Single-cell analysis of peri-implant gingival tissue to assess implant biocompatibility and immune response.

Implant biocompatibility Peri-implantitis Polymorphonuclear neutrophils (PMNs) Screening platform Titanium

Journal

Journal of prosthodontic research
ISSN: 2212-4632
Titre abrégé: J Prosthodont Res
Pays: Japan
ID NLM: 101490359

Informations de publication

Date de publication:
03 Sep 2024
Historique:
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 4 9 2024
Statut: aheadofprint

Résumé

The innate immune response, particularly the reaction of polymorphonuclear neutrophils (PMNs), is crucial in shaping the outcomes of chronic inflammation, fibrosis, or osseointegration following biomaterial implantation. Peri-implantitis or peri-mucositis, inflammatory conditions linked to dental implants, pose a significant threat to implant success. We developed a single-cell analysis approach using a murine model to assess the immune response to implant materials, offering a practical screening tool for potential dental implants. We performed bioinformatics analysis and established a peri-implant inflammation model by inserting two titanium implants into the maxillary region, to examine the immune response. Bioinformatics analysis revealed that titanium implants triggered a host immune response, primarily mediated by PMNs. In the in vivo experiments, we observed a rapid PMN-mediated response, with increased infiltration around the implants and on the implant surface by day 3. Remarkably, PMN attachment to the implants persisted for 7 days, resembling the immune profiles seen in human implant-mediated inflammation. Our findings indicate that persistent attachment of the short-living PMNs to titanium implants can serve as an indicator or traits of peri-implant inflammation. Therefore, analyzing gingival tissue at the single-cell level could be a useful tool for evaluating the biocompatibility of candidate dental implants.

Identifiants

pubmed: 39231696
doi: 10.2186/jpr.JPR_D_23_00309
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Li-Tzu Wang (LT)

School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Ph.D. Program in Medical Biotechnology, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.

Sin-Ei Juang (SE)

Department of Anesthesiology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan.

Hsuan-Hao Chang (HH)

Department of Dentistry, National Taiwan University Hospital & Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.

Ai-Chia He (AC)

Department of Dentistry, National Taiwan University Hospital & Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.

Wei-An Chen (WA)

Department of Dentistry, National Taiwan University Hospital & Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.

Yu-Wen Huang (YW)

Department of Medical Research, National Taiwan University Hospital, Taipei, Taiwan.

Thomas E Van Dyke (TE)

Center for Clinical and Translational Research, Forsyth Institute, Cambridge, USA.
Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, USA.

Kevin Sheng-Kai Ma (KS)

Center for Global Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Department of Orthodontics and Dentofacial Orthopedics, Henry M. Goldman School of Dental Medicine, Boston University, Boston, USA.

Yi-Wen Chen (YW)

Department of Dentistry, National Taiwan University Hospital & Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.
Graduate Institute of Oral Biology, School of Dentistry, National Taiwan University, Taipei, Taiwan.

Classifications MeSH