MicroRNA-mediated immune modulation as a therapeutic strategy in host-implant integration
Advanced Drug Delivery Reviews, ISSN: 0169-409X, Vol: 88, Page: 92-107
2015
- 18Citations
- 66Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations18
- Citation Indexes18
- 18
- CrossRef17
- Captures66
- Readers66
- 66
Review Description
The concept of implanting an artificial device into the human body was once the preserve of science fiction, yet this approach is now often used to replace lost or damaged biological structures in human patients. However, assimilation of medical devices into host tissues is a complex process, and successful implant integration into patients is far from certain. The body's immediate response to a foreign object is immune-mediated reaction, hence there has been extensive research into biomaterials that can reduce or even ablate anti-implant immune responses. There have also been attempts to embed or coat anti-inflammatory drugs and pro-regulatory molecules onto medical devices with the aim of preventing implant rejection by the host. In this review, we summarize the key immune mediators of medical implant reaction, and we evaluate the potential of microRNAs to regulate these processes to promote wound healing, and prolong host-implant integration.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0169409X15001088; http://dx.doi.org/10.1016/j.addr.2015.05.013; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84937517845&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26024977; https://linkinghub.elsevier.com/retrieve/pii/S0169409X15001088; https://dx.doi.org/10.1016/j.addr.2015.05.013
Elsevier BV
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