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Risk factors for cytomegalovirus infection and disease in renal transplant recipients: HLA-DR7 and triple therapy.

Abstract
In a prospective study, an analysis of risk factors for the development of cytomegalovirus (CMV) infection and disease was performed on 77 renal allograft recipients. Twenty-five out of the 77 recipients (32%) had a CMV infection. Twenty-two of the recipients received triple immunosuppressive therapy (cyclosporin A, prednisolone, and azathioprine) while the remaining 55 received standard therapy (cyclosporin A and prednisolone). In 23 recipients (30%) acute rejection was diagnosed and the first positive parameter of infection occurred 22 days after rejection therapy. Infection occurred in 10 out of 18 HLA-DR7-positive recipients (56%) and in 15 out of 59 HLA-DR7-negative recipients (25%; P < 0.02). In multiple regression analysis, HLA-DR7 was found to be a significant predictor of CMV infection (P < 0.005). CMV disease was diagnosed in only 9 out of 25 recipients with an acute infection. Six recipients (67%) with CMV disease received triple therapy for maintenance immunosuppression; this was significantly correlated to CMV disease (P < 0.05) as compared to three recipients (33%) with CMV disease maintained with standard therapy. Our data suggest that HLA-DR7-positive recipients are more susceptible to CMV infection and that CMV disease is associated with triple immunosuppressive therapy.
AuthorsY J Kraat, M H Christiaans, F H Nieman, P M van den Berg-Loonen, J P van Hooff, C A Bruggeman
JournalTransplant international : official journal of the European Society for Organ Transplantation (Transpl Int) Vol. 7 Issue 5 Pg. 362-7 (Aug 1994) ISSN: 0934-0874 [Print] Switzerland
PMID7993574 (Publication Type: Journal Article)
Chemical References
  • HLA-DR7 Antigen
  • Immunosuppressive Agents
Topics
  • Acute Disease
  • Complement Fixation Tests
  • Cytomegalovirus (isolation & purification)
  • Cytomegalovirus Infections (diagnosis, etiology)
  • Enzyme-Linked Immunosorbent Assay
  • Graft Rejection (drug therapy)
  • HLA-DR7 Antigen (analysis)
  • Histocompatibility Testing
  • Humans
  • Immunosuppressive Agents (therapeutic use)
  • Kidney Transplantation (adverse effects, immunology)
  • Lymphocytes (virology)
  • Prospective Studies
  • Risk Factors
  • Transplantation, Homologous

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