Long-term results of CMV hyperimmune globulin prophylaxis in 377 heart transplant recipients

J Heart Lung Transplant. 2003 Mar;22(3):250-7. doi: 10.1016/s1053-2498(02)00474-6.

Abstract

Background: Cytomegalovirus (CMV) has emerged as the most important pathogen to affect the post-operative course after heart transplantation. We performed a retrospective analysis to evaluate the efficiency of CMV hyperimmune globulin (CMVIG) prophylaxis in preventing CMV disease in aggressively immunosuppressed patients after heart transplantation.

Methods: We studied 377 heart transplant recipients who received quadruple-immunosuppressive therapy and CMVIG as sole CMV prophylaxis. The study population was categorized into 4 groups according to donor and recipient CMV serology at the time of transplantation (D+/R+, D+/R-, D-/R+, D-/R-) and was monitored for CMV immediate early antigen in peripheral blood cells, in urine sediments, and in throat washings; for the presence of serum CMV immunoglobulin M and CMV immunoglobulin G; and for clinical evidence of CMV-related symptoms. In addition, we compared the incidence of cardiac allograft vasculopathy and infection among the groups.

Results: During the first 5 years after transplantation, CMV disease developed in 79 patients (20.96%). Comparison among the groups showed significantly increased risk for CMV disease in allograft recipients of organs from seropositive donors (D+, 27.31%; D-, 11.33%; p = 0.0003). We observed 6 CMV-associated deaths, all in CMV-antibody-negative recipients. Additionally CMV-positive recipients had a greater incidence of cardiac allograft vasculopathy (p = 0.048), and a greater overall infection rate (p = 0.0034).

Conclusions: Cytomegalovirus hyperimmune globulin administration prevents CMV disease and infection in aggressively immunosuppressed heart transplant recipients. Because fatal CMV disease in CMV-negative recipients of organs from seropositive donors could not be prevented with CMVIG alone, we recommend the additional use of prophylactic ganciclovir in this CMV-mismatched population.

MeSH terms

  • Antiviral Agents / therapeutic use
  • Cytomegalovirus Infections / drug therapy
  • Cytomegalovirus Infections / prevention & control*
  • Female
  • Follow-Up Studies
  • Ganciclovir / therapeutic use
  • Heart Transplantation*
  • Humans
  • Immunization, Passive*
  • Immunoglobulins / administration & dosage*
  • Immunoglobulins, Intravenous
  • Immunosuppression Therapy
  • Immunosuppressive Agents / therapeutic use
  • Male
  • Middle Aged
  • Retrospective Studies
  • Time Factors
  • Transplantation, Homologous

Substances

  • Antiviral Agents
  • Immunoglobulins
  • Immunoglobulins, Intravenous
  • Immunosuppressive Agents
  • cytomegalovirus-specific hyperimmune globulin
  • Ganciclovir