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      The impact of ageing on natural killer cell function and potential consequences for health in older adults

      review-article
      * ,
      Ageing Research Reviews
      Elsevier Science
      ADCC, antibody dependent cell cytotoxicity, Apaf-1, apoptosis-activating factor 1, BID, BH3-interacting domain, CAD, caspase-activated DNase, CMV, cytomegalovirus, DC, dendritic cell, DLN, draining lymph node, FasL, Fas ligand, FADD, Fas-associated protein with death domain, iCAD, inhibitor of caspase-activated DNase, IFN-γ, interferon gamma, IL-8, interleukin 8, KIR, killer cell immunoglobulin like receptor, MHC, major histocompatibility complex, MIC, MHC class I-chain-related protein, MIP-1α, macrophage inflammatory protein-1-alpha, NCR, natural cytotoxicity receptor, NK cell, natural killer cell, NKCC, natural killer cell cytotoxicity, PARP, poly ADPribose polymerase, PBLs, peripheral blood lymphocytes, PMA, phorbol 12-myristate 13-acetate, TB, Mycobacterium tuberculosis, tBID, truncated BH3-interacting domain, TNF-α, tumour necrosis factor alpha, Th-1, T helper 1 cell, TRAIL, tumor necrosis factor related apoptotic-inducing ligand, Natural killer (NK) cells, Ageing, Immunesenescence

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          Highlights

          • Roles are emerging for natural killer (NK) cells beyond removing transformed cells.

          • These include immune regulation and the elimination of senescent cells.

          • Human ageing is associated with a decline in NK cell function.

          • We propose some aspects of human ageing are due in part to reduced NK cell function.

          • These include reduced vaccination efficacy and delayed resolution of inflammation.

          Abstract

          Forming the first line of defence against virally infected and malignant cells, natural killer (NK) cells are critical effector cells of the innate immune system. With age, significant impairments have been reported in the two main mechanisms by which NK cells confer host protection: direct cytotoxicity and the secretion of immunoregulatory cytokines and chemokines. In elderly subjects, decreased NK cell activity has been shown to be associated with an increased incidence and severity of viral infection, highlighting the clinical implications that age-associated changes in NK cell biology have on the health of older adults. However, is an increased susceptibility to viral infection the only consequence of these age-related changes in NK cell function? Recently, evidence has emerged that has shown that in addition to eliminating transformed cells, NK cells are involved in many other biological processes such as immune regulation, anti-microbial immune responses and the recognition and elimination of senescent cells, novel functions that involve NK-mediated cytotoxicity and/or cytokine production. Thus, the decrease in NK cell function that accompanies physiological ageing is likely to have wider implications for the health of older adults than originally thought. Here, we give a detailed description of the changes in NK cell biology that accompany human ageing and propose that certain features of the ageing process such as: (i) the increased reactivation rates of latent Mycobacterium tuberculosis, (ii) the slower resolution of inflammatory responses and (iii) the increased incidence of bacterial and fungal infection are attributable in part to an age-associated decline in NK cell function.

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          Most cited references98

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          Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas.

          Although cancer arises from a combination of mutations in oncogenes and tumour suppressor genes, the extent to which tumour suppressor gene loss is required for maintaining established tumours is poorly understood. p53 is an important tumour suppressor that acts to restrict proliferation in response to DNA damage or deregulation of mitogenic oncogenes, by leading to the induction of various cell cycle checkpoints, apoptosis or cellular senescence. Consequently, p53 mutations increase cell proliferation and survival, and in some settings promote genomic instability and resistance to certain chemotherapies. To determine the consequences of reactivating the p53 pathway in tumours, we used RNA interference (RNAi) to conditionally regulate endogenous p53 expression in a mosaic mouse model of liver carcinoma. We show that even brief reactivation of endogenous p53 in p53-deficient tumours can produce complete tumour regressions. The primary response to p53 was not apoptosis, but instead involved the induction of a cellular senescence program that was associated with differentiation and the upregulation of inflammatory cytokines. This program, although producing only cell cycle arrest in vitro, also triggered an innate immune response that targeted the tumour cells in vivo, thereby contributing to tumour clearance. Our study indicates that p53 loss can be required for the maintenance of aggressive carcinomas, and illustrates how the cellular senescence program can act together with the innate immune system to potently limit tumour growth.
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            Activation of NK cells and T cells by NKG2D, a receptor for stress-inducible MICA.

            Stress-inducible MICA, a distant homolog of major histocompatibility complex (MHC) class I, functions as an antigen for gammadelta T cells and is frequently expressed in epithelial tumors. A receptor for MICA was detected on most gammadelta T cells, CD8+ alphabeta T cells, and natural killer (NK) cells and was identified as NKG2D. Effector cells from all these subsets could be stimulated by ligation of NKG2D. Engagement of NKG2D activated cytolytic responses of gammadelta T cells and NK cells against transfectants and epithelial tumor cells expressing MICA. These results define an activating immunoreceptor-MHC ligand interaction that may promote antitumor NK and T cell responses.
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              CD57 defines a functionally distinct population of mature NK cells in the human CD56dimCD16+ NK-cell subset.

              Natural killer (NK) cells are innate immune lymphocytes that express a heterogeneous repertoire of germline-encoded receptors and undergo a distinct pattern of maturation. CD57 is a marker of terminal differentiation on human CD8(+) T cells. Very few newborn or fetal NK cells express CD57; however, the frequency of CD57-bearing NK cells increases with age. We assessed the transcriptional, phenotypic, and functional differences between CD57(+) and CD57(-) NK cells within the CD56(dim) mature NK subset. CD57(+) NK cells express a repertoire of NK-cell receptors, suggestive of a more mature phenotype, and proliferate less when stimulated with target cells and/or cytokines. By contrast, a higher frequency of CD57(+) NK cells produced interferon-γ and demonstrated more potent lytic activity when these cells were stimulated through the activating receptor CD16; however, they are less responsive to stimulation by interleukin-12 and interleukin-18. Finally, CD57 expression is induced on CD57(-)CD56(dim) NK cells after activation by interleukin-2. A combination of a mature phenotype, a higher cytotoxic capacity, a higher sensitivity to stimulation via CD16, with a decreased responsiveness to cytokines, and a decreased capacity to proliferate suggest that CD57(+) NK cells are highly mature and might be terminally differentiated.
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                Author and article information

                Contributors
                Journal
                Ageing Res Rev
                Ageing Res. Rev
                Ageing Research Reviews
                Elsevier Science
                1568-1637
                1872-9649
                1 September 2013
                September 2013
                : 12
                : 4
                : 1069-1078
                Affiliations
                [0005]MRC-ARUK Centre for Musculoskeletal Ageing Research, School of Immunity and Infection, University of Birmingham, Birmingham B15 2TT, UK
                Author notes
                [* ]Corresponding author. Tel.: +44 121 371 3264; fax: +44 121 414 3599. J.Hazeldine@ 123456bham.ac.uk
                Article
                S1568-1637(13)00022-6
                10.1016/j.arr.2013.04.003
                4147963
                23660515
                d0642521-9dbd-48fd-89ca-ae89274057f0
                © 2013 Elsevier B.V. All rights reserved.
                History
                : 6 March 2013
                : 20 April 2013
                : 25 April 2013
                Categories
                Review

                adcc, antibody dependent cell cytotoxicity,apaf-1, apoptosis-activating factor 1,bid, bh3-interacting domain,cad, caspase-activated dnase,cmv, cytomegalovirus,dc, dendritic cell,dln, draining lymph node,fasl, fas ligand,fadd, fas-associated protein with death domain,icad, inhibitor of caspase-activated dnase,ifn-γ, interferon gamma,il-8, interleukin 8,kir, killer cell immunoglobulin like receptor,mhc, major histocompatibility complex,mic, mhc class i-chain-related protein,mip-1α, macrophage inflammatory protein-1-alpha,ncr, natural cytotoxicity receptor,nk cell, natural killer cell,nkcc, natural killer cell cytotoxicity,parp, poly adpribose polymerase,pbls, peripheral blood lymphocytes,pma, phorbol 12-myristate 13-acetate,tb, mycobacterium tuberculosis,tbid, truncated bh3-interacting domain,tnf-α, tumour necrosis factor alpha,th-1, t helper 1 cell,trail, tumor necrosis factor related apoptotic-inducing ligand,natural killer (nk) cells,ageing,immunesenescence

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