The immunosuppressive effect of human cytomegalovirus infection in recipients of allogeneic hematopoietic stem cell transplantation

  • S. Giebel
  • , R. Maccario
  • , D. Lilleri
  • , M. Zecca
  • , M. A. Avanzini
  • , M. Marconi
  • , A. Di Cesare Merlone
  • , G. Campanini
  • , D. Montagna
  • , P. Travaglino
  • , R. Gentile
  • , Rocco Gentile
  • , S. Telli
  • , D. Pagliara
  • , J. Holowiecki
  • , Franco Locatelli

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

In immune-competent individuals, human cytomegalovirus ( HCMV) infection is associated with impairment of T-cell function. Our goal was to evaluate prospectively whether clinically asymptomatic HCMV infection in allogeneic hematopoietic stem cell transplantation (alloHSCT) recipients, treated pre emptively with ganciclovir, influences T-cell function as well. Mitogen-stimulated T-cell proliferative activity, together with cell surface markers, was tested in 49 patients on days +30, +45, +60, and +90 after alloHSCT and, additionally, in cases of positive HCMV pp65-antigenemia. HCMV infection was diagnosed in 19 patients. None of them developed HCMV disease. T-cell proliferative activity was significantly decreased on days when HCMV antigenemia was positive as compared to days without antigenemia. The number of pp65-positive cells negatively correlated with proliferative response. Comparison of patients who did experience HCMV infection with those who did not reveals significant decrease of T-cell proliferative activity observed on days +30 and +45, a time period when antigenemia was most frequently found to be positive, whereas no difference was detected on days +60 and +90. We conclude that, even clinically asymptomatic, HCMV infection has negative impact on T-cell proliferation capacity in alloHSCT recipients. However, pre emptive therapy with ganciclovir makes this immunosuppressive effect transient and restricted to the time of infection duration.
Lingua originaleInglese
pagine (da-a)503-509
Numero di pagine3
RivistaBone Marrow Transplantation
Volume36
DOI
Stato di pubblicazionePubblicato - 2005

Keywords

  • HCMV
  • T cells
  • alloHSCT

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