Control of innate immune response by biomaterial surface topography, energy, and stiffness
Open accessAbstract
As the focus of implantable biomaterials has shifted from bioinert implants to bioactive designs, recent research has highlighted the complex interactions between cell physiologic systems and material properties, particularly physical cues. From the cells known to interact with implanted biomaterials, the response of the immune system has been a critical target of study recently. Here, we review studies characterizing the response of innate immune cells to various material cues, particularly of those at the surface of implanted materials.The innate immune system consists of cell types with various roles in inflammation. Neutrophils and macrophages serve both phagocytic and signaling roles, especially early in the inflammatory phase of biomaterial implantation. These cell types ultimately dictate the outcome of implants as chronic inflammation, fibrosis, or integration. Other cell types like dendritic cells, mast cells, natural killer cells, and innate lymphoid cells may also serve an immunomodulatory role in the biomaterial context. This review highlights recent advances in our understanding of the role of innate immunity in the response to implantable biomaterials as well as key mechanobiological findings in innate immune cells underpinning these advances. STATEMENT OF SIGNIFICANCE: This review highlights recent advances in the understanding of the role of innate immunity in the response to implantable biomaterials, especially in neutrophils and macrophages, as well as key mechanobiological findings in innate immune cells underpinning these advances. Here we discuss how physicochemical properties of biomaterials control innate immune cell behavior.
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Macrophages are plastic and can dynamically shift phenotypes in response to environmental cues.
“An important feature of macrophages is their plasticity, the ability to dynamically shift phenotypes in response to environmental cues 10 .”
From Soft tissue-mimicking hydrogel stiffness modulates polarisation of human monocyte-derived macrophages (2025) · cites this paper as [10]
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References 248 · Cited by 199
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- Authors
- Abaricia, J. O., Farzad, N., Heath, T. J., Simmons, J., Morandini, L., & Olivares-Navarrete, R.
- Affiliations
- Virginia Commonwealth University (US)
- Venue
- Acta Biomaterialia
- Publisher
- Elsevier BV
- Published
- 2021-10
- Volume
- 133
- Pages
- 58-73
- ISSN
- 1742-7061 (ISSN-L)
- PMC
- PMC8497396
- OpenAlex
- W3156569796
- Cited by
- 199
- References
- 248
- Citations by year
- 2026: 36 · 2025: 46 · 2024: 46 · 2023: 37 · 2022: 28 · 2021: 6
- FWCI
- 2.50
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Acta Biomaterialia (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Dental and Craniofacial Research (R01DE028919)
- National Institutes of Health
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- innate immune response, implantable biomaterials, surface topography, mechanical energy, mechanobiology, neutrophils, macrophages, inflammation, fibrosis, biomaterial integration, physicochemical properties, dendritic cells, mast cells, natural killer cells, innate lymphoid cells
- MeSH terms
- Biocompatible Materials, Immunity, Innate, Lymphocytes, Macrophages, Prostheses and Implants
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