Development of drug-resistant herpes simplex virus infection after haploidentical hematopoietic progenitor cell transplantation

Author:

Langston Amelia A.1,Redei Istvan1,Caliendo Angela M.1,Somani Jyoti1,Hutcherson Don1,Lonial Sagar1,Bucur Silvana1,Cherry Judy1,Allen Andrew1,Waller Edmund K.1

Affiliation:

1. From the Emory University School of Medicine, Winship Cancer Institute, Department of Hematology-Oncology, Bone Marrow and Stem Cell Transplant Center, and Departments of Pathology and Infectious Diseases, Emory University, Atlanta, Georgia.

Abstract

Abstract An unusually high incidence of acyclovir- and foscarnet-resistant herpes simplex virus (HSV) infection was noted after lymphocyte-depleted blood hematopoietic progenitor cell (HPC) transplantation from HLA-haploidentical family donors. Fourteen adults with hematologic malignancies underwent blood HPC transplantation from haploidentical family donors. Pheresis products were stringently depleted of T and B cells by immunomagnetic adsorption, and patients received no immunosuppression after transplantation. HSV reactivation occurred in all 7 evaluable HSV-1– or HSV-2–seropositive patients, at a median of 40 days after transplantation. Susceptibility testing of clinically resistant viral isolates demonstrated acyclovir resistance in all 5 cases tested. Second-line therapy produced only partial responses, and in vitro evidence of foscarnet resistance developed rapidly in all 3 patients treated with foscarnet. Healing of lesions coincided with T-cell recovery. The prolonged immunodeficiency associated with stringent lymphocyte depletion of the graft appears to strongly predispose to emergence of drug-resistant HSV. Furthermore, immune reconstitution is necessary for eradication of infection.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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