Evidence map›Paper›PMID 36645182›Full record

ArticleAdvanced healthcare materials2023

Cell-Sized Lipid Vesicles as Artificial Antigen-Presenting Cells for Antigen-Specific T Cell Activation.

Jui-Yi Chen, Sudhanshu Agrawal, Hsiu-Ping Yi, Derek Vallejo, Anshu Agrawal, Abraham P Lee

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  6. Solvent-Mediated Dewetting Principles for Cell-Sized Liposome Formation.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  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

6 authors at 1 institution in 1 country.

Jui-Yi ChenBiomedical Engineering, University of California, Irvine, CA, 92617, USA.
Sudhanshu AgrawalDepartment of Medicine, University of California, Irvine, CA, 92617, USA.
Hsiu-Ping YiBiomedical Engineering, University of California, Irvine, CA, 92617, USA.
Derek VallejoBiomedical Engineering, University of California, Irvine, CA, 92617, USA.
Anshu AgrawalDepartment of Medicine, University of California, Irvine, CA, 92617, USA.
Abraham P LeeBiomedical Engineering, University of California, Irvine, CA, 92617, USA.ORCID 0000-0001-8378-6616
University of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Microfluidic Precision Engineered Artificial Antigen Presenting Cells for Cancer ImmunotherapyR33CA267258 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI AGRAWAL, ANSHU, LEE, ABRAHAM P · 2022 to 2025
$1.1M
Microfluidic Engineering of Artificial-Antigen Presenting Cells for the Biomanufacturing of Tumor-Specific T-CellsR21EB026900 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI LEE, ABRAHAM P · 2018 to 2019
$392k
NCI NIH HHS P30 CA062203NCI NIH HHS R33 CA267258NIBIB NIH HHS 1R21EB026900NIBIB NIH HHS R21 EB026900
6 · The paper itself

Abstract

In this study, efficient T cell activation is demonstrated using cell-sized artificial antigen-presenting cells (aAPCs) with protein-conjugated bilayer lipid membranes that mimic biological cell membranes. The highly uniform aAPCs are generated by a facile method based on standard droplet microfluidic devices. These aAPCs are able to activate the T cells in peripheral blood mononuclear cells, showing a 28-fold increase in interferon gamma (IFNγ) secretion, a 233-fold increase in antigen-specific CD8 T cells expansion, and a 16-fold increase of CD4 T cell expansion. The aAPCs do not require repetitive boosting or additional stimulants and can function at a relatively low aAPC-to-T cell ratio (1:17). The research presents strong evidence that the surface fluidity and size of the aAPCs are critical to the effective formation of immune synapses essential for T cell activation. The findings demonstrate that the microfluidic-generated aAPCs can be instrumental in investigating the physiological conditions and mechanisms for T cell activation. Finally, this method demonstrates the feasibility of customizable aAPCs for a cost-effective off-the-shelf approach to immunotherapy.

Indexed as

Antigen-Presenting CellsLeukocytes, MononuclearImmunotherapyLipidsLymphocyte ActivationLipidsartificial antigen-presenting cellsdroplet generationimmunotherapymicrofluidicsT cell activation

Identifiers

PMID36645182
PMCPMC10175210
OpenAlexW4316469377

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.