Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms18081742
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dc.titleMarkers of T cell senescence in humans
dc.contributor.authorXu, W
dc.contributor.authorLarbi, A
dc.date.accessioned2020-09-14T08:02:35Z
dc.date.available2020-09-14T08:02:35Z
dc.date.issued2017
dc.identifier.citationXu, W, Larbi, A (2017). Markers of T cell senescence in humans. International Journal of Molecular Sciences 18 (8) : 1742. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms18081742
dc.identifier.issn1661-6596
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/176084
dc.description.abstractMany countries are facing the aging of their population, and many more will face a similar obstacle in the near future, which could be a burden to many healthcare systems. Increased susceptibility to infections, cardiovascular and neurodegenerative disease, cancer as well as reduced efficacy of vaccination are important matters for researchers in the field of aging. As older adults show higher prevalence for a variety of diseases, this also implies higher risk of complications, including nosocomial infections, slower recovery and sequels that may reduce the autonomy and overall quality of life of older adults. The age-related effects on the immune system termed as “immunosenescence” can be exemplified by the reported hypo-responsiveness to influenza vaccination of the elderly. T cells, which belong to the adaptive arm of the immune system, have been extensively studied and the knowledge gathered enables a better understanding of how the immune system may be affected after acute/chronic infections and how this matters in the long run. In this review, we will focus on T cells and discuss the surface and molecular markers that are associated with T cell senescence. We will also look at the implications that senescent T cells could have on human health and diseases. Finally, we will discuss the benefits of having these markers for investigators and the future work that is needed to advance the field of T cell senescence markers. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.
dc.sourceUnpaywall 20200831
dc.subjectCD27 antigen
dc.subjectCD28 antigen
dc.subjectCD45RA antigen
dc.subjectCD45RO antigen
dc.subjectCD57 antigen
dc.subjectchemokine receptor CCR7
dc.subjectgamma interferon
dc.subjectgranzyme B
dc.subjectinterleukin 2
dc.subjectinterleukin 4
dc.subjectinterleukin 5
dc.subjectnatural killer cell lectin like receptor
dc.subjectperforin
dc.subjectprotein p16
dc.subjectprotein p21
dc.subjecttelomerase reverse transcriptase
dc.subjecttranscription factor T bet
dc.subjecttumor necrosis factor
dc.subjectzinc finger protein
dc.subjectaging
dc.subjectcell assay
dc.subjectcell cycle
dc.subjectcell differentiation
dc.subjectcell function
dc.subjectcell proliferation
dc.subjectflow cytometry
dc.subjecthuman
dc.subjectimmunosenescence
dc.subjectmucosal-associated invariant T cell
dc.subjectnatural killer T cell
dc.subjectpersistent infection
dc.subjectphenotype
dc.subjectReview
dc.subjectsignal transduction
dc.subjectT lymphocyte
dc.subjectcell aging
dc.subjectcytology
dc.subjectimmunology
dc.subjectimmunophenotyping
dc.subjectprocedures
dc.subjectT lymphocyte
dc.subjectAging
dc.subjectCell Differentiation
dc.subjectCellular Senescence
dc.subjectHumans
dc.subjectImmunophenotyping
dc.subjectImmunosenescence
dc.subjectT-Lymphocytes
dc.typeReview
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.3390/ijms18081742
dc.description.sourcetitleInternational Journal of Molecular Sciences
dc.description.volume18
dc.description.issue8
dc.description.page1742
dc.published.statePublished
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