Evidence map›Paper›PMID 33898440›Full record

ArticleFrontiers in cell and developmental biology2021

Multi-Factor Clustering Incorporating Cell Motility Predicts T Cell Expansion Potential.

Joanne H Lee, Shuai Shao, Michelle Kim, Stacey M Fernandes, Jennifer R Brown, Lance C Kam

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. 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
0.3field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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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

6 authors at 2 institutions in 1 country.

Joanne H LeeDepartment of Biomedical Engineering, Columbia University, New York, NY, United States.
Shuai ShaoDepartment of Biomedical Engineering, Columbia University, New York, NY, United States.
Michelle KimDepartment of Biomedical Engineering, Columbia University, New York, NY, United States.
Stacey M FernandesDepartment of Medical Oncology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA, United States.
Jennifer R BrownDepartment of Medical Oncology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA, United States.
Lance C KamDepartment of Biomedical Engineering, Columbia University, New York, NY, United States.
Columbia University · USDana-Farber Cancer Institute · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
ProteomicsP01CA206978 · NCI · DANA-FARBER CANCER INST · PI CARR, STEVEN A · 2016 to 2025
$17.0M
Unlocking the Potential of PI3K Inhibition in CLLR01CA213442 · NCI · DANA-FARBER CANCER INST · PI BROWN, JENNIFER R · 2017 to 2021
$2.9M
Advanced Rigidity-based Material for Enhanced ImmunotherapyR01AI110593 · NIAID · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KAM, LANCE C · 2015 to 2018
$1.6M
Sample Sparing Chambers for Imaging of T cell Response and FunctionU24AI118669 · NIAID · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI KAM, LANCE C · 2015 to 2018
$1.2M
NCI NIH HHS P01 CA206978NCI NIH HHS P30 CA013696NCI NIH HHS R01 CA213442NIAID NIH HHS R01 AI110593NIAID NIH HHS U24 AI118669
6 · The paper itself

Abstract

Expansion of an initial population of T cells is essential for cellular immunotherapy. In Chronic Lymphocytic Leukemia (CLL), expansion is often complicated by lack of T cell proliferation, as these cells frequently show signs of exhaustion. This report seeks to identify specific biomarkers or measures of cell function that capture the proliferative potential of a starting population of cells. Mixed CD4+/CD8+ T cells from healthy donors and individuals previously treated for CLL were characterized on the basis of proliferative potential and

Indexed as

cell migrationimmunotherapyLeukemiamachine learningT cell

Identifiers

PMID33898440
PMCPMC8063612
OpenAlexW3156235263

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.