Evidence map›Paper›PMID 37172572›Full record

ReviewTrends in pharmacological sciences2023

Biophysical and mechanobiological considerations for T-cell-based immunotherapy.

Chuzhi Zhuang, Jared E Gould, Archibald Enninful, Stephanie Shao, Michael Mak

Abstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  8. Mechanoregulation of lymphocyte cytotoxicity.Nature reviews. Immunology · 2025
    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

5 authors.

Chuzhi ZhuangDepartment of Biomedical Engineering, Yale University, New Haven, CT 06511, USA.
Jared E GouldDepartment of Biomedical Engineering, Yale University, New Haven, CT 06511, USA.
Archibald EnninfulDepartment of Biomedical Engineering, Yale University, New Haven, CT 06511, USA.
Stephanie ShaoDepartment of Biomedical Engineering, Yale University, New Haven, CT 06511, USA.
Michael MakDepartment of Biomedical Engineering, Yale University, New Haven, CT 06511, USA. Electronic address: michael.mak@yale.edu.

Funding

(PQ5) Mitochondrial Heterogeneity in Melanoma Tumor and Immune ResponsesR01CA216101 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GERALD SHADEL · 2018 to 2026
$5.0M
TRANSFER GRANT: Systems Biophysics of Multiscale State Transitions in Cells and TissuesR35GM142875 · NIGMS · YALE UNIVERSITY · PI Michael MAK · 2021 to 2026
$2.7M
NCI NIH HHS R01 CA216101NIGMS NIH HHS R35 GM142875
6 · The paper itself

Abstract

Immunotherapies modulate the body's defense system to treat cancer. While these therapies have shown efficacy against multiple types of cancer, patient response rates are limited, and the off-target effects can be severe. Typical approaches in developing immunotherapies tend to focus on antigen targeting and molecular signaling, while overlooking biophysical and mechanobiological effects. Immune cells and tumor cells are both responsive to biophysical cues, which are prominent in the tumor microenvironment. Recent studies have shown that mechanosensing - including through Piezo1, adhesions, and Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) - influences tumor-immune interactions and immunotherapeutic efficacy. Furthermore, biophysical methods such as fluidic systems and mechanoactivation schemes can improve the controllability and manufacturing of engineered T cells, with potential for increasing therapeutic efficacy and specificity. This review focuses on leveraging advances in immune biophysics and mechanobiology toward improving chimeric antigen receptor (CAR) T-cell and anti-programmed cell death protein 1 (anti-PD-1) therapies.

Indexed as

NeoplasmsT-LymphocytesBiophysicsHumansImmunotherapyImmunotherapy, AdoptiveIon ChannelsTranscription FactorsTumor MicroenvironmentIon ChannelsPIEZO1 protein, humanTranscription FactorsbiophysicsCAR-TimmunotherapymechanobiologyPD-1

Identifiers

PMID37172572
PMCPMC10188210

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.