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What's Normal? Using Standardized Flow Cytometry Immunophenotyping to Create Comprehensive Pediatric Reference Ranges

2018· article· en· W2884434186 on OpenAlexaff
Anne Halpin, Morgan Sosniuk, Juanita Wizniak, Artur Szkotak, Simon Urschel, Lori J. West

Bibliographic record

VenueTransplantation · 2018
Typearticle
Languageen
FieldImmunology and Microbiology
TopicImmune Cell Function and Interaction
Canadian institutionsUniversity of Alberta HospitalAlberta Hospital EdmontonUniversity of AlbertaAlberta Health Services
Fundersnot available
KeywordsImmunophenotypingFlow cytometryMedicineCytometryHematologyReference valuesImmunologyPathologyInternal medicine

Abstract

fetched live from OpenAlex

Studying pediatric patients includes challenges such as difficulty obtaining samples, limited normal control reference data and small available sample volumes. Standardized flow cytometry immunophenotyping panels are commercially available to explore lymphocyte markers and extensive normal adult ranges have been published by the ONE Study group; comparable pediatric control data do not exist. Our objective is to establish a reference dataset to be available for pediatric studies using standardized, comprehensive flow cytometry panels with fresh whole blood. Our group had the opportunity to collaborate with the local clinical hematology laboratory to obtain normal pediatric samples with the goal of establishing comprehensive reference ranges across the pediatric age spectrum. This study also acted as a trial of this methodology for potential implementation in the clinical laboratory. Methods Using 700uL of EDTA blood, DuraClone IM (Beckman Coulter) flow cytometry phenotyping was performed on healthy pediatric controls ranging from 66 days to 16 years of age (n=10). Samples were tested in five, 10-colour flow cytometry T and B cell panels. Acquisition was performed on a Navios cytometer following calibration and standardization of cytometer output by Flow-Set™ Pro Fluorospheres. Analysis of the markers programmed cell death protein 1 (PD-1), often noted as a measure of T cell exhaustion, and gamma/delta (γδ) T cells and their associated markers Vd1 and Vd2, was performed. Results Preliminary analyses show age related trends in PD-1 + T cells with increasing PD-1+ CD4 T cells with increasing age as shown in Figure 1 (R2=0.701); this association is much weaker for CD8 T cells. The number of CD3+ T cells, including γδ T cells, decreases with age, while the % of each population of cells remains constant. There is a trend indicating a decreasing ratio of V delta 1 to V delta 2 γδ T cells with age. Conclusion Duraclone is a rapid immunophenotyping method that requires small blood volumes. These results begin to establish valuable reference data for pediatric transplant patient populations and suggest that these flow panels show promise for application in the clinical flow cytometry laboratory due to their standardized nature. We will continue to explore age-related trends as we analyse additional data from these controls and test additional samples. Complete blood count data are available to calculate absolute cell counts and this analysis will be performed. The use of fresh whole blood in this project differs from published pediatric reference range studies utilizing frozen cells and ensures populations are not lost or altered during mononuclear cell isolation or freeze thaw cycles. This study highlights the value of partnership between research and clinical laboratories as it can facilitate access to otherwise difficult to obtain samples and is valuable to the clinical laboratory in the exploration of new methodologies. Women and Children's Health Reseach Institute (WCHRI).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.008
metaresearch head score (Gemma)0.015
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.044

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0080.015
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0030.002
Science and technology studies0.0010.001
Scholarly communication0.0020.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.032
GPT teacher head0.288
Teacher spread0.256 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2018
Admission routes1
Has abstractyes

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