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In vitro effects of dual wavelength photobiomodulation on monocytic response in painful temporomandibular disorder
1Division of Prosthodontics, Restorative Dental Sciences Department, University of Florida College of Dentistry, Gainesville, FL 32610, USA
2Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL 32610, USA
3Community Department of Community Dentistry and Behavioral Science, College of Dentistry, University of Florida, Gainesville, FL 32610, USA
4Pain Research and Intervention Center (PRICE), College of Dentistry, University of Florida, Gainesville, FL 32611, USA
5Department of Oral and Maxillofacial Diagnostic Sciences, University of Florida, Gainesville, FL 32610, USA
6Department of Oral Diagnostic Sciences, School of Dental Medicine, University at Buffalo, Buffalo, NY 14214, USA
DOI: 10.22514/jofph.2025.082 Vol.39,Issue 4,December 2025 pp.252-257
Submitted: 03 April 2025 Accepted: 06 June 2025
Published: 12 December 2025
*Corresponding Author(s): Margarete C. Ribeiro Dasilva E-mail: mribeiro@dental.ufl.edu
Temporomandibular disorders (TMD) are a prevalent source of chronic pain and disability, yet current therapies often provide limited relief with notable side effects. Photobiomodulation (PBM) has emerged as a promising non-pharmacologic approach to modulate inflammation and pain. This study investigated the effects of a dual-wavelength PBM protocol (laser + light-emitting diode (LED)) on the lipopolysaccharide (LPS)-stimulated monocyte response from individuals with painful TMD. Monocytes were isolated from 16 individuals with TMD enrolled in a randomized, placebo-controlled clinical trial (NCT05916235). Cells were plated into 96-well plates and divided into Control, LPS, and LPS + PBM treatment groups. Monocytes received four alternating-day treatments with two PBM probes: a laser probe (810/660 nm, 180 J/cm²) and an LED probe (660/850 nm). Cytokine and chemokine levels in culture supernatants were measured via multiplexed immunoassays. To verify cell viability after PBM treatment, the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was used. Statistical analysis was conducted using one-way analysis of variance (ANOVA) with Bonferroni correction, and p < 0.05 was considered significant. PBM significantly reduced levels of pro-inflammatory mediators interleukin-1 beta (IL-1β) (p = 0.005), C-X-C motif chemokine ligand 9 (CXCL9) (p = 0.0042), interferon gamma–induced protein 10 (IP-10) (p = 0.001), and tumor necrosis factor-alpha (TNF-α) (p = 0.0003), while increasing expression of regulatory mediators interleukin-10 (IL-10) (p = 0.0009), interleukin-1 receptor antagonist (IL-1RA) (p = 0.004), and CC motif chemokine ligand 17 (CCL17) (p = 0.003).These findings suggest that the dual-wavelength PBM protocol was able to shift the monocyte immune response from a more pro-inflammatory (M1) phenotype to a more anti-inflammatory, tissue-repair (M2) cytokine profile. These results provide additional evidence for PBM as a benign and non-invasive technique to control and potentially modify TMD-related inflammation. ClinicalTrials.gov ID: NCT05916235.
Temporomandibular disorder; Photobiomodulation; Monocytes; Cytokines; Inflammation
Maria Gabriela Rodriguez,Mathew Warchol,Selenia Rubio,Patricia Cabrera,Rory Reever,Sherif Hosney,Cesar A. Migliorati,Frank C. Gibson III,Richard Ohrbach,Roger B. Fillingim,Shannon Wallet,Margarete C. Ribeiro Dasilva. In vitro effects of dual wavelength photobiomodulation on monocytic response in painful temporomandibular disorder. Journal of Oral & Facial Pain and Headache. 2025. 39(4);252-257.
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