In vitro T cell proliferation from kidney allograft biopsies with unremarkable pathology: new strategies for an old problem

Transplantation. 2002 Jan 15;73(1):142-5. doi: 10.1097/00007890-200201150-00026.

Abstract

Acute rejection of renal allografts is mediated by infiltrating alloreactive T cells. The goals of this study were to correlate T cell proliferation with rejection and to determine whether T cell proliferation in the absence of rejection would predict future rejection episodes. Toward this, kidney biopsies (n=100) were cultured in the presence of interleukin-2. Cultures were examined at 4, 24, and 48 hr for T cell proliferation. A strong correlation was observed between T cell proliferation at any time point and rejection. There was not a significant correlation between T cell proliferation in biopsies with no rejection and the occurrence of a rejection episode within 2 months. However, T cell proliferation after 4 hr was a better predictor of the occurrence of rejection within 2 months compared with observations after 24 and 48 hr. Therefore, a subgroup of patients with unremarkable biopsies but T cell proliferation may be at risk for rejection and warrant closer observation and possible tailoring of immunosuppression.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Biopsy, Needle
  • Graft Rejection / immunology
  • Graft Rejection / pathology
  • Humans
  • Kidney Transplantation / immunology*
  • Kidney Transplantation / pathology
  • Lymphocyte Activation*
  • Predictive Value of Tests
  • Retrospective Studies
  • T-Lymphocytes / immunology*
  • Transplantation, Homologous