Biology of Blood and Marrow Transplantation
Volume 9, Issue 9 , Pages 543-558, September 2003

Cytomegalovirus in hematopoietic stem cell transplant recipients: current status, known challenges, and future strategies

  • Michael Boeckh

      Affiliations

    • Fred Hutchinson Cancer Research Center and the University of Washington, Seattle, Washington, USA
    • Corresponding Author InformationCorrespondence and reprint requests: Michael Boeckh, MD, Program in Infectious Diseases, Fred Hutchinson Cancer Research Center, P.O. Box 19024, Seattle, WA 8109–1024, USA
  • ,
  • W.Garrett Nichols

      Affiliations

    • Fred Hutchinson Cancer Research Center and the University of Washington, Seattle, Washington, USA
  • ,
  • Genovefa Papanicolaou

      Affiliations

    • Memorial Sloan-Kettering Cancer Center, New York, New York, USA
  • ,
  • Robert Rubin

      Affiliations

    • Harvard Medical School, Brigham and Women’s Hospital and Harvard/Massachusetts Institute of Technology, Division of Health Sciences and Technology, Boston, Massachusetts, USA
  • ,
  • John R Wingard

      Affiliations

    • University of Florida College of Medicine, Gainesville, Florida, USA
  • ,
  • John Zaia

      Affiliations

    • City of Hope National Medical Center and Beckman Research Institute, Duarte, California, USA

Received 17 July 2003; accepted 1 August 2003.

Abstract 

Cytomegalovirus (CMV) infection is a major cause of morbidity and mortality after hematopoietic stem cell transplantation. Significant progress has been made in the prevention of CMV disease over the past decade, but prevention of late CMV disease continues to be a challenge in selected high-risk populations. The pretransplantation CMV serostatus of the donor and/or recipient remains an important risk factor for posttransplantation outcome despite the use of antiviral prophylaxis and preemptive therapy; CMV-seropositive recipients of T cell-depleted grafts in particular continue to have a survival disadvantage compared with seronegative recipients with seronegative donors. The risk of developing antiviral drug resistance remains low in most patients; however, in a setting of intense immunosuppression (eg, after transplantation from a haploidentical donor), the incidence may be as high as 8%. Primary CMV infection via blood transfusion can be reduced by the provision of seronegative or leukocyte-depleted blood products; however, a small risk of 1% to 2% of CMV disease remains. Surveillance and preemptive therapy are effective in preventing the sequelae of transfusion-related CMV infection. Indirect immunomodulatory effects of CMV are increasingly recognized in hematopoietic stem cell transplant recipients. Strategies currently being investigated include long-term suppression of CMV with valganciclovir for the prevention of late CMV infection and disease, adoptive transfer of CMV-specific T cells, and donor and recipient vaccination strategies.

Keywords:  CMV, Herpes virus, Hematopoietic stem cell, Transplantation, Immunosuppression, Resistance

 

PII: S1083-8791(03)00287-8

doi:10.1016/S1083-8791(03)00287-8

Biology of Blood and Marrow Transplantation
Volume 9, Issue 9 , Pages 543-558, September 2003