Cytomegalovirus in hematopoietic stem cell transplant recipients - management of infection

Expert Rev Hematol. 2016 Nov;9(11):1093-1105. doi: 10.1080/17474086.2016.1242406. Epub 2016 Oct 11.

Abstract

Cytomegalovirus (CMV) still causes significant morbidity and mortality in patients given allogeneic hematopoietic stem cell transplantation (HSCT). Despite effective pharmacotherapy, potentially life-threatening CMV disease occurs nowadays in up to 10% of HSCT recipients; moreover, routinely used anti-CMV agents have been shown to be associated with morbidity. Areas covered: This review examines different issues related to diagnosis and management of CMV infection in HSCT recipients, paying particular attention to the monitoring of CMV-specific immune recovery, approaches of adoptive cell therapy and new antiviral drugs. Expert commentary: Despite advances in diagnostic tests and treatment, there is still room for refining management of CMV in HSCT recipients. Immunological monitoring should be associated in the future to virological monitoring. The safety profile and efficacy of new anti-CMV agents should be compared with that of standard-of-care drugs. Donor-derived, pathogen-specific T cells adoptively transferred after transplantation could contribute to reduce the impact of CMV infection on patient's outcome.

Keywords: CMV infection; CMV vaccines; adoptive T-cell therapy; anti-viral drugs; generation of CMV-specific T cells; immune monitoring; monitoring of CMV viral load.

Publication types

  • Review

MeSH terms

  • Antiviral Agents / therapeutic use
  • Blood Component Transfusion / adverse effects
  • Cytomegalovirus Infections / diagnosis
  • Cytomegalovirus Infections / etiology*
  • Cytomegalovirus Infections / prevention & control
  • Cytomegalovirus Infections / therapy
  • Cytomegalovirus Vaccines / administration & dosage
  • Cytomegalovirus Vaccines / immunology
  • Cytomegalovirus* / immunology
  • Cytomegalovirus* / physiology
  • Drug Resistance, Viral
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Immunity, Innate
  • Immunotherapy, Adoptive
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Tissue Donors
  • Transplant Recipients
  • Virus Activation / immunology
  • Virus Replication

Substances

  • Antiviral Agents
  • Cytomegalovirus Vaccines