학술논문

Cytomegalovirus (CMV) infections and CMV-specific cellular immune reconstitution following reduced intensity conditioning allogeneic stem cell transplantation with Alemtuzumab.
Document Type
Article
Source
Bone Marrow Transplantation. Nov2005, Vol. 36 Issue 9, p797-802. 6p. 2 Charts, 2 Graphs.
Subject
*CYTOMEGALOVIRUS diseases
*IMMUNE response
*IMMUNOSPECIFICITY
*CELLULAR immunity
*IMMUNE recognition
*HOMOGRAFTS
*STEM cell transplantation
Language
ISSN
0268-3369
Abstract
Summary:We studied the incidence and recurrence of Cytomegalovirus (CMV) infection and reactivation in 38 recipients of Alemtuzumab reduced intensity conditioning-stem cell transplantation, and used CMV-HLA tetramer studies to discover if these events correlated with recovery of circulating CMV-specific CD8+ T cells (cytotoxic T lymphocyte (CTLs)). The cumulative incidence of CMV infection was 60% at 1 year (95% CI, 45–78%) with a median reactivation time of 24 days (range 5–95 days). All patients with CMV reactivation received Ganciclovir or Foscarnet, and only one developed CMV disease. More strikingly, only 8/21 patients had relapse of CMV antigenemia. Tetramer analysis in 13 patients showed that 11 reconstituted CMV CTLs (7/11 by day 30 and 10/11 by day 90). The development of CMV infection was accompanied by a >5-fold rise of CMV CTLs. Recurrence of CMV infection occurred only in the patients who failed to generate a CTL response to the virus. Hence, recipients of SCT using Alemtuzumab-RIC are initially profoundly immunosuppressed and have a high incidence of early CMV reactivation. However, in the majority of patients, infection is transient, and antiviral T cell reconstitution is rapid. Monitoring with CMV-specific CTLs may help identify the subset of patients at risk from recurrent infection or disease.Bone Marrow Transplantation (2005) 36, 797–802. doi:10.1038/sj.bmt.1705121; published online 5 September 2005 [ABSTRACT FROM AUTHOR]