Evidence map›Paper›PMID 30075952›Full record

ArticleBiomaterials2019

Controlled M1-to-M2 transition of aged macrophages by calcium phosphate coatings.

Jumana R Alhamdi, Tao Peng, Iman M Al-Naggar, Kelly L Hawley, Kara L Spiller, Liisa T Kuhn

Abstract read
In one paragraph

Article in Biomaterials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
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  5. Affinity-based controlled release of interleukin-4 from scaffolds via biotin-streptavidin interactions for immunomodulation.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  6. Review
  7. Review
  8. TiAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Review
  10. Article
  11. Understanding the properties of intermittent catheters to inform future development.Proceedings of the Institution of Mechanical Engineers. Part H, Journal of engineering in medicine · 2024
    Review
  12. Review
  13. Review
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  15. Article
  16. A new osteogenic protein isolated fromBioactive materials · 2023
    Article
  17. Review
  18. Article
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  20. Review
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.

Jumana R AlhamdiBiomedical Engineering, University of Connecticut (UConn) Health, Farmington, CT, USA.
Tao PengBiomedical Engineering, University of Connecticut (UConn) Health, Farmington, CT, USA.
Iman M Al-NaggarCenter on Aging, University of Connecticut (UConn) Health, Farmington, CT, USA.
Kelly L HawleyDepartment of Pediatrics, University of Connecticut (UConn) Health, Farmington, CT, USA; Division of Infectious Diseases, Connecticut Children's Medical Center, Hartford, CT, USA.
Kara L SpillerSchool of Biomedical Engineering, Science and Health Systems, Drexel University, PA, USA.
Liisa T KuhnBiomedical Engineering, University of Connecticut (UConn) Health, Farmington, CT, USA. Electronic address: lkuhn@uchc.edu.

Funding

Understanding and Controlling Macrophage Behavior in AngiogenesisR01HL130037 · NHLBI · DREXEL UNIVERSITY · PI SPILLER, KARA LORRAINE · 2016 to 2024
$4.7M
Modulated release of growth factors for stimulating progenitors in aging boneR01DE021103 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KUHN, LIISA TIINA · 2012 to 2025
$4.4M
NHLBI NIH HHS R01 HL130037NIDCR NIH HHS R01 DE021103
6 · The paper itself

Abstract

Older adults suffer from weakened and delayed bone healing due to age-related alterations in bone cells and in the immune system. Given the interaction between the immune system and skeletal cells, therapies that address deficiencies in both the skeletal and the immune system are required to effectively treat bone injuries of older patients. The sequence of macrophage activation observed in healthy tissue repair involves a transition from a pro-inflammatory state followed by a pro-reparative state. In older patients, inflammation is slower to resolve and impedes healing. The goal of this study was to design a novel drug delivery system for temporal guidance of the polarization of macrophages using bone grafting materials. A biomimetic calcium phosphate coating (bCaP) physically and temporally separated the pro-inflammatory stimulus interferon-gamma (IFNγ) from the pro-reparative stimulus simvastatin (SIMV). Effective doses were identified using a human monocyte line (THP-1) and testing culminated with bone marrow macrophages obtained from old mice. Sequential M1-to-M2 activation was achieved with both cell types. These results suggest that this novel immunomodulatory drug delivery system holds potential for controlling macrophage activation in bones of older patients.

Indexed as

Cellular SenescenceAnimalsCalcium PhosphatesCoated Materials, BiocompatibleDose-Response Relationship, DrugDrug Delivery SystemsGene Expression RegulationHumansInterferon-gammaKineticsMacrophagesMaleMice, Inbred C57BLSimvastatinTHP-1 CellsTime Factorscalcium phosphateCalcium PhosphatesCoated Materials, BiocompatibleInterferon-gammaSimvastatinAgingBone repairCalcium phosphateDrug deliveryMacrophagesSimvastatin

Identifiers

PMID30075952
PMCPMC6336526

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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.