Sources and sequelae of bacterial contamination of hematopoietic stem cell components: implications for the safety of hematotherapy and graft engineering

TitleSources and sequelae of bacterial contamination of hematopoietic stem cell components: implications for the safety of hematotherapy and graft engineering
Publication TypeJournal Article
Year of Publication1996
AuthorsWebb IJ, Coral FS, Andersen JW, Elias AD, Finberg RW, Nadler LM, Ritz J, Anderson KC
JournalTransfusion
Volume36
Issue9
Pagination782 - 8
Date PublishedSep
Type of ArticleResearch Support, U.S. Gov't, P.H.S.
ISSN0041-1132 (Print) 0041-1132 (Linking)
Accession Number8823450
KeywordsAntibodies, Monoclonal / therapeutic use, Antigens, CD34 / analysis, Bacterial Infections / *transmission, Bone Marrow Cells, Bone Marrow Purging, Freezing, Hematopoietic Stem Cell Transplantation / *standards, Humans, Lymphocyte Depletion
Abstract

BACKGROUND: It is important to compare the incidence of bacterial contamination of components collected from the peripheral blood or bone marrow (BM), as well as of components processed with or without cell selection or depletion, and to evaluate the sequelae of such contamination. STUDY DESIGN AND METHODS: Bacterial contamination rates were compared in 1380 untreated autologous peripheral blood progenitor cells (PBPCs), 291 untreated autologous BM samples, 916 monoclonal antibody (MoAb)-treated autologous and allogeneic BM samples, and in 45 autologous PBPC components from which the CD34+ cells were selected. Bacterial cultures were performed at sequential time points during the processing of MoAb-treated BM. RESULTS: Bacterial contamination was documented in 44 of 2632 components from 1593 patients (1.67% of components, 2.76% of patients) before cryopreservation. Although only 0.65% of untreated PBPCs were contaminated before cryopreservation, each patient was more likely to have given a contaminated PBPC component than a contaminated BM component (2.41% vs. 0%, p

Alternate JournalTransfusion
Notify Library Reference ID1612

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