| Literature DB >> 22172091 |
Uluhan Sili1, Ann M Leen, Juan F Vera, Adrian P Gee, Helen Huls, Helen E Heslop, Catherine M Bollard, Cliona M Rooney.
Abstract
Infections with a range of common community viruses remain a major cause of mortality and morbidity after allogeneic hematopoietic stem cell transplantation. T cells specific for cytomegalovirus (CMV), Epstein-Barr virus (EBV) and adenoviruses can safely prevent and infections with these three most common culprits, but the manufacture of individual T cell lines for each virus would be prohibitive in terms of time and cost. We have demonstrated that T cells specific for all three viruses can be manufactured in a single culture using monocytes and EBV-transformed B lymphoblastoid cell lines (LCLs), both transduced with an adenovirus vector expressing pp65 of CMV, as antigen-presenting cells. Trivirus-specific T cell lines produced from healthy stem cell donors could prevent and treat infections with all three viruses, not only in the designated recipient, but in unrelated, partially-HLA-matched third party recipients. We now provide the details and logistics of T cell manufacture.Entities:
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Year: 2012 PMID: 22172091 PMCID: PMC3705934 DOI: 10.3109/14653249.2011.636963
Source DB: PubMed Journal: Cytotherapy ISSN: 1465-3249 Impact factor: 5.414