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A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes

High-dimensional flow cytometry is the gold standard to study the human immune system in large cohorts. However, large sample sizes increase inter-experimental variation because of technical and experimental inaccuracies introduced by batch variability. Our high-throughput sample processing pipeline...

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Autores principales: Liechti, Thomas, Van Gassen, Sofie, Beddall, Margaret, Ballard, Reid, Iftikhar, Yaser, Du, Renguang, Venkataraman, Thiagarajan, Novak, David, Mangino, Massimo, Perfetto, Stephen, Larman, H. Benjamin, Spector, Tim, Saeys, Yvan, Roederer, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626267/
https://www.ncbi.nlm.nih.gov/pubmed/37883924
http://dx.doi.org/10.1016/j.crmeth.2023.100619
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author Liechti, Thomas
Van Gassen, Sofie
Beddall, Margaret
Ballard, Reid
Iftikhar, Yaser
Du, Renguang
Venkataraman, Thiagarajan
Novak, David
Mangino, Massimo
Perfetto, Stephen
Larman, H. Benjamin
Spector, Tim
Saeys, Yvan
Roederer, Mario
author_facet Liechti, Thomas
Van Gassen, Sofie
Beddall, Margaret
Ballard, Reid
Iftikhar, Yaser
Du, Renguang
Venkataraman, Thiagarajan
Novak, David
Mangino, Massimo
Perfetto, Stephen
Larman, H. Benjamin
Spector, Tim
Saeys, Yvan
Roederer, Mario
author_sort Liechti, Thomas
collection PubMed
description High-dimensional flow cytometry is the gold standard to study the human immune system in large cohorts. However, large sample sizes increase inter-experimental variation because of technical and experimental inaccuracies introduced by batch variability. Our high-throughput sample processing pipeline in combination with 28-color flow cytometry focuses on increased throughput (192 samples/experiment) and high reproducibility. We implemented quality control checkpoints to reduce technical and experimental variation. Finally, we integrated FlowSOM clustering to facilitate automated data analysis and demonstrate the reproducibility of our pipeline in a study with 3,357 samples. We reveal age-associated immune dynamics in 2,300 individuals, signified by decreasing T and B cell subsets with age. In addition, by combining genetic analyses, our approach revealed unique immune signatures associated with a single nucleotide polymorphism (SNP) that abrogates CD45 isoform splicing. In summary, we provide a versatile and reliable high-throughput, flow cytometry-based pipeline for immune discovery and exploration in large cohorts.
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spelling pubmed-106262672023-11-07 A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes Liechti, Thomas Van Gassen, Sofie Beddall, Margaret Ballard, Reid Iftikhar, Yaser Du, Renguang Venkataraman, Thiagarajan Novak, David Mangino, Massimo Perfetto, Stephen Larman, H. Benjamin Spector, Tim Saeys, Yvan Roederer, Mario Cell Rep Methods Article High-dimensional flow cytometry is the gold standard to study the human immune system in large cohorts. However, large sample sizes increase inter-experimental variation because of technical and experimental inaccuracies introduced by batch variability. Our high-throughput sample processing pipeline in combination with 28-color flow cytometry focuses on increased throughput (192 samples/experiment) and high reproducibility. We implemented quality control checkpoints to reduce technical and experimental variation. Finally, we integrated FlowSOM clustering to facilitate automated data analysis and demonstrate the reproducibility of our pipeline in a study with 3,357 samples. We reveal age-associated immune dynamics in 2,300 individuals, signified by decreasing T and B cell subsets with age. In addition, by combining genetic analyses, our approach revealed unique immune signatures associated with a single nucleotide polymorphism (SNP) that abrogates CD45 isoform splicing. In summary, we provide a versatile and reliable high-throughput, flow cytometry-based pipeline for immune discovery and exploration in large cohorts. Elsevier 2023-10-25 /pmc/articles/PMC10626267/ /pubmed/37883924 http://dx.doi.org/10.1016/j.crmeth.2023.100619 Text en https://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 Article
Liechti, Thomas
Van Gassen, Sofie
Beddall, Margaret
Ballard, Reid
Iftikhar, Yaser
Du, Renguang
Venkataraman, Thiagarajan
Novak, David
Mangino, Massimo
Perfetto, Stephen
Larman, H. Benjamin
Spector, Tim
Saeys, Yvan
Roederer, Mario
A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title_full A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title_fullStr A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title_full_unstemmed A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title_short A robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
title_sort robust pipeline for high-content, high-throughput immunophenotyping reveals age- and genetics-dependent changes in blood leukocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626267/
https://www.ncbi.nlm.nih.gov/pubmed/37883924
http://dx.doi.org/10.1016/j.crmeth.2023.100619
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