Autologous peripheral blood progenitor cells are a potential source of parvovirus B19 infection

TitleAutologous peripheral blood progenitor cells are a potential source of parvovirus B19 infection
Publication TypeJournal Article
Year of Publication2005
AuthorsArnold DM, Neame PB, Meyer RM, Soamboonsrup P, Luinstra KE, O'Hoski P, Garner J, Foley R
JournalTransfusion
Volume45
Issue3
Pagination394 - 8
Date PublishedMar
Type of ArticleCase Reports Research Support, Non-U.S. Gov't
ISSN0041-1132 (Print) 0041-1132 (Linking)
Accession Number15752157
KeywordsDNA, Viral / analysis, Female, Hematopoietic Stem Cell Transplantation / *adverse effects, Hematopoietic Stem Cells / *virology, Humans, Lymphoma, B-Cell / therapy, Lymphoma, Large B-Cell, Diffuse / *therapy, Middle Aged, Parvoviridae Infections / *etiology / transmission, Parvovirus B19, Human / genetics / *isolation & purification
Abstract

BACKGROUND: Parvovirus B19 is a cause of delayed red blood cell (RBC) engraftment after marrow transplantation (BMT). The diagnosis of parvovirus infection requires serologic and DNA testing in the context of clinical disease and characteristic marrow morphologic findings; however, the source of infection is often difficult to determine. STUDY DESIGN AND METHODS: Investigation of a case of delayed RBC engraftment and pure RBC aplasia (PRCA) occurring 3 months after autologous peripheral blood progenitor cell (PBPC) transplantation in a patient with high-risk diffuse large B-cell lymphoma. DNA testing of serum and of a sample of cryopreserved PBPCs was performed. RESULTS: Marrow morphology showed a maturational arrest of erythroid cells with giant proerythroblasts. Polymerase chain reaction and nucleic acid hybridization confirmed the presence of parvovirus DNA in the serum and in a sample of sequestered PBPCs saved at the time of PBPC harvest. PRCA resolved after the administration of intravenous immune globulin. CONCLUSION: Autologous PBPCs are a potential source of parvovirus infection, which may cause significant disease after autologous BMT.

DOI10.1111/j.1537-2995.2005.04267.x
Alternate JournalTransfusion
Notify Library Reference ID94

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