Convergence of Innate and Adaptive Immunity during Human Aging
Aging is associated with profound changes in the human immune system, a phenomenon referred to as immunosenescence. This complex immune remodeling affects the adaptive immune system and the CD8 T cell compartment in particular, leading to the accumulation of terminally differentiated T cells, which...
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Published in | Frontiers in immunology Vol. 7; p. 445 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
04.11.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Aging is associated with profound changes in the human immune system, a phenomenon referred to as immunosenescence. This complex immune remodeling affects the adaptive immune system and the CD8
T cell compartment in particular, leading to the accumulation of terminally differentiated T cells, which can rapidly exert their effector functions at the expenses of a limited proliferative potential. In this review, we will discuss evidence suggesting that senescent αβCD8
T cells acquire the hallmarks of innate-like T cells and use recently acquired NK cell receptors as an alternative mechanism to mediate rapid effector functions. These cells concomitantly lose expression of co-stimulatory receptors and exhibit decreased T cell receptor signaling, suggesting a functional shift away from antigen-specific activation. The convergence of innate and adaptive features in senescent T cells challenges the classic division between innate and adaptive immune systems. Innate-like T cells are particularly important for stress and tumor surveillance, and we propose a new role for these cells in aging, where the acquisition of innate-like functions may represent a beneficial adaptation to an increased burden of malignancy with age, although it may also pose a higher risk of autoimmune disorders. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Reviewed by: Nan-ping Weng, National Institute on Aging, USA; Rafael Solana, University of Córdoba, Spain Specialty section: This article was submitted to T Cell Biology, a section of the journal Frontiers in Immunology Edited by: Fernando A. Arosa, University of Beira Interior, Portugal |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2016.00445 |