Inconsistent responses of cytomegalovirus-specific T cells to pp65 and IE-1 versus infected dendritic cells in organ transplant recipients

Am J Transplant. 2007 Aug;7(8):1997-2005. doi: 10.1111/j.1600-6143.2007.01890.x.

Abstract

CD4(+) and CD8(+) T cells specific for human cytomegalovirus (HCMV) and two immunodominant HCMV antigens (pp65 and IE-1) were monitored in 20 solid organ transplant recipients undergoing primary (n = 4) or reactivated (n = 16) HCMV infection during the first year after transplantation by using as a stimulator either HCMV-infected autologous dendritic cells (DCs) or pp65- or IE-1 peptide mixtures. Turnaround times for test performance were 7 days for infected DCs and 24 h for peptides. Using infected DCs, HCMV-specific T-cell restoration occurred in all patients for CD8(+) and in 18/20 (90%) for CD4(+) T-cell subpopulations, resulting in virus clearance from blood. Using peptide mixtures, T-cell responses were less frequently detected. In detail, 14 (70%) patients showed pp65-specific CD8(+) T cells and 10 (50%) patients IE-1-specific CD8(+) T cells, whereas pp65-specific CD4(+) T cells were detected in 14 (70%) patients, and IE-1-specific CD4(+) T cells in three (15%) patients only. Protection from HCMV infection was associated with the presence of a HCMV-specific T-cell response directed against multiple viral proteins, but not against pp65 or IE-1 only. In conclusion, the use of pp65 and IE-1 peptide mixtures for rapid monitoring of HCMV-specific T-cell responses in solid organ transplant recipients underestimates the actual T-cell immune response against HCMV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Viral / immunology*
  • Cytomegalovirus / immunology*
  • Cytomegalovirus / isolation & purification
  • Cytomegalovirus Infections / immunology
  • Cytomegalovirus Infections / pathology
  • Cytomegalovirus Infections / virology
  • Dendritic Cells / immunology
  • Dendritic Cells / virology*
  • Flow Cytometry
  • Heart Transplantation / immunology
  • Heart Transplantation / pathology
  • Humans
  • Immediate-Early Proteins / immunology*
  • Kidney Transplantation / immunology
  • Kidney Transplantation / pathology
  • Organ Transplantation*
  • Phosphoproteins / immunology*
  • Prognosis
  • T-Lymphocytes / immunology
  • T-Lymphocytes / virology*
  • Trans-Activators / immunology*
  • Viral Matrix Proteins / immunology*

Substances

  • Antigens, Viral
  • IE-1 protein, murine cytomegalovirus
  • Immediate-Early Proteins
  • Phosphoproteins
  • Trans-Activators
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa