Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards
Many anticancer therapies such as antibody-based therapies, cellular therapeutics (e.g., genetically modified cells, regulators of cytokine signaling, and signal transduction), and other biologically tailored interventions strongly influence the immune system and require tools for research, diagnosi...
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doaj-73f9781db4b644258504c9ea23e167852020-11-25T03:06:46ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-09-011110.3389/fimmu.2020.02169529893Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and StandardsClaude Lambert0Gulderen Yanikkaya Demirel1Thomas Keller2Frank Preijers3Katherina Psarra4Matthias Schiemann5Mustafa Özçürümez6Ulrich Sack7University Hospital, Immunology Laboratory, FRE-CNRS 3312, Saint-Etienne, FranceStem Cell Laboratory, Immunology Department, Faculty of Medicine, Yeditepe University, Istanbul, TurkeyAcomed Statistik, Leipzig, GermanyLaboratory of Hematology, Department of Laboratory Medicine, Radboud University Medical Center, Nijmegen, NetherlandsDepartment of Immunology-Histocompatibility, Evangelismos Hospital, Athens, GreeceInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, GermanyUniversitätsklinikum Knappschaftskrankenhaus Bochum, Bochum, GermanyMedizinische Fakultät, Institut für Klinische Immunologie, Universität Leipzig, Leipzig, GermanyMany anticancer therapies such as antibody-based therapies, cellular therapeutics (e.g., genetically modified cells, regulators of cytokine signaling, and signal transduction), and other biologically tailored interventions strongly influence the immune system and require tools for research, diagnosis, and monitoring. In flow cytometry, in vitro diagnostic (IVD) test kits that have been compiled and validated by the manufacturer are not available for all requirements. Laboratories are therefore usually dependent on modifying commercially available assays or, most often, developing them to meet clinical needs. However, both variants must then undergo full validation to fulfill the IVD regulatory requirements. Flow cytometric immunophenotyping is a multiparametric analysis of parameters, some of which have to be repeatedly adjusted; that must be considered when developing specific antibody panels. Careful adjustments of general rules are required to meet legal and regulatory requirements in the analysis of these assays. Here, we describe the relevant regulatory framework for flow cytometry-based assays and describe methods for the introduction of new antibody combinations into routine work including development of performance specifications, validation, and statistical methodology for design and analysis of the experiments. The aim is to increase reliability, efficiency, and auditability after the introduction of in-house-developed flow cytometry assays.https://www.frontiersin.org/article/10.3389/fimmu.2020.02169/fullflow cytometryproceduresaccreditationquality controllaboratory diagnosticsvalidation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Claude Lambert Gulderen Yanikkaya Demirel Thomas Keller Frank Preijers Katherina Psarra Matthias Schiemann Mustafa Özçürümez Ulrich Sack |
spellingShingle |
Claude Lambert Gulderen Yanikkaya Demirel Thomas Keller Frank Preijers Katherina Psarra Matthias Schiemann Mustafa Özçürümez Ulrich Sack Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards Frontiers in Immunology flow cytometry procedures accreditation quality control laboratory diagnostics validation |
author_facet |
Claude Lambert Gulderen Yanikkaya Demirel Thomas Keller Frank Preijers Katherina Psarra Matthias Schiemann Mustafa Özçürümez Ulrich Sack |
author_sort |
Claude Lambert |
title |
Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards |
title_short |
Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards |
title_full |
Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards |
title_fullStr |
Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards |
title_full_unstemmed |
Flow Cytometric Analyses of Lymphocyte Markers in Immune Oncology: A Comprehensive Guidance for Validation Practice According to Laws and Standards |
title_sort |
flow cytometric analyses of lymphocyte markers in immune oncology: a comprehensive guidance for validation practice according to laws and standards |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2020-09-01 |
description |
Many anticancer therapies such as antibody-based therapies, cellular therapeutics (e.g., genetically modified cells, regulators of cytokine signaling, and signal transduction), and other biologically tailored interventions strongly influence the immune system and require tools for research, diagnosis, and monitoring. In flow cytometry, in vitro diagnostic (IVD) test kits that have been compiled and validated by the manufacturer are not available for all requirements. Laboratories are therefore usually dependent on modifying commercially available assays or, most often, developing them to meet clinical needs. However, both variants must then undergo full validation to fulfill the IVD regulatory requirements. Flow cytometric immunophenotyping is a multiparametric analysis of parameters, some of which have to be repeatedly adjusted; that must be considered when developing specific antibody panels. Careful adjustments of general rules are required to meet legal and regulatory requirements in the analysis of these assays. Here, we describe the relevant regulatory framework for flow cytometry-based assays and describe methods for the introduction of new antibody combinations into routine work including development of performance specifications, validation, and statistical methodology for design and analysis of the experiments. The aim is to increase reliability, efficiency, and auditability after the introduction of in-house-developed flow cytometry assays. |
topic |
flow cytometry procedures accreditation quality control laboratory diagnostics validation |
url |
https://www.frontiersin.org/article/10.3389/fimmu.2020.02169/full |
work_keys_str_mv |
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