Evidence map›Paper›PMID 38739450›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2024

Shape-Versatile Fixed Cellular Materials for Multiple Target Immunomodulation.

Ana Rita Sousa, Ana F Cunha, Ana Santos-Coquillat, Beatriz Hernaez Estrada, Kara L Spiller, Marta Barão, Artur Filipe Rodrigues, Susana Simões, Andreia Vilaça, Lino Ferreira and 2 more

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2024. 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
–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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

12 authors.

Ana Rita SousaDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal.
Ana F CunhaDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal.ORCID 0000-0001-9562-2707
Ana Santos-CoquillatDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal.
Beatriz Hernaez EstradaSchool of Biomedical Engineering, Science, and Health Systems, Drexel University, 3141 Chestnut Street, Philadelphia, PA, 19104, USA.
Kara L SpillerSchool of Biomedical Engineering, Science, and Health Systems, Drexel University, 3141 Chestnut Street, Philadelphia, PA, 19104, USA.
Marta BarãoCNC-Center for Neurosciences and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, 3004-517, Portugal.
Artur Filipe RodriguesCNC-Center for Neurosciences and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, 3004-517, Portugal.
Susana SimõesCNC-Center for Neurosciences and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, 3004-517, Portugal.
Andreia VilaçaCNC-Center for Neurosciences and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, 3004-517, Portugal.
Lino FerreiraCNC-Center for Neurosciences and Cell Biology, CIBB-Center for Innovative Biomedicine and Biotechnology, University of Coimbra, Coimbra, 3004-517, Portugal.
Mariana B OliveiraDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal.ORCID 0000-0002-6104-6075
João F ManoDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal.ORCID 0000-0002-2342-3765

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Claudio Guillermo Giraudo · 1995 to 2026
$94.8M
Understanding and Controlling Macrophage Behavior in AngiogenesisR01HL130037 · NHLBI · DREXEL UNIVERSITY · PI SPILLER, KARA LORRAINE · 2016 to 2024
$4.7M
COMPETE2020 and PRR project "Agenda/Alianças mobilizadoras para a reindustrilização C630926586-00465198Division of Cancer Prevention, National Cancer Institute P30CA056036-17Fundação para a Ciência e a Tecnologia LA/P/0006/2020Fundação para a Ciência e a Tecnologia UIDB/50011/2020Fundação para a Ciência e a Tecnologia UIDP/50011/2020National funds (OE) through FCT/MCTES, in the scope of the project PTDC/BTM-ORG/3215/2020(doi.org/10.54499/PTDC/BTM-ORG/3215/2020)National funds through the FCT/MCTES (PIDDAC) 2021.04817.BD(doi.org/10.54499/2021.04817.BD)National funds through the FCT/MCTES (PIDDAC) 2023/0222National funds through the FCT/MCTES (PIDDAC) SFRH/BD/145765/2019NCI NIH HHS P30 CA056036NHLBI NIH HHS R01 HL130037NHLBI NIH HHS R01HL130037"Prova de conceito" project with the acronym "Bio-Med" 181228PRR through the project HfPT-Health from Portugal 02/C05-i01.01/2022.PC644937233-00000047Scientific Employment Stimulus - Institutional Call CEECINST/00013/2021(doi.org/10.54499/CEECINST/00013/2021/CP2779/CT0010)
6 · The paper itself

Abstract

Therapeutic cells are usually administered as living agents, despite the risks of undesired cell migration and acquisition of unpredictable phenotypes. Additionally, most cell-based therapies rely on the administration of single cells, often associated with rapid in vivo clearance. 3D cellular materials may be useful to prolong the effect of cellular therapies and offer the possibility of creating structural volumetric constructs. Here, the manufacturing of shape-versatile fixed cell-based materials with immunomodulatory properties is reported. Living cell aggregates with different shapes (spheres and centimeter-long fibers) are fixed using a method compatible with maintenance of structural integrity, robustness, and flexibility of 3D constructs. The biological properties of living cells can be modulated before fixation, rendering an in vitro anti-inflammatory effect toward human macrophages, in line with a decreased activation of the nuclear factor kappa B (NF-κB) pathway that preponderantly correlated with the surface area of the materials. These findings are further corroborated in vivo in mouse skin wounds. Contact with fixed materials also reduces the proliferation of activated primary T lymphocytes, while promoting regulatory populations. The fixation of cellular constructs is proposed as a versatile phenotypic stabilization method that can be easily implemented to prepare immunomodulatory materials with therapeutic potential.

Indexed as

ImmunomodulationAnimalsCell ProliferationHumansMacrophagesMiceNF-kappa BT-LymphocytesWound HealingNF-kappa Bcellular materialsfixed cell‐rich materialsimmunomodulationimmunosuppressionshape‐adaptability

Identifiers

PMID38739450
PMCPMC11272431

What OpenQuestion holds

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Registered trials

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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.