Evidence map›Paper›PMID 37539029›Full record

ArticleiScience2023

Engineering a versatile and retrievable cell macroencapsulation device for the delivery of therapeutic proteins.

Julien Grogg, Remi Vernet, Emily Charrier, Muriel Urwyler, Olivier Von Rohr, Valentin Saingier, Fabien Courtout, Aurelien Lathuiliere, Nicolas Gaudenzio, Adrien Engel and 1 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

11 authors at 2 institutions in 2 countries.

Julien GroggDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Remi VernetDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Emily CharrierDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Muriel UrwylerDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Olivier Von RohrDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Valentin SaingierDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Fabien CourtoutDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Aurelien LathuiliereDepartment of Rehabilitation and Geriatrics, University of Geneva, 1211 Geneva, Switzerland.
Nicolas GaudenzioToulouse Institute for Infectious and Inflammatory Diseases (Infinity) INSERM UMR1291 - CNRS UMR5051 - University Toulouse III, Toulouse, France.
Adrien EngelDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
Nicolas MachDepartment of Oncology, Geneva University Hospitals and Medical School, 1211 Geneva, Switzerland.
University of Geneva · CHCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Encapsulated cell therapy holds a great potential to deliver sustained levels of highly potent therapeutic proteins to patients and improve chronic disease management. A versatile encapsulation device that is biocompatible, scalable, and easy to administer, retrieve, or replace has yet to be validated for clinical applications. Here, we report on a cargo-agnostic, macroencapsulation device with optimized features for protein delivery. It is compatible with adherent and suspension cells, and can be administered and retrieved without burdensome surgical procedures. We characterized its biocompatibility and showed that different cell lines producing different therapeutic proteins can be combined in the device. We demonstrated the ability of cytokine-secreting cells encapsulated in our device and implanted in human skin to mobilize and activate antigen-presenting cells, which could potentially serve as an effective adjuvant strategy in cancer immunization therapies. We believe that our device may contribute to cell therapies for cancer, metabolic disorders, and protein-deficient diseases.

Indexed as

Natural sciencesPharmaceutical sciencePharmacology

Identifiers

PMID37539029
PMCPMC10393802
OpenAlexW4384008718

What Socratic 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 Socratic graph.