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Expression of HLA-DR on T lymphocytes following renal transplantation, and association with graft-rejection episodes and cytomegalovirus infection

  • A. van Es
  • , W. M. Baldwin
  • , P. J. Oljans
  • , H. J. Tanke
  • , J. S. Ploem
  • , L. A. van Es

Research output: Contribution to journal › Article › peer-review

Abstract

The expression of HLA-DR by T lymphocyte subpopulations recognized by monoclonal antibodies and flow cytometry was monitored in 10 normal controls, 15 patients on hemodialysis, 25 recipients of a renal allograft with stable graft function, 16 transplant recipients suffering rejection episodes, and 4 transplant recipients with cytomegalovirus (CMV)4 infection. No significant differences in HLA-DR expression were observed in the OKT4-reactive subpopulation among these controls and patients. In the 16 patients who suffered rejection episodes a significant increase·in HLA-DR expression by OKT8-reactive cells was observed. In the 10 patients in whom rejection episodes occcurred later than 1 week after transplantation, the percentage of OKT8-reactive cells that expressed HLA-DR was dramatically increased 2–6 days before the onset of clinical symptoms of rejection (P <0.001 Student’s t test). When the rejection episode responded to treatment, expression of HLA-DR on the OKT8-reactive cells decreased―whereas in 3 patients who lost their grafts because of irreversible rejection, expression of HLA-DR remained elevated. In addition, the 4 patients with CMV infection had increased percentages of OKT8-reactive cells that expressed HLA-DR (P <0.001 Student’s t test). This increase in expression of HLA-DR coincided with the onset of clinical symptoms of the CMV infection, and the expression of HLA-DR returned to normal values after the titers of antibodies to CMV had increased significantly and symptoms of infection had disappeared.

Original languageEnglish (US)
Pages (from-to)65-69
Number of pages5
JournalTransplantation
Volume37
Issue number1
StatePublished - 1984
Externally publishedYes

ASJC Scopus subject areas

  • Transplantation
  • Immunology

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