Evidence map›Paper›PMID 35090200›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2022

Macrophage activation in response to shape memory polymer foam-coated aneurysm occlusion devices.

Sarah M Chau, Scott M Herting, Dillon A Noltensmeyer, Hamzah Ahmed, Duncan J Maitland, Shreya Raghavan

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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 2 institutions in 1 country.

Sarah M ChauDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Scott M HertingDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Dillon A NoltensmeyerDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Hamzah AhmedDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Duncan J MaitlandDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.
Shreya RaghavanDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA.ORCID 0000-0002-4631-7762
Texas A&M University · USHouston Methodist · US

Funding

Shape Memory Polymer Embolic Foams for Treating Cerebrovascular AneurysmsU01NS089692 · NINDS · TEXAS ENGINEERING EXPERIMENT STATION · PI MAITLAND, DUNCAN J · 2015 to 2018
$2.5M
National Defense Science and Engineering Graduate (NDSEG) Fellowship Program (SMH)NINDS NIH HHS U01 NS089692Texas A&M Engineering Experiment Station and the Department of Biomedical Engineering (SR)
6 · The paper itself

Abstract

Brain aneurysms can be treated with embolic coils using minimally invasive approaches. It is advantageous to modulate the biologic response of platinum embolic coils. Our previous studies demonstrated that shape memory polymer (SMP) foam coated embolization coils (FCC) devices demonstrate enhanced healing responses in animal models compared with standard bare platinum coil (BPC) devices. Macrophages are the most prevalent immune cell type that coordinate the greater immune response to implanted materials. Hence, we hypothesized that the highly porous SMP foam coatings on embolic coils activate a pro-regenerative healing phenotype. To test this hypothesis, we analyzed the number and type of infiltrating macrophages in FCC or BPC devices implanted in a rabbit elastase aneurysm model. FCC devices elicited a great number of infiltration macrophages, skewed significantly to a pro-regenerative M2-like phenotype 90 days following implantation. We devised an in vitro assay, where monocyte-derived macrophages were placed in close association with FCC or BPC devices for 6-72 h. Macrophages encountering SMP FCC-devices demonstrated highly mixed activation phenotypes at 6 h, heavily skewing toward an M2-like phenotype by 72 h, compared with macrophages encountering BPC devices. Macrophage activation was evaluated using gene expression analysis, and secreted cytokine evaluation. Together, our results demonstrate that FCC devices promoted a pro-regenerative macrophage activation phenotype, compared with BPC devices. Our in vitro findings corroborate with in vivo observations that SMP-based modification of embolic coils can promote better healing of the aneurysm site, by sustaining a pro-healing macrophage phenotype.

Indexed as

Embolization, TherapeuticIntracranial AneurysmSmart MaterialsAnimalsBlood Vessel ProsthesisMacrophage ActivationPlatinumRabbitsPlatinumSmart Materialsbiomaterialsimmune responseimplantable materialsmacrophagesshape memory polymers

Identifiers

PMID35090200
PMCPMC9106830
OpenAlexW4210533045

What OpenQuestion holds

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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.