Functional analysis of cytomegalovirus-specific T lymphocytes compared to tetramer assay in patients undergoing hematopoietic stem cell transplantation

Bone Marrow Transplant. 2008 Mar;41(6):515-21. doi: 10.1038/sj.bmt.1705932. Epub 2007 Nov 19.

Abstract

In order to evaluate whether we could predict reactivation of CMV by monitoring the number of CMV-specific cytotoxic T-lymphocytes (CTL), tetramer analysis was performed in 37 patients who underwent hematopoietic stem cell transplantation (HSCT). The results disclosed that the mean number of CMV-specific CTL at day 30 did not differ among patients who developed CMV antigenemia (22/microl) and those who did not (12/microl). Serial tetramer analysis showed that 21% of the patients had >10/microl CMV-specific CTL at the first detection of CMV antigenemia and 67% of the patients had more than 10/microl CMV-specific CTL at the onset of CMV disease. Intracellular staining upon stimulation by CMV lysates and peptide in patients with CMV colitis revealed that both IFN-gamma producing CD4+ and CD8+ lymphocytes were suppressed at the onset of CMV colitis (1.6 and 8/microl), which increased with recovery of the disease (19 and 47/microl). These data suggest that it is difficult to predict CMV reactivation solely by the number of CMV-specific CTL. We suggest that additional functional analysis by intracellular cytokine assay may be useful for immunomonitoring against CMV.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Antigens, Viral / blood
  • Antigens, Viral / metabolism
  • Colitis / virology
  • Cytomegalovirus / immunology*
  • Cytomegalovirus / physiology
  • Cytomegalovirus Infections / diagnosis
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / prevention & control
  • Epitopes, T-Lymphocyte / immunology
  • HLA-A Antigens / metabolism
  • HLA-A2 Antigen
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Humans
  • Interferon-gamma / metabolism
  • Lymphocyte Count / methods
  • Middle Aged
  • Phosphoproteins
  • Risk Factors
  • T-Lymphocytes, Cytotoxic / immunology*
  • Time Factors
  • Viral Matrix Proteins
  • Virus Activation

Substances

  • Antigens, Viral
  • Epitopes, T-Lymphocyte
  • HLA-A Antigens
  • HLA-A*02 antigen
  • HLA-A2 Antigen
  • Phosphoproteins
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa
  • Interferon-gamma