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Blood, 15 June 2002, Vol. 99, No. 12, pp. 4357-4363
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
High incidence of cytomegalovirus infection after
nonmyeloablative stem cell transplantation: potential role of
Campath-1H in delaying immune reconstitution
Suparno Chakrabarti,
Stephen Mackinnon,
Raj Chopra,
Panagiotis D. Kottaridis,
Karl Peggs,
Peter O'Gorman,
Ronjon Chakraverty,
Timothy Marshall,
Husam Osman,
Premini Mahendra,
Charles Craddock,
Herman Waldmann,
Geoff Hale,
Christopher D. Fegan,
Kwee Yong,
Anthony H. Goldstone,
David C. Linch, and
Donald W. Milligan
From the Departments of Haematology and Public Health
Laboratories, Birmingham Heartlands Hospital, Department of Public
Health and Epidemiology, Institute of Cancer Studies, University of
Birmingham, Birmingham, United Kingdom; Department of Haematology,
University College Hospital, London, United Kingdom; Department of
Haematology, Christie Hospital, Manchester University Hospital,
Birmingham, United Kingdom; and Sir William Dunn School of Pathology,
Oxford, United Kingdom.
Nonmyeloablative conditioning is increasingly used for
transplantation in a wide range of diseases, but little is known about its impact on the incidence of infections and immune reconstitution. We
examined the pattern and outcome of cytomegalovirus (CMV) infections monitored by polymerase chain reaction-based assays and treated preemptively in 101 patients following nonmyeloablative conditioning containing in vivo Campath-1H. Fifty-one patients (50%) had a CMV
infection at a median of 27 days after transplantation with a
probability of 84.8% in patients at risk of CMV infection. The probability of recurrence of CMV infection before and after 100 days
was 53.6% and 46.6%, respectively, and was more common in unrelated
donor transplant recipients. All 3 patients who developed CMV disease
died of this complication. The 2 patients with late CMV disease had
grade III to IV graft-versus-host-disease (GVHD), which occurred de
novo in only 4% of patients and in another 10% following donor
lymphocyte infusions. The median time to CD4+ T-cell count
more than 200/µL was 9 months in the 48 patients studied. The
probabilities of overall survival and nonrelapse mortality at 18 months
were 65% and 27.8%, respectively, with no significant difference in
survival between CMV-infected and -uninfected patients. The use of
Campath-1H appeared to be associated with a low incidence of GVHD but a
high incidence of CMV infections and prolonged immune paresis.

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Related Letter in Blood Online:
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CMV infection following nonmyeloablative allogeneic stem cell transplantation using Campath
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Blood 2002 100: 3843.
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