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A Modified Injector and Sample Acquisition Protocol Can Improve Data Quality and Reduce Inter-Instrument Variability of the Helios Mass Cytometer.
Lee, Brian H; Kelly, Geoffrey; Bradford, Shermineh; Davila, Melanie; Guo, Xinzheng V; Amir, El-Ad David; Thrash, Emily M; Solga, Michael D; Lannigan, Joanne; Sellers, Brian; Candia, Julian; Tsang, John; Montgomery, Ruth R; Tamaki, Stanley J; Sigdel, Tara K; Sarwal, Minnie M; Lanier, Lewis L; Tian, Yuan; Kim, Cheryl; Hinz, Denise; Peters, Bjoern; Sette, Alessandro; Rahman, Adeeb H.
Affiliation
  • Lee BH; Human Immune Monitoring Center, Icahn School of Medicine at Mt. Sinai, New York, New York.
  • Kelly G; Human Immune Monitoring Center, Icahn School of Medicine at Mt. Sinai, New York, New York.
  • Bradford S; Human Immune Monitoring Center, Icahn School of Medicine at Mt. Sinai, New York, New York.
  • Davila M; Human Immune Monitoring Center, Icahn School of Medicine at Mt. Sinai, New York, New York.
  • Guo XV; Human Immune Monitoring Center, Icahn School of Medicine at Mt. Sinai, New York, New York.
  • Amir ED; Astrolabe Diagnostics Inc., Fort Lee, New Jersey.
  • Thrash EM; Center for Immuno-Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Solga MD; Department of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, Virginia.
  • Lannigan J; Department of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, Virginia.
  • Sellers B; Trans-NIH Center for Human Immunology, Autoimmunity, and Inflammation, National Institutes of Health, Bethesda, Maryland.
  • Candia J; Trans-NIH Center for Human Immunology, Autoimmunity, and Inflammation, National Institutes of Health, Bethesda, Maryland.
  • Tsang J; Trans-NIH Center for Human Immunology, Autoimmunity, and Inflammation, National Institutes of Health, Bethesda, Maryland.
  • Montgomery RR; Department of Internal Medicine, School of Medicine, Yale University, New Haven, Connecticut.
  • Tamaki SJ; Department of Surgery, University of California San Francisco, San Francisco, California.
  • Sigdel TK; Department of Surgery, University of California San Francisco, San Francisco, California.
  • Sarwal MM; Department of Surgery, University of California San Francisco, San Francisco, California.
  • Lanier LL; Department of Microbiology and Immunology, University of California San Francisco, San Francisco, California.
  • Tian Y; Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, California.
  • Kim C; Flow Cytometry Core Facility, La Jolla Institute for Immunology, La Jolla.
  • Hinz D; Flow Cytometry Core Facility, La Jolla Institute for Immunology, La Jolla.
  • Peters B; Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, California.
  • Sette A; Department of Medicine, University of California San Diego, La Jolla, California.
  • Rahman AH; Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, California.
Cytometry A ; 95(9): 1019-1030, 2019 09.
Article in En | MEDLINE | ID: mdl-31364278
ABSTRACT
Mass cytometry is a powerful tool for high-dimensional single cell characterization. Since the introduction of the first commercial CyTOF mass cytometer by DVS Sciences in 2009, mass cytometry technology has matured and become more widely utilized, with sequential platform upgrades designed to address specific limitations and to expand the capabilities of the platform. Fluidigm's third-generation Helios mass cytometer introduced a number of upgrades over the previous CyTOF2. One of these new features is a modified narrow bore sample injector that generates smaller ion clouds, which is expected to improve sensitivity and throughput. However, following rigorous testing, we find that the narrow-bore sample injector may have unintended negative consequences on data quality and result in lower median and higher coefficients of variation in many antibody-associated signal intensities. We describe an alternative Helios acquisition protocol using a wider bore injector, which largely mitigates these data quality issues. We directly compare these two protocols in a multisite study of 10 Helios instruments across 7 institutions and show that the modified protocol improves data quality and reduces interinstrument variability. These findings highlight and address an important source of technical variability in mass cytometry experiments that is of particular relevance in the setting of multicenter studies. © 2019 International Society for Advancement of Cytometry.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Single-Cell Analysis / Flow Cytometry Type of study: Clinical_trials / Evaluation_studies Limits: Humans Language: En Journal: Cytometry A Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Single-Cell Analysis / Flow Cytometry Type of study: Clinical_trials / Evaluation_studies Limits: Humans Language: En Journal: Cytometry A Year: 2019 Document type: Article