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Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting

A general obstacle for clinical cell preparations is limited purity, which causes variability in the quality and potency of cell products and might be responsible for negative side effects due to unwanted contaminants. Highly pure populations can be obtained best using positive selection techniques....

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Detalles Bibliográficos
Autores principales: Stemberger, Christian, Dreher, Stefan, Tschulik, Claudia, Piossek, Christine, Bet, Jeannette, Yamamoto, Tori N., Schiemann, Matthias, Neuenhahn, Michael, Martin, Klaus, Schlapschy, Martin, Skerra, Arne, Schmidt, Thomas, Edinger, Matthias, Riddell, Stanley R., Germeroth, Lothar, Busch, Dirk H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335788/
https://www.ncbi.nlm.nih.gov/pubmed/22545138
http://dx.doi.org/10.1371/journal.pone.0035798
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author Stemberger, Christian
Dreher, Stefan
Tschulik, Claudia
Piossek, Christine
Bet, Jeannette
Yamamoto, Tori N.
Schiemann, Matthias
Neuenhahn, Michael
Martin, Klaus
Schlapschy, Martin
Skerra, Arne
Schmidt, Thomas
Edinger, Matthias
Riddell, Stanley R.
Germeroth, Lothar
Busch, Dirk H.
author_facet Stemberger, Christian
Dreher, Stefan
Tschulik, Claudia
Piossek, Christine
Bet, Jeannette
Yamamoto, Tori N.
Schiemann, Matthias
Neuenhahn, Michael
Martin, Klaus
Schlapschy, Martin
Skerra, Arne
Schmidt, Thomas
Edinger, Matthias
Riddell, Stanley R.
Germeroth, Lothar
Busch, Dirk H.
author_sort Stemberger, Christian
collection PubMed
description A general obstacle for clinical cell preparations is limited purity, which causes variability in the quality and potency of cell products and might be responsible for negative side effects due to unwanted contaminants. Highly pure populations can be obtained best using positive selection techniques. However, in many cases target cell populations need to be segregated from other cells by combinations of multiple markers, which is still difficult to achieve – especially for clinical cell products. Therefore, we have generated low-affinity antibody-derived Fab-fragments, which stain like parental antibodies when multimerized via Strep-tag and Strep-Tactin, but can subsequently be removed entirely from the target cell population. Such reagents can be generated for virtually any antigen and can be used for sequential positive enrichment steps via paramagnetic beads. First protocols for multiparameter enrichment of two clinically relevant cell populations, CD4(high)/CD25(high)/CD45RA(high) ‘regulatory T cells’ and CD8(high)/CD62L(high)/CD45RA(neg) ‘central memory T cells’, have been established to determine quality and efficacy parameters of this novel technology, which should have broad applicability for clinical cell sorting as well as basic research.
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spelling pubmed-33357882012-04-27 Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting Stemberger, Christian Dreher, Stefan Tschulik, Claudia Piossek, Christine Bet, Jeannette Yamamoto, Tori N. Schiemann, Matthias Neuenhahn, Michael Martin, Klaus Schlapschy, Martin Skerra, Arne Schmidt, Thomas Edinger, Matthias Riddell, Stanley R. Germeroth, Lothar Busch, Dirk H. PLoS One Research Article A general obstacle for clinical cell preparations is limited purity, which causes variability in the quality and potency of cell products and might be responsible for negative side effects due to unwanted contaminants. Highly pure populations can be obtained best using positive selection techniques. However, in many cases target cell populations need to be segregated from other cells by combinations of multiple markers, which is still difficult to achieve – especially for clinical cell products. Therefore, we have generated low-affinity antibody-derived Fab-fragments, which stain like parental antibodies when multimerized via Strep-tag and Strep-Tactin, but can subsequently be removed entirely from the target cell population. Such reagents can be generated for virtually any antigen and can be used for sequential positive enrichment steps via paramagnetic beads. First protocols for multiparameter enrichment of two clinically relevant cell populations, CD4(high)/CD25(high)/CD45RA(high) ‘regulatory T cells’ and CD8(high)/CD62L(high)/CD45RA(neg) ‘central memory T cells’, have been established to determine quality and efficacy parameters of this novel technology, which should have broad applicability for clinical cell sorting as well as basic research. Public Library of Science 2012-04-24 /pmc/articles/PMC3335788/ /pubmed/22545138 http://dx.doi.org/10.1371/journal.pone.0035798 Text en Stemberger et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Stemberger, Christian
Dreher, Stefan
Tschulik, Claudia
Piossek, Christine
Bet, Jeannette
Yamamoto, Tori N.
Schiemann, Matthias
Neuenhahn, Michael
Martin, Klaus
Schlapschy, Martin
Skerra, Arne
Schmidt, Thomas
Edinger, Matthias
Riddell, Stanley R.
Germeroth, Lothar
Busch, Dirk H.
Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title_full Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title_fullStr Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title_full_unstemmed Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title_short Novel Serial Positive Enrichment Technology Enables Clinical Multiparameter Cell Sorting
title_sort novel serial positive enrichment technology enables clinical multiparameter cell sorting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335788/
https://www.ncbi.nlm.nih.gov/pubmed/22545138
http://dx.doi.org/10.1371/journal.pone.0035798
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