Evidence map›Paper›PMID 39285613›Full record

ArticleACS applied materials & interfaces2024

3D Printing as a Strategy to Scale-Up Biohybrid Hydrogels for T Cell Manufacture.

Eduardo Pérez Del Río, Sergi Rey-Vinolas, Fabião Santos, Miquel Castellote-Borrell, Francesca Merlina, Jaume Veciana, Imma Ratera, Miguel A Mateos-Timoneda, Elisabeth Engel, Judith Guasch

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. 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
–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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
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

10 authors.

Eduardo Pérez Del RíoDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.
Sergi Rey-VinolasIMEM-BRT Group, Department of Materials Science and Engineering, EEBE, Technical University of Catalonia (UPC), Barcelona 08019, Spain.
Fabião SantosDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.
Miquel Castellote-BorrellDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.
Francesca MerlinaDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.
Jaume VecianaDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.ORCID 0000-0003-1023-9923
Imma RateraDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.ORCID 0000-0002-1464-9789
Miguel A Mateos-TimonedaBioengineering Institute of Technology, Universitat Internacional de Catalunya (UIC), Sant Cugat del Vallès 08195, Spain.ORCID 0000-0001-7657-1414
Elisabeth EngelCentro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Madrid 28029, Spain.ORCID 0000-0003-4855-8874
Judith GuaschDepartment of Molecular Nanoscience and Organic Materials, Institut de Ciència de Materials de Barcelona (CSIC), Campus UAB, Bellaterra 08193, Spain.ORCID 0000-0002-3571-4711

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of cellular immunotherapy treatments is introducing more efficient strategies to combat cancer as well as autoimmune and infectious diseases. However, the cellular manufacturing procedures associated with these therapies remain costly and time-consuming, thus limiting their applicability. Recently, lymph-node-inspired PEG-heparin hydrogels have been demonstrated to improve primary human T cell culture at the laboratory scale. To go one step further in their clinical applicability, we assessed their scalability, which was successfully achieved by 3D printing. Thus, we were able to improve primary human T cell infiltration in the biohybrid PEG-heparin hydrogels, as well as increase nutrient, waste, and gas transport, resulting in higher primary human T cell proliferation rates while maintaining the phenotype. Thus, we moved one step further toward meeting the requirements needed to improve the manufacture of the cellular products used in cellular immunotherapies.

Indexed as

HydrogelsPolyethylene GlycolsPrinting, Three-DimensionalT-LymphocytesCell ProliferationCells, CulturedHeparinHumansHeparinHydrogelsPolyethylene Glycols3D hydrogels3D printingcancercell therapyT cells

Identifiers

PMID39285613
PMCPMC11440455

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.