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OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel
This Optimized Multicolor Immunofluorescence Panel was designed to identify and quantify all principal leukocyte populations in human blood using a minimum number of markers. We achieved this goal using a carefully selected combination of 14 surface markers compatible with standard flow cytometric i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292053/ https://www.ncbi.nlm.nih.gov/pubmed/34260151 http://dx.doi.org/10.1002/cyto.a.24481 |
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author | Boesch, Maximilian Sykora, Martina Gasteiger, Silvia Baty, Florent Brutsche, Martin H. Sopper, Sieghart |
author_facet | Boesch, Maximilian Sykora, Martina Gasteiger, Silvia Baty, Florent Brutsche, Martin H. Sopper, Sieghart |
author_sort | Boesch, Maximilian |
collection | PubMed |
description | This Optimized Multicolor Immunofluorescence Panel was designed to identify and quantify all principal leukocyte populations in human blood using a minimum number of markers. We achieved this goal using a carefully selected combination of 14 surface markers compatible with standard flow cytometric instruments and accessible to a particularly large research community. Optimized for use in whole blood, this panel allows polymorphonuclear cell identification, supports live cell recovery, and is well‐suited for absolute cell counting applications in the original in vivo volume. Panel performance and the separation of populations are high, and virtually no cells remain undefined after gating. Besides the identification of neutrophils, eosinophils, basophils, T cells, natural killer cells, B cells, plasma cells, monocytes, myeloid dendritic cells and plasmacytoid dendritic cells, this panel also covers progenitor cells and may therefore be attractive for stem cell researchers. Envisioned applications of this panel include immune monitoring within clinical trials, initial discovery to inform subset‐targeted panels, and clinical diagnostics. In summary, this panel offers a broadly applicable platform for immune cell identification, quantification and characterization in human samples, particularly whole blood. |
format | Online Article Text |
id | pubmed-9292053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92920532022-07-20 OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel Boesch, Maximilian Sykora, Martina Gasteiger, Silvia Baty, Florent Brutsche, Martin H. Sopper, Sieghart Cytometry A Omip This Optimized Multicolor Immunofluorescence Panel was designed to identify and quantify all principal leukocyte populations in human blood using a minimum number of markers. We achieved this goal using a carefully selected combination of 14 surface markers compatible with standard flow cytometric instruments and accessible to a particularly large research community. Optimized for use in whole blood, this panel allows polymorphonuclear cell identification, supports live cell recovery, and is well‐suited for absolute cell counting applications in the original in vivo volume. Panel performance and the separation of populations are high, and virtually no cells remain undefined after gating. Besides the identification of neutrophils, eosinophils, basophils, T cells, natural killer cells, B cells, plasma cells, monocytes, myeloid dendritic cells and plasmacytoid dendritic cells, this panel also covers progenitor cells and may therefore be attractive for stem cell researchers. Envisioned applications of this panel include immune monitoring within clinical trials, initial discovery to inform subset‐targeted panels, and clinical diagnostics. In summary, this panel offers a broadly applicable platform for immune cell identification, quantification and characterization in human samples, particularly whole blood. John Wiley & Sons, Inc. 2021-07-14 2022-01 /pmc/articles/PMC9292053/ /pubmed/34260151 http://dx.doi.org/10.1002/cyto.a.24481 Text en © 2021 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Omip Boesch, Maximilian Sykora, Martina Gasteiger, Silvia Baty, Florent Brutsche, Martin H. Sopper, Sieghart OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title | OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title_full | OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title_fullStr | OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title_full_unstemmed | OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title_short | OMIP 077: Definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
title_sort | omip 077: definition of all principal human leukocyte populations using a broadly applicable 14‐color panel |
topic | Omip |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292053/ https://www.ncbi.nlm.nih.gov/pubmed/34260151 http://dx.doi.org/10.1002/cyto.a.24481 |
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