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The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study

The validation of assays that quantify antigen-specific T cell responses is critically dependent on cell samples that contain clearly defined measurable numbers of antigen-specific T cells. An important requirement is that such cell samples are handled and analyzed in a comparable fashion to periphe...

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Autores principales: Singh, Satwinder Kaur, Tummers, Bart, Schumacher, Ton N., Gomez, Raquel, Franken, Kees L. M. C., Verdegaal, Els M., Laske, Karoline, Gouttefangeas, Cécile, Ottensmeier, Christian, Welters, Marij J. P., Britten, Cedrik M., van der Burg, Sjoerd H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589624/
https://www.ncbi.nlm.nih.gov/pubmed/22986454
http://dx.doi.org/10.1007/s00262-012-1351-0
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author Singh, Satwinder Kaur
Tummers, Bart
Schumacher, Ton N.
Gomez, Raquel
Franken, Kees L. M. C.
Verdegaal, Els M.
Laske, Karoline
Gouttefangeas, Cécile
Ottensmeier, Christian
Welters, Marij J. P.
Britten, Cedrik M.
van der Burg, Sjoerd H.
author_facet Singh, Satwinder Kaur
Tummers, Bart
Schumacher, Ton N.
Gomez, Raquel
Franken, Kees L. M. C.
Verdegaal, Els M.
Laske, Karoline
Gouttefangeas, Cécile
Ottensmeier, Christian
Welters, Marij J. P.
Britten, Cedrik M.
van der Burg, Sjoerd H.
author_sort Singh, Satwinder Kaur
collection PubMed
description The validation of assays that quantify antigen-specific T cell responses is critically dependent on cell samples that contain clearly defined measurable numbers of antigen-specific T cells. An important requirement is that such cell samples are handled and analyzed in a comparable fashion to peripheral blood mononuclear cells (PBMC). We performed a proof-of-principle study to show that retrovirally TCR-transduced T cells spiked at defined numbers in autologous PBMC can be used as standard samples for HLA/peptide multimer staining. NY-ESO-1(157–165)-specific, TCR-transduced CD8+ T cell batches were successfully generated from PBMC of several HLA-A*0201 healthy donors, purified by magnetic cell sorting on the basis of HLA tetramer (TM) staining and expanded with specific antigen in vitro. When subsequently spiked into autologous PBMC, the detection of these CD3+CD8+TM+ T cells was highly accurate with a mean accuracy of 91.6 %. The standard cells can be preserved for a substantial period of time in liquid nitrogen. Furthermore, TM staining of fresh and cryopreserved standard samples diluted at decreasing concentrations into autologous cryopreserved unspiked PBMC revealed that the spiked CD3+CD8+TM+ T cells could be accurately detected at all dilutions in a linear fashion with a goodness-of-fit of over 0.99 at a frequency of at least 0.02 % among the CD3+CD8+ T cell population. Notably, the CD3+CD8+TM+ cells of the standard samples were located exactly within the gates used to analyze patient samples and displayed a similar scatter pattern. The performance of the cryopreserved standard samples in the hands of 5 external investigators was good with an inter-laboratory variation of 32.9 % and the doubtless identification of one outlier. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00262-012-1351-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-35896242013-03-07 The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study Singh, Satwinder Kaur Tummers, Bart Schumacher, Ton N. Gomez, Raquel Franken, Kees L. M. C. Verdegaal, Els M. Laske, Karoline Gouttefangeas, Cécile Ottensmeier, Christian Welters, Marij J. P. Britten, Cedrik M. van der Burg, Sjoerd H. Cancer Immunol Immunother Original Article The validation of assays that quantify antigen-specific T cell responses is critically dependent on cell samples that contain clearly defined measurable numbers of antigen-specific T cells. An important requirement is that such cell samples are handled and analyzed in a comparable fashion to peripheral blood mononuclear cells (PBMC). We performed a proof-of-principle study to show that retrovirally TCR-transduced T cells spiked at defined numbers in autologous PBMC can be used as standard samples for HLA/peptide multimer staining. NY-ESO-1(157–165)-specific, TCR-transduced CD8+ T cell batches were successfully generated from PBMC of several HLA-A*0201 healthy donors, purified by magnetic cell sorting on the basis of HLA tetramer (TM) staining and expanded with specific antigen in vitro. When subsequently spiked into autologous PBMC, the detection of these CD3+CD8+TM+ T cells was highly accurate with a mean accuracy of 91.6 %. The standard cells can be preserved for a substantial period of time in liquid nitrogen. Furthermore, TM staining of fresh and cryopreserved standard samples diluted at decreasing concentrations into autologous cryopreserved unspiked PBMC revealed that the spiked CD3+CD8+TM+ T cells could be accurately detected at all dilutions in a linear fashion with a goodness-of-fit of over 0.99 at a frequency of at least 0.02 % among the CD3+CD8+ T cell population. Notably, the CD3+CD8+TM+ cells of the standard samples were located exactly within the gates used to analyze patient samples and displayed a similar scatter pattern. The performance of the cryopreserved standard samples in the hands of 5 external investigators was good with an inter-laboratory variation of 32.9 % and the doubtless identification of one outlier. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00262-012-1351-0) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-09-18 2013 /pmc/articles/PMC3589624/ /pubmed/22986454 http://dx.doi.org/10.1007/s00262-012-1351-0 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Singh, Satwinder Kaur
Tummers, Bart
Schumacher, Ton N.
Gomez, Raquel
Franken, Kees L. M. C.
Verdegaal, Els M.
Laske, Karoline
Gouttefangeas, Cécile
Ottensmeier, Christian
Welters, Marij J. P.
Britten, Cedrik M.
van der Burg, Sjoerd H.
The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title_full The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title_fullStr The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title_full_unstemmed The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title_short The development of standard samples with a defined number of antigen-specific T cells to harmonize T cell assays: a proof-of-principle study
title_sort development of standard samples with a defined number of antigen-specific t cells to harmonize t cell assays: a proof-of-principle study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589624/
https://www.ncbi.nlm.nih.gov/pubmed/22986454
http://dx.doi.org/10.1007/s00262-012-1351-0
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