Role of dendritic cells in inflammation and loss of tolerance in the elderly
Frontiers in Immunology, ISSN: 1664-3224, Vol: 8, Issue: JUL, Page: 896
2017
- 110Citations
- 138Captures
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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
- Citations110
- Citation Indexes110
- 110
- CrossRef2
- Captures138
- Readers138
- 138
Review Description
Dendritic cells (DCs) play an important role in advancing age-associated progressive decline in adaptive immune responses, loss of tolerance, and development of chronic inflammation. In aged humans, DCs secrete increased levels of pro-inflammatory cytokines and decreased levels of anti-inflammatory and immune-regulatory cytokines. This may contribute to both chronic inflammation and loss of tolerance in aging. Aged DCs also display increased immune response against self-antigens contributing further to both inflammation and loss of tolerance. The secretion of innate protective cytokines such as type I and III interferons is decreased, and the function of DCs in airway remodeling and inflammation in aged is also compromised. Furthermore, the capacity of DCs to prime T cell responses also seems to be affected. Collectively, these changes in DC functions contribute to the immune dysfunction and inflammation in the elderly. This review only focuses on age-associated changes in DC function in humans.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85026498827&origin=inward; http://dx.doi.org/10.3389/fimmu.2017.00896; http://www.ncbi.nlm.nih.gov/pubmed/28798751; http://journal.frontiersin.org/article/10.3389/fimmu.2017.00896/full; https://dx.doi.org/10.3389/fimmu.2017.00896; https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2017.00896/full
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