Cytomegalovirus (CMV)-specific cellular immune responses

Hum Immunol. 2004 May;65(5):500-6. doi: 10.1016/j.humimm.2004.02.012.

Abstract

A large percentage of healthy individuals (50-90%) is chronically infected with Cytomegalovirus (CMV). Over the past few years, several techniques were developed in order to monitor CMV-specific T-cell responses. In addition to the identification of antigen-specific T cells with peptide-loaded MHC complexes, most of the current strategies to identify CMV-specific T cells are centered on the assessment of the functions of memory T cells including their ability to mediate effector function, to proliferate or to secrete cytokines following antigen-specific stimulation. The investigation of these functions has allowed the characterization of the CMV-specific T-cell responses that are present during different phases of the infection. Furthermore, it has also been shown that the combination of virus-specific CD4 and CD8 T-cell responses are critical components of the immune response in the control of virus replication.

Publication types

  • Review

MeSH terms

  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / immunology
  • Cytomegalovirus / immunology*
  • Cytomegalovirus Infections / immunology*
  • Flow Cytometry / methods
  • HIV-1 / immunology
  • Histocompatibility Antigens Class I / analysis
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Immunity, Cellular / immunology*
  • Immunologic Surveillance / immunology
  • Interferon-gamma / metabolism
  • Monitoring, Immunologic / methods
  • Phosphoproteins / immunology
  • Receptors, CCR7
  • Receptors, Chemokine / analysis
  • Transplantation / adverse effects
  • Viral Matrix Proteins / immunology

Substances

  • CCR7 protein, human
  • Histocompatibility Antigens Class I
  • Phosphoproteins
  • Receptors, CCR7
  • Receptors, Chemokine
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa
  • Interferon-gamma