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Dental implant nanotopography for peri-implant tissue stability: soft-tissue sealing, innate immune calibration, and active biointerface regulation

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  • Published: 13 July 2026
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International Journal of Implant Dentistry Aims and scope Submit manuscript
Dental implant nanotopography for peri-implant tissue stability: soft-tissue sealing, innate immune calibration, and active biointerface regulation
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  • Takeru Kondo1,2,
  • Masahiro Yamada1,3,4,
  • Sara Ambo1 &
  • …
  • Hiroshi Egusa1,2,4,5 
  • 190 Accesses

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Abstract

Purpose

Peri-implantitis is a major biological complication in implant dentistry, associated with bacterial biofilm formation and amplified by dysregulated host immune responses. Increasing evidence indicates that implant and abutment surface properties influence not only osseointegration but also microbial retention, soft-tissue sealing, and innate immune cell behavior. This narrative review aimed to summarize the current evidence on how dental implant nanotopography may affect peri-implantitis-related biological responses, with particular emphasis on innate immunity, region-specific peri-implant biointerfaces, and peri-implant tissue stability.

Methods

Clinical, animal, and in vitro studies were reviewed to examine the pathogenesis of peri-implantitis, the roles of innate immune cells, the influence of implant and abutment surface topography on microbial and immune responses, and emerging nano-enabled strategies for the active regulation of peri-implant tissue responses.

Results

Peri-implantitis progression is shaped by the interplay among the disruption of transmucosal soft-tissue sealing, microbial invasion, implant- or abutment-derived foreign-body stimuli, and sustained dysregulated innate immune activation. Nanotopographic surfaces regulate epithelial and fibroblastic attachment, extracellular matrix organization, neutrophil and macrophage responses, and osteocyte network formation via mechanotransduction. The biological effects of nanotopography are design-dependent and are influenced by nanoscale geometry, size, hydrophilicity, and associated physicochemical properties, including surface chemistry, wettability, and charge. Additionally, anisotropic nanospike surfaces and nano-enabled biomolecule delivery technologies illustrate the future possibility of active nanointerface regulation beyond conventional surface modification, although intracellular delivery technologies currently remain conceptual for dental implant applications.

Conclusions

Implant and abutment nanotopography may contribute to peri-implant tissue stability by coordinating soft-tissue sealing, microbial retention control, innate immune calibration, and bone-interface resilience. Although direct clinical evidence remains limited, region-specific and functionally active nano-biointerfaces may offer new opportunities to reduce susceptibility to peri-implant inflammatory tissue breakdown.

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Acknowledgements

This study was supported by Grants-in-Aid from the Japan Society for Scientific Research (B: 24K02625, M.Y. and H.E.) and the Promotion of Science Research Fellowship for Early-Career Scientists (25K20340, T.K.).

Funding

This study was supported by Grants-in-Aid from the Japan Society for Scientific Research (B: 24K02625, M.Y. and H.E.) and the Promotion of Science Research Fellowship for Early-Career Scientists (25K20340, T.K.).

Author information

Authors and Affiliations

  1. Division of Molecular and Regenerative Prosthodontics, Tohoku University Graduate School of Dentistry, Sendai, Miyagi, Japan

    Takeru Kondo, Masahiro Yamada, Sara Ambo & Hiroshi Egusa

  2. Division of Next-Generation Dental Material Engineering, Tohoku University Graduate School of Dentistry, Sendai, Miyagi, Japan

    Takeru Kondo & Hiroshi Egusa

  3. Division of Mechanobiology and Biomedical-Dental Engineering, Tohoku University Graduate School of Biomedical Engineering, Sendai, Miyagi, Japan

    Masahiro Yamada

  4. Centre of Excellence for Dental Stem Cell Biology, Faculty of Dentistry, Chulalongkorn University, Pathumwan, Bangkok, Thailand

    Masahiro Yamada & Hiroshi Egusa

  5. Center for Advanced Stem Cell and Regenerative Research, Tohoku University Graduate School of Dentistry, Sendai, Miyagi, Japan

    Hiroshi Egusa

Authors
  1. Takeru Kondo
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  2. Masahiro Yamada
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  3. Sara Ambo
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  4. Hiroshi Egusa
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Corresponding authors

Correspondence to Masahiro Yamada or Hiroshi Egusa.

Ethics declarations

Ethics approval and consent to participate

Not applicable. This narrative review did not involve human participants, human data, human tissue, or animal experiments. Therefore, approval from an ethics committee or Institutional Review Board was not required.

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Not applicable.

Competing interests

The authors declare no competing interests.

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Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Cite this article

Kondo, T., Yamada, M., Ambo, S. et al. Dental implant nanotopography for peri-implant tissue stability: soft-tissue sealing, innate immune calibration, and active biointerface regulation. Int J Implant Dent (2026). https://doi.org/10.1186/s40729-026-00703-4

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  • Received: 08 June 2026

  • Accepted: 07 July 2026

  • Published: 13 July 2026

  • DOI: https://doi.org/10.1186/s40729-026-00703-4

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Keywords

  • Dental implant
  • Peri-implantitis
  • Nanotopography
  • Innate immunity
  • Mechanotransduction
  • Soft-tissue sealing

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