Controlled release strategies for modulating immune responses to promote tissue regeneration
Journal of Controlled Release, ISSN: 0168-3659, Vol: 219, Page: 155-166
2015
- 38Citations
- 99Captures
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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
- Citations38
- Citation Indexes38
- 38
- CrossRef34
- Captures99
- Readers99
- 99
Article Description
Advances in the field of tissue engineering have enhanced the potential of regenerative medicine, yet the efficacy of these strategies remains incomplete, and is limited by the innate and adaptive immune responses. The immune response associated with injury or disease combined with that mounted to biomaterials, transplanted cells, proteins, and gene therapies vectors can contribute to the inability to fully restore tissue function. Blocking immune responses such as with anti-inflammatory or immunosuppressive agents are either ineffective, as the immune response contributes significantly to regeneration, or have significant side effects. This review describes targeted strategies to modulate the immune response in order to limit tissue damage following injury, promote an anti-inflammatory environment that leads to regeneration, and induce antigen (Ag)-specific tolerance that can target degenerative diseases that destroy tissues and promote engraftment of transplanted cells. Focusing on targeted immuno-modulation, we describe local delivery techniques to sites of inflammation as well as systemic approaches that preferentially target subsets of immune populations.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168365915300602; http://dx.doi.org/10.1016/j.jconrel.2015.08.014; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84947492634&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26264833; https://linkinghub.elsevier.com/retrieve/pii/S0168365915300602
Elsevier BV
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