Evidence map›Paper›PMID 35899783›Full record

ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2023

Microraft arrays for serial-killer CD19 chimeric antigen receptor T cells and single cell isolation.

Cody A LaBelle, Raymond J Zhang, Sally A Hunsucker, Paul M Armistead, Nancy L Allbritton

Open access · greenAbstract read
In one paragraph

Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

5 authors at 2 institutions in 1 country.

Cody A LaBelleJoint Department of Biomedical Engineering, University of North Carolina, Chapel Hill, North Carolina, USA.
Raymond J ZhangLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Sally A HunsuckerLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Paul M ArmisteadLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Nancy L AllbrittonDepartment of Bioengineering, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-9242-768X
University of North Carolina at Chapel Hill · USUniversity of Washington · US

Funding

MICROFABRICATED INSTRUMENTATION TO MEASURE SPHINGOLIPID SIGNALING IN HUMAN ACUTE MYELOID LEUKEMIAR01CA233811 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ALLBRITTON, NANCY L., ARMISTEAD, PAUL MICHAEL · 2019 to 2023
$3.1M
CellRaft Array for Screening and Isolation of Highly Effective Cytotoxic T CellsR42AI126905 · NIAID · CELL MICROSYSTEMS, INC. · PI ALLBRITTON, NANCY L., ARMISTEAD, PAUL MICHAEL · 2017 to 2018
$1.6M
NCI NIH HHS R01 CA233811NIAID NIH HHS R42 AI126905
6 · The paper itself

Abstract

Chimeric antigen receptor T (CAR-T) cell immunotherapies have seen success in treating hematological malignancies in recent years; however, the results can be highly variable. Single cell heterogeneity plays a key role in the variable efficacy of CAR-T cell treatments yet is largely unexplored. A major challenge is to understand the killing behavior and phenotype of individual CAR-T cells, which are able to serially kill targets. Thus, a platform capable of measuring time-dependent CAR-T cell mediated killing and then isolating single cells for downstream assays would be invaluable in characterizing CAR-T cells. An automated microraft array platform was designed to track CD19 CAR-T cell killing of CD19+ target cells and CAR-T cell motility over time followed by CAR-T cell collection based on killing behavior. The platform demonstrated automated CAR-T cell counting with up to 98% specificity and 96% sensitivity, and single cells were isolated with 89% efficiency. On average, 2.3% of single CAR-T cells were shown to participate in serial-killing of target cells, killing a maximum of three target cells in a 6 h period. The cytotoxicity and motility of >7000 individual CAR-T cells was tracked across four microraft arrays. The automated microraft array platform measured temporal cell-mediated cytotoxicity, CAR-T cell motility, CAR-T cell death, and CAR-T cell to target cell distances, followed by the capability to sort any desired CAR-T cell. The pipeline has the potential to further our understanding of T cell-based cancer immunotherapies and improve cell-therapy products for better patient outcomes.

Indexed as

Receptors, Chimeric AntigenCell SeparationImmunotherapyReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellReceptors, Chimeric AntigenCAR-T cellsimmunotherapymicrodevicesmicroraft arraysmicroscopysingle-cell

Identifiers

PMID35899783
PMCPMC9883594
OpenAlexW4288433412

What OpenQuestion holds

Textmetadata
LicenceTDM
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.