Human beta-herpesvirus interactions in solid organ transplant recipients

J Infect Dis. 2001 Jan 15;183(2):179-184. doi: 10.1086/317929. Epub 2000 Dec 15.

Abstract

The replication of beta-herpesviruses-cytomegalovirus (CMV), human herpesvirus (HHV)-6, and HHV-7-and their association with CMV disease and response to antiviral therapy were prospectively investigated in 33 liver transplant recipients not given antiviral prophylaxis. CMV, HHV-6, and HHV-7 DNA were detected within 8 weeks after transplantation in 70%, 33%, and 42% of the patients, respectively. The univariate association between CMV disease and the 3 beta-herpesviruses was more significant by virus load quantitation than by qualitative detection of DNA. This association with high levels of CMV, HHV-6, and HHV-7 (P<.001,.022, and.001, respectively) occurred mainly in CMV-seronegative recipients of transplants from CMV-seropositive donors. Antiviral therapy with ganciclovir (Gcv) reduced the load of CMV and HHV-6 and HHV-7. These results suggest that CMV disease in transplant recipients is related to the unique interaction of the 3 beta-herpesviruses and is ultimately reduced after intravenous Gcv treatment.

MeSH terms

  • Antibodies, Viral / blood
  • Antiviral Agents / therapeutic use
  • Cohort Studies
  • Cytomegalovirus / genetics
  • Cytomegalovirus / isolation & purification
  • Cytomegalovirus / physiology*
  • Cytomegalovirus Infections / drug therapy
  • Cytomegalovirus Infections / epidemiology
  • Cytomegalovirus Infections / virology*
  • DNA, Viral / blood
  • Ganciclovir / therapeutic use
  • Herpesvirus 6, Human / genetics
  • Herpesvirus 6, Human / isolation & purification
  • Herpesvirus 6, Human / physiology*
  • Herpesvirus 7, Human / genetics
  • Herpesvirus 7, Human / isolation & purification
  • Herpesvirus 7, Human / physiology*
  • Humans
  • Liver Transplantation / adverse effects*
  • Polymerase Chain Reaction
  • Virus Replication

Substances

  • Antibodies, Viral
  • Antiviral Agents
  • DNA, Viral
  • Ganciclovir