Chronic inflammation in immune aging: role of pattern recognition receptor crosstalk with the telomere complex?
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F17%3A00067117" target="_blank" >RIV/00159816:_____/17:00067117 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/17:00099687 RIV/65269705:_____/17:00067117
Result on the web
<a href="http://journal.frontiersin.org/article/10.3389/fimmu.2017.01078/abstract" target="_blank" >http://journal.frontiersin.org/article/10.3389/fimmu.2017.01078/abstract</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fimmu.2017.01078" target="_blank" >10.3389/fimmu.2017.01078</a>
Alternative languages
Result language
angličtina
Original language name
Chronic inflammation in immune aging: role of pattern recognition receptor crosstalk with the telomere complex?
Original language description
Age-related decline in immunity is characterized by stem cell exhaustion, telomere shortening, and disruption of cell-to-cell communication, leading to increased patient risk of disease. Recent data have demonstrated that chronic inflammation exerts a strong influence on immune aging and is closely correlated with telomere length in a range of major pathologies. The current review discusses the impact of inflammation on immune aging, the likely molecular mediators of this process, and the various disease states that have been linked with immunosenescence. Emerging findings implicate NFkB, the major driver of inflammatory signaling, in several processes that regulate telomere maintenance and/or telomerase activity. While prolonged triggering of pattern recognition receptors is now known to promote immunosenescence, it remains unclear how this process is linked with the telomere complex or telomerase activity. Indeed, enzymatic control of telomere length has been studied for many decades, but alternative roles of telomerase and potential influences on inflammatory responses are only now beginning to emerge. Crosstalk between these pathways may prove to be a key molecular mechanism of immunosenescence. Understanding how components of immune aging interact and modify host protection against pathogens and tumors will be essential for the design of new vaccines and therapies for a wide range of clinical scenarios.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Frontiers in Immunology
ISSN
1664-3224
e-ISSN
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Volume of the periodical
8
Issue of the periodical within the volume
SEP
Country of publishing house
CH - SWITZERLAND
Number of pages
10
Pages from-to
1078
UT code for WoS article
000409062200001
EID of the result in the Scopus database
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