Evidence map›Paper›PMID 38648258›Full record

ArticleAdvanced healthcare materials2024

Conjugation of IL-33 to Microporous Annealed Particle Scaffolds Enhances Type 2-Like Immune Responses In Vitro and In Vivo.

Colleen A Roosa, Samantha L Lempke, Riley T Hannan, Ethan Nicklow, Jeffrey M Sturek, Sarah E Ewald, Donald R Griffin

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 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
2.2field-weighted citation impact, top 13% 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, 9 citations in OpenAlex.

  1. Article
  2. Review
  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

7 authors at 2 institutions in 1 country.

Colleen A RoosaDepartment of Biomedical Engineering, University of Virginia, 415 Lane Rd, Charlottesville, VA, 22903, USA.
Samantha L LempkeDepartment of Microbiology, Immunology, and Cancer Biology, Beirne B. Carter Immunology Center, University of Virginia, 200 Jeanette Lancaster Way, Charlottesville, VA, 22903, USA.
Riley T HannanDepartment of Medicine, Pulmonary and Critical Care, University of Virginia, 1221 Lee St, Charlottesville, VA, 22903, USA.
Ethan NicklowDepartment of Biomedical Engineering, University of Virginia, 415 Lane Rd, Charlottesville, VA, 22903, USA.
Jeffrey M SturekDepartment of Medicine, Pulmonary and Critical Care, University of Virginia, 1221 Lee St, Charlottesville, VA, 22903, USA.
Sarah E EwaldDepartment of Microbiology, Immunology, and Cancer Biology, Beirne B. Carter Immunology Center, University of Virginia, 200 Jeanette Lancaster Way, Charlottesville, VA, 22903, USA.
Donald R GriffinDepartment of Biomedical Engineering, University of Virginia, 415 Lane Rd, Charlottesville, VA, 22903, USA.ORCID 0000-0002-3458-867X
University of Virginia · USCarter Center · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Dina Gould Halme · 1987 to 2026
$72.1M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007496 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Michael G. Brown, Coleen A McNamara · 1995 to 2026
$10.2M
Biotechnology Training ProgramT32GM136615 · NIGMS · UNIVERSITY OF VIRGINIA · PI Silvia Salinas Blemker, Kimberly A. Kelly · 2020 to 2026
$3.4M
Improving Biomaterial Implant Tolerance with Damage-Associated Molecular Pathway (DAMP) Molecule AttachmentR21EB028971 · NIBIB · UNIVERSITY OF VIRGINIA · PI EWALD, SARAH E., GRIFFIN, DONALD RICHIERI · 2020 to 2022
$634k
Role of Natural Antibodies and B1 cells in Fibroproliferative Lung DiseaseF32HL170760 · NHLBI · UNIVERSITY OF VIRGINIA · PI HANNAN, RILEY T · 2023 to 2025
$150k
NCI NIH HHS P30 CA044579NCI NIH HHS P30-CA044579NHLBI NIH HHS F32 HL170760NIAID NIH HHS T32 AI007496NIBIB NIH HHS R21 EB028971NIBIB NIH HHS R21EB028971NIGMS NIH HHS T32 GM136615NIH HHS T32GM136615NIH T32 Immunology Training GrantUniversity of Virginia Dean's Scholars Fellowship
6 · The paper itself

Abstract

The inflammatory foreign body response (FBR) is the main driver of biomaterial implant failure. Current strategies to mitigate the onset of a FBR include modification of the implant surface, release of anti-inflammatory drugs, and cell-scale implant porosity. The microporous annealed particle (MAP) scaffold platform is an injectable, porous biomaterial composed of individual microgels, which are annealed in situ to provide a structurally stable scaffold with cell-scale microporosity. MAP scaffold does not induce a discernible foreign body response in vivo and, therefore, can be used a "blank canvas" for biomaterial-mediated immunomodulation. Damage associated molecular patterns (DAMPs), such as IL-33, are potent regulators of type 2 immunity that play an important role in tissue repair. In this manuscript, IL-33 is conjugated to the microgel building-blocks of MAP scaffold to generate a bioactive material (IL33-MAP) capable of stimulating macrophages in vitro via a ST-2 receptor dependent pathway and modulating immune cell recruitment to the implant site in vivo, which indicates an upregulation of a type 2-like immune response and downregulation of a type 1-like immune response.

Indexed as

Interleukin-33Tissue ScaffoldsAnimalsBiocompatible MaterialsForeign-Body ReactionHumansInterleukin-1 Receptor-Like 1 ProteinMacrophagesMiceMice, Inbred C57BLPorosityRAW 264.7 CellsBiocompatible MaterialsInterleukin-1 Receptor-Like 1 ProteinInterleukin-33foreign body responseimmunomodulationporous biomaterialstissue‐implant integration

Identifiers

PMID38648258
PMCPMC11461124
OpenAlexW4394995867

What OpenQuestion holds

Textmetadata
LicenceTDM
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.