 33.3% (22/66), namely, 6.1% (n = 4) anti-class I; 9.1% (n = 6) anti-class II; and 18.2% (n = 12) anti-class I + II. Primary nonfunctioning grafts occurred in 6.8% (3/44) and 13.6% (3/22) negative and positive flow patients (two anti-class I + II and one class II; P = .39). The incidence of graft loss in the first year was respectively, 13.6% (6/44) and 18.2% (4/22; two anti-class II and two anti-class I + II; P = .72). Compared to flow-negative grafts, creatinine levels were significantly higher among flow-positive patients at 8 and 12 weeks. One-year graft survivals were 86.4% among negative versus 81.8% for the positive group (P = .67).

Conclusions: We observed that 33% of kidney transplant recipients had low levels of alloantibodies detected only by flow. This single factor was associated with the worst graft function in the first trimester with a suggestion of a higher risk for non-functioning graft.

MeSH terms

  • Cadaver
  • Cytotoxicity, Immunologic
  • False Negative Reactions
  • Flow Cytometry
  • Follow-Up Studies
  • Graft Rejection / epidemiology
  • Graft Survival / immunology
  • HLA-D Antigens / immunology
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Isoantibodies / blood*
  • Kidney Transplantation / immunology*
  • Kidney Transplantation / mortality
  • Survival Analysis
  • Tissue Donors
  • Treatment Outcome

Substances

  • HLA-D Antigens
  • Histocompatibility Antigens Class I
  • Isoantibodies