Evidence map›Paper›PMID 35600660›Full record

ArticleBioengineering & translational medicine2022

Predicting T-cell quality during manufacturing through an artificial intelligence-based integrative multiomics analytical platform.

Valerie Y Odeh-Couvertier, Nathan J Dwarshuis, Maxwell B Colonna, Bruce L Levine, Arthur S Edison, Theresa Kotanchek, Krishnendu Roy, Wandaliz Torres-Garcia

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. TiOBioprocess and biosystems engineering · 2026
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  11. Redefining quality in cell and gene therapies: Lessons from implementing electronic QMS in academic cGMP facility.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
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  13. Article
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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

8 authors.

Valerie Y Odeh-CouvertierDepartment of Industrial Engineering University of Puerto Rico Mayagüez Mayagüez Puerto Rico USA.
Nathan J DwarshuisThe Wallace H. Coulter Department of Biomedical Engineering Georgia Institute of Technology Atlanta Georgia USA.
Maxwell B ColonnaDepartments of Genetics and Biochemistry & Molecular Biology, Complex Carbohydrate Research Center University of Georgia Athens Georgia USA.
Bruce L LevineCenter for Cellular Immunotherapies, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA.
Arthur S EdisonDepartments of Genetics and Biochemistry & Molecular Biology, Complex Carbohydrate Research Center University of Georgia Athens Georgia USA.
Theresa KotanchekEvolved Analytics LLC Rancho Santa Fe California USA.
Krishnendu RoyThe Wallace H. Coulter Department of Biomedical Engineering Georgia Institute of Technology Atlanta Georgia USA.
Wandaliz Torres-GarciaDepartment of Industrial Engineering University of Puerto Rico Mayagüez Mayagüez Puerto Rico USA.ORCID https://orcid.org/0000-0001-7729-5554

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large-scale, reproducible manufacturing of therapeutic cells with consistently high quality is vital for translation to clinically effective and widely accessible cell therapies. However, the biological and logistical complexity of manufacturing a living product, including challenges associated with their inherent variability and uncertainties of process parameters, currently make it difficult to achieve predictable cell-product quality. Using a degradable microscaffold-based T-cell process, we developed an artificial intelligence (AI)-driven experimental-computational platform to identify a set of critical process parameters and critical quality attributes from heterogeneous, high-dimensional, time-dependent multiomics data, measurable during early stages of manufacturing and predictive of end-of-manufacturing product quality. Sequential, design-of-experiment-based studies, coupled with an agnostic machine-learning framework, were used to extract feature combinations from early in-culture media assessment that were highly predictive of the end-product CD4/CD8 ratio and total live CD4

Indexed as

artificial intelligencebioprocess optimizationcell therapy manufacturingcytokinesdesign of experimentsmetabolomicsT‐cell memory

Identifiers

PMID35600660
PMCPMC9115702

What OpenQuestion holds

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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.