Intracellular IFNgamma production in CD3 negative cells exposed to allo-antigens is an indicator of prior sensitization

Transpl Immunol. 2010 Feb;22(3-4):121-7. doi: 10.1016/j.trim.2009.11.004. Epub 2009 Nov 26.

Abstract

Background: Sensitization to HLA antigens (Ags) is a significant obstacle to kidney transplantation and risk factor for antibody-mediated rejection (AMR). Current screening methods to assess HLA Ag exposure include various antibody assays. However, tools to accurately measure cell-mediated immunity to allo-Ags in a clinical setting are lacking. Here we report on an intracellular cytokine flow cytometry (CFC) assay that detects intracellular gamma-interferon (IFNgamma) production in non-T cell populations (CD3-) that appears to assess sensitization from previous allo-Ag exposure.

Methods: Blood from 106 highly-HLA sensitized (HS) patients (pre-, post-IVIG-treatment [Rx] and/or post-transplant) and 14 3(rd) party normal controls (3(rd)N) were incubated with donor or 3(rd)N peripheral blood mononuclear cells (PBMCs), and IFNgamma+/CD3- cells were enumerated.

Results: The percentage of IFNgamma+ cells in CD3- cells without stimulation in pre-IVIG-Rx HS patients was similar to normals, but significantly increased with incubation with donor and/or 3(rd)N PBMCs. Reactivity in normals was minimal. Reactivity was higher in HS females than HS males. Normal females with previous pregnancy (PG) showed significantly higher response than females without PG or non-sensitized normal males. Donor-specific reactivity in the CFC assay better correlated with donor-specific B cell crossmatch than total anti-HLA antibody levels or PRA. HS patients who developed AMR post-transplant showed significantly higher reactivity than those without AMR.

Conclusions: The CFC assay measures IFNgamma production in CD3- cells that may indicate a memory response to allo-Ags. This response is limited to HS patients and normal females with previous PG. Patients undergoing AMR show significantly higher reactivity. This assay may represent a novel approach to measurement of allo-sensitization with clinical utility in predicting those at risk for AMR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • CD3 Complex / biosynthesis
  • Cell Count
  • Child
  • Female
  • Flow Cytometry / methods
  • Graft Rejection / diagnosis
  • Graft Rejection / epidemiology
  • Graft Rejection / immunology*
  • HLA Antigens / immunology*
  • Humans
  • Immunization*
  • Immunologic Memory
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism*
  • Kidney Transplantation
  • Male
  • Middle Aged
  • Pregnancy
  • Risk Factors
  • Sex Factors*

Substances

  • CD3 Complex
  • HLA Antigens
  • Interferon-gamma