Cargando…

Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood

Umbilical cord blood (CB) has emerged as an effective alternative donor source for hematopoietic stem cell transplantation. Despite this success, the prolonged duration of immune suppression following CB transplantation and the naiveté of CB T cells leave patients susceptible to viral infections. Ad...

Descripción completa

Detalles Bibliográficos
Autores principales: Dave, Hema, Luo, Min, Blaney, J.W., Patel, Shabnum, Barese, Cecilia, Cruz, Conrad Russell, Shpall, Elizabeth J., Bollard, Catherine M., Hanley, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415312/
https://www.ncbi.nlm.nih.gov/pubmed/28480300
http://dx.doi.org/10.1016/j.omtm.2017.02.001
_version_ 1783233499943141376
author Dave, Hema
Luo, Min
Blaney, J.W.
Patel, Shabnum
Barese, Cecilia
Cruz, Conrad Russell
Shpall, Elizabeth J.
Bollard, Catherine M.
Hanley, Patrick J.
author_facet Dave, Hema
Luo, Min
Blaney, J.W.
Patel, Shabnum
Barese, Cecilia
Cruz, Conrad Russell
Shpall, Elizabeth J.
Bollard, Catherine M.
Hanley, Patrick J.
author_sort Dave, Hema
collection PubMed
description Umbilical cord blood (CB) has emerged as an effective alternative donor source for hematopoietic stem cell transplantation. Despite this success, the prolonged duration of immune suppression following CB transplantation and the naiveté of CB T cells leave patients susceptible to viral infections. Adoptive transfer of ex vivo-expanded virus-specific T cells from CB is both feasible and safe. However, the manufacturing process of these cells is complicated, lengthy, and labor-intensive. We have now developed a simplified method to manufacture a single culture of polyclonal multivirus-specific cytotoxic T cells in less than 30 days. It eliminates the need for a live virus or transduction with a viral vector, thus making this approach widely available and GMP-applicable to target multiple viruses. The use of overlapping PepMixes as a source of antigen stimulation enable expansion of the repertoire of the T cell product to any virus of interest and make it available as a third party “off the shelf” treatment for viral infections following transplantation.
format Online
Article
Text
id pubmed-5415312
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-54153122017-05-05 Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood Dave, Hema Luo, Min Blaney, J.W. Patel, Shabnum Barese, Cecilia Cruz, Conrad Russell Shpall, Elizabeth J. Bollard, Catherine M. Hanley, Patrick J. Mol Ther Methods Clin Dev Original Article Umbilical cord blood (CB) has emerged as an effective alternative donor source for hematopoietic stem cell transplantation. Despite this success, the prolonged duration of immune suppression following CB transplantation and the naiveté of CB T cells leave patients susceptible to viral infections. Adoptive transfer of ex vivo-expanded virus-specific T cells from CB is both feasible and safe. However, the manufacturing process of these cells is complicated, lengthy, and labor-intensive. We have now developed a simplified method to manufacture a single culture of polyclonal multivirus-specific cytotoxic T cells in less than 30 days. It eliminates the need for a live virus or transduction with a viral vector, thus making this approach widely available and GMP-applicable to target multiple viruses. The use of overlapping PepMixes as a source of antigen stimulation enable expansion of the repertoire of the T cell product to any virus of interest and make it available as a third party “off the shelf” treatment for viral infections following transplantation. American Society of Gene & Cell Therapy 2017-03-08 /pmc/articles/PMC5415312/ /pubmed/28480300 http://dx.doi.org/10.1016/j.omtm.2017.02.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Dave, Hema
Luo, Min
Blaney, J.W.
Patel, Shabnum
Barese, Cecilia
Cruz, Conrad Russell
Shpall, Elizabeth J.
Bollard, Catherine M.
Hanley, Patrick J.
Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title_full Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title_fullStr Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title_full_unstemmed Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title_short Toward a Rapid Production of Multivirus-Specific T Cells Targeting BKV, Adenovirus, CMV, and EBV from Umbilical Cord Blood
title_sort toward a rapid production of multivirus-specific t cells targeting bkv, adenovirus, cmv, and ebv from umbilical cord blood
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415312/
https://www.ncbi.nlm.nih.gov/pubmed/28480300
http://dx.doi.org/10.1016/j.omtm.2017.02.001
work_keys_str_mv AT davehema towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT luomin towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT blaneyjw towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT patelshabnum towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT baresececilia towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT cruzconradrussell towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT shpallelizabethj towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT bollardcatherinem towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood
AT hanleypatrickj towardarapidproductionofmultivirusspecifictcellstargetingbkvadenoviruscmvandebvfromumbilicalcordblood