Evidence map›Paper›PMID 28550117›Full record

ArticleJournal of leukocyte biology2017

Comparative exploration of multidimensional flow cytometry software: a model approach evaluating T cell polyfunctional behavior.

Timothy T Spear, Michael I Nishimura, Patricia E Simms

Abstract readComparative Study
In one paragraph

Article in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Computational Analysis of Multiparametric Flow Cytometric Data to Dissect B Cell Subsets in Vaccine Studies.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2020
    Article
  3. Article
  4. Altered Peptide Ligands Impact the Diversity of Polyfunctional Phenotypes in T Cell Receptor Gene-Modified T Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Timothy T SpearDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, Maywood, Illinois, USA; and.
Michael I NishimuraDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, Maywood, Illinois, USA; and.
Patricia E SimmsFlow Cytometry Core Facility, Office of Research Services, Loyola University Chicago, Maywood, Illinois, USA psimms@luc.edu.

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
TCR Affinity and Therapeutic Efficacy of T CellsR01CA104947 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NISHIMURA, MICHAEL I. · 2007 to 2011
$1.9M
Animal Model for Her-2/neu Specific TCR Gene TransferR01CA102280 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2003 to 2007
$1.4M
Tumor Recognition by TCR Transduced CD4+ and CD8+T CellsR01CA090873 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2001 to 2004
$1.3M
TCR Gene Transfer for Treating HCV-Associated MalignanciesF30CA180731 · NCI · LOYOLA UNIVERSITY CHICAGO · PI SPEAR, TIMOTHY · 2014 to 2018
$154k
NCI NIH HHS F30 CA180731NCI NIH HHS P01 CA154778NCI NIH HHS R01 CA090873NCI NIH HHS R01 CA102280NCI NIH HHS R01 CA104947
6 · The paper itself

Abstract

Advancement in flow cytometry reagents and instrumentation has allowed for simultaneous analysis of large numbers of lineage/functional immune cell markers. Highly complex datasets generated by polychromatic flow cytometry require proper analytical software to answer investigators' questions. A problem among many investigators and flow cytometry Shared Resource Laboratories (SRLs), including our own, is a lack of access to a flow cytometry-knowledgeable bioinformatics team, making it difficult to learn and choose appropriate analysis tool(s). Here, we comparatively assess various multidimensional flow cytometry software packages for their ability to answer a specific biologic question and provide graphical representation output suitable for publication, as well as their ease of use and cost. We assessed polyfunctional potential of TCR-transduced T cells, serving as a model evaluation, using multidimensional flow cytometry to analyze 6 intracellular cytokines and degranulation on a per-cell basis. Analysis of 7 parameters resulted in 128 possible combinations of positivity/negativity, far too complex for basic flow cytometry software to analyze fully. Various software packages were used, analysis methods used in each described, and representative output displayed. Of the tools investigated, automated classification of cellular expression by nonlinear stochastic embedding (ACCENSE) and coupled analysis in Pestle/simplified presentation of incredibly complex evaluations (SPICE) provided the most user-friendly manipulations and readable output, evaluating effects of altered antigen-specific stimulation on T cell polyfunctionality. This detailed approach may serve as a model for other investigators/SRLs in selecting the most appropriate software to analyze complex flow cytometry datasets. Further development and awareness of available tools will help guide proper data analysis to answer difficult biologic questions arising from incredibly complex datasets.

Indexed as

SoftwareComputational BiologyFlow CytometryFluorescent Antibody TechniqueHumansT-LymphocytesACCENSEcomputational biology/bioinformaticsPestlepolychromatic flow cytometrySPICE

Identifiers

PMID28550117
PMCPMC6608077

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.