Evidence map›Paper›PMID 39000385›Full record

ReviewInternational journal of molecular sciences2024

Targeting Macrophage Polarization for Reinstating Homeostasis following Tissue Damage.

Qiran Du, Anna Dickinson, Pruthvi Nakuleswaran, Susan Maghami, Savindu Alagoda, Andrew L Hook, Amir M Ghaemmaghami

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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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

7 authors.

Qiran DuImmuno-Bioengineering Group, School of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0009-0005-3034-6699
Anna DickinsonMedical School, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Pruthvi NakuleswaranMedical School, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Susan MaghamiHull York Medical School, University of York, York YO10 5DD, UK.
Savindu AlagodaMedical School, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0009-0009-7914-6662
Andrew L HookSchool of Pharmacy, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0001-7756-8444
Amir M GhaemmaghamiImmuno-Bioengineering Group, School of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0003-3160-8759

Funding

Engineering and Physical Sciences Research Council (EPSRC) EP/X001156/1Engineering and Physical Sciences Research Council (EPSRC) EP/Y002423/1
6 · The paper itself

Abstract

Tissue regeneration and remodeling involve many complex stages. Macrophages are critical in maintaining micro-environmental homeostasis by regulating inflammation and orchestrating wound healing. They display high plasticity in response to various stimuli, showing a spectrum of functional phenotypes that vary from M1 (pro-inflammatory) to M2 (anti-inflammatory) macrophages. While transient inflammation is an essential trigger for tissue healing following an injury, sustained inflammation (e.g., in foreign body response to implants, diabetes or inflammatory diseases) can hinder tissue healing and cause tissue damage. Modulating macrophage polarization has emerged as an effective strategy for enhancing immune-mediated tissue regeneration and promoting better integration of implantable materials in the host. This article provides an overview of macrophages' functional properties followed by discussing different strategies for modulating macrophage polarization. Advances in the use of synthetic and natural biomaterials to fabricate immune-modulatory materials are highlighted. This reveals that the development and clinical application of more effective immunomodulatory systems targeting macrophage polarization under pathological conditions will be driven by a detailed understanding of the factors that regulate macrophage polarization and biological function in order to optimize existing methods and generate novel strategies to control cell phenotype.

Indexed as

HomeostasisMacrophagesWound HealingAnimalsBiocompatible MaterialsHumansInflammationMacrophage ActivationBiocompatible Materialsbiomaterialsimmune-instructive materialsimmune modulationinflammationmacrophage polarizationmedical devicestissue repair

Identifiers

PMID39000385
PMCPMC11242417

What Socratic 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 Socratic graph.