Evidence map›Paper›PMID 41649722›Full record

ArticleProgress in orthodontics2026

Orthodontic derived microplastics impact macrophage differentiation and homeostasis.

Jordan Warunek, Stephen Warunek, Michael Calderon, Jonathan Franks, Simon Watkins, Heth Turnquist, Thikriat Al-Jewair

Abstract read
In one paragraph

Article in Progress in orthodontics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. 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.

Jordan WarunekThomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, USA.
Stephen WarunekDepartment of Orthodontics, University at Buffalo, State University of New York, Buffalo, USA.
Michael CalderonDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, USA.
Jonathan FranksDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, USA.
Simon WatkinsDepartment of Cell Biology, University of Pittsburgh, Pittsburgh, USA.
Heth TurnquistThomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, USA.
Thikriat Al-JewairDepartment of Orthodontics, University at Buffalo, State University of New York, Buffalo, USA. thikriat@buffalo.edu.

Funding

Interdisciplinary Training in Transplantation BiologyT32AI074490 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Angus W Thomson · 2007 to 2026
$4.2M
Defining How Macrophage Allorecognition Impacts Tissue Repair After TransplantationF31HL170514 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WARUNEK, JORDAN · 2023 to 2025
$146k
National Institutes of Health (NIH) 5T32AI074490 and F31HL170514National Institutes of Health (NIH) R01HL22489NHLBI NIH HHS F31 HL170514NIAID NIH HHS T32 AI074490
6 · The paper itself

Abstract

backgroundSynthetic polymers are widely used in medical and dental appliances, including clear aligners, retainers, splints, and sleep devices. Despite their widespread use, little is known about the release of microplastics from traditional thermoformed polymers compared with recently developed direct-printed photopolymers. Plastic particles have been detected in a variety of human tissues such as, lung, liver, spleen and kidneys. Each of these sites contain local resident macrophages tasked with maintaining homeostasis by clearing cell debris and foreign bodies. Like these organs, the oral cavity has an extensive population of macrophages that complete immune surveillance and support oral tissue health. Therefore, orthodontic plastic particles may have profound local and systemic biological impacts. As such, we systematically characterized release and particle structure of several clinical orthodontic polymers and visualized their uptake and impacts on macrophage differentiation.

methodsPolymers were tested with the following compositions, direct-printed resins: ActiveMemory™ DCA (Lux Creo Inc.), Tera Harz TA-28 (Graphy Inc.), Nylon 12 (EOS) and thermoformed materials: Invisacryl™ (Great Lakes Dental Technologies), Zendura

resultsAll materials released detectable particles, with direct-printed polymers producing the highest concentrations. Direct-printed materials shed more micro-sized plastics, whereas thermoformed materials predominantly released nano-sized particles. Macrophages readily phagocytosed plastics about 2-10 μm in size. Co-culture with urethane-based direct-printed materials promoted macrophage differentiation toward M1-like iNOS⁺CD86⁺ subsets associated with pro-inflammatory activity.

conclusionsOur findings reveal that commonly used orthodontic materials release micro- and nano-plastics that are readily taken up by macrophages, with direct-printed polymers releasing higher levels of immunostimulatory particles. The resulting shift toward pro-inflammatory macrophage phenotypes raises concern that material choice could influence not only local oral health but also systemic immune responses. These results underscore the importance of evaluating microplastic release in dental and medical devices to guide safer material selection and minimize unintended biological consequences.

Indexed as

Cell DifferentiationHomeostasisMacrophagesMicroplasticsOrthodontic AppliancesAnimalsHumansPolymersMicroplasticsPolymersAligner applianceFlow cytometryMacrophageMicroplasticNanoplastic

Identifiers

PMID41649722
PMCPMC12881249

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.