Use of leflunomide in an allogeneic bone marrow transplant recipient with refractory cytomegalovirus infection

被引:67
作者
Avery, RK
Bolwell, BJ
Yen-Lieberman, B
Lurain, N
Waldman, WJ
Longworth, DL
Taege, AJ
Mossad, SB
Kohn, D
Long, JR
Curtis, J
Kalaycio, M
Pohlman, B
Williams, JW
机构
[1] Cleveland Clin Fdn, Dept Infect Dis, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Bone Marrow Transplantat Program, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Dept Clin Virol, Cleveland, OH 44195 USA
[4] Rush Med Coll, Dept Immunol Microbiol, Chicago, IL 60612 USA
[5] Ohio State Univ, Med Ctr, Dept Pathol, Columbus, OH 43210 USA
[6] Cleveland Clin Fdn, Dept Pharm, Cleveland, OH 44195 USA
[7] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
关键词
leflunomide; cytomegalovirus; antiviral resistance;
D O I
10.1038/sj.bmt.1704694
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Ganciclovir-resistant cytomegalovirus (CMV) infection is an emerging problem in transplant recipients. Foscarnet resistance and cidofovir resistance have also been described, but no previous reports have suggested treatment regimens for patients with CMV refractory to all three of these drugs. Leflunomide, an immunosuppressive drug used in rheumatoid arthritis and in rejection in solid-organ transplantation, has been reported to have novel anti-CMV activity. However, its clinical utility in CMV treatment has not been described previously. We report an allogeneic bone marrow transplant recipient who developed CMV infection refractory to sequential therapy with ganciclovir, foscarnet, and cidofovir. The patient was ultimately treated with a combination of leflunomide and foscarnet. Both phenotypic and genotypic virologic analysis was performed on sequential CMV isolates. The patient's high CMV-DNA viral load became undetectable on leflunomide and foscarnet, but the patient, who had severe graft-versus-host disease (GVHD) of the liver, expired with progressive liver failure and other complications. We concluded that leflunomide is a new immunosuppressive agent with anti-CMV activity, which may be useful in the treatment of multiresistant CMV. However, the toxicity profile of leflunomide in patients with underlying GVHD remains to be defined.
引用
收藏
页码:1071 / 1075
页数:5
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