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      Adaptive Immune Features of Natural Killer Cells

      research-article
      , ,
      Nature
      Ly49H, DAP12, m157, interferon-gamma, NK1.1

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          Abstract

          In an adaptive immune response, naïve T cells proliferate during infection and generate long-lived memory cells that undergo secondary expansion following re-encounter with the same pathogen. Although Natural Killer cells traditionally have been classified as cells of the innate immune system, they share many similarities with cytotoxic T lymphocytes. In a mouse model of cytomegalovirus (MCMV) infection, we demonstrate that, like T cells, NK cells bearing the virus-specific Ly49H receptor proliferate 100-fold in the spleen and 1000-fold in the liver following infection. Following a contraction phase, Ly49H + NK cells reside in lymphoid and non-lymphoid organs for several months. These self-renewing “memory” NK cells rapidly degranulate and produce cytokines upon reactivation. Adoptive transfer of these NK cells into naïve animals followed by viral challenge results in a robust secondary expansion and protective immunity. These findings reveal novel properties of NK cells previously attributed only to cells of the adaptive immune system.

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          Most cited references37

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          NK cell recognition.

          The integrated processing of signals transduced by activating and inhibitory cell surface receptors regulates NK cell effector functions. Here, I review the structure, function, and ligand specificity of the receptors responsible for NK cell recognition.
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            Effector and memory CTL differentiation.

            Technological advances in recent years have allowed for an ever-expanding ability to analyze and quantify in vivo immune responses. MHC tetramers, intracellular cytokine staining, an increasing repertoire of transgenic and "knockout" mice, and the detailed characterization of a variety of infectious models have all facilitated more precise and definitive analyses of the generation and function of cytotoxic T lymphocytes (CTL). Understanding the mechanisms behind the differentiation of effector and memory CTL is of increasing importance to develop vaccination strategies against a variety of established and emerging infectious diseases. This review focuses on recent advances in our understanding of how effector and memory CTL differentiate and survive in vivo in response to viral or bacterial infection.
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              Effector and memory T-cell differentiation: implications for vaccine development.

              Recent work shows that after stimulation with antigen, CD4+ and CD8+ T cells embark on a programme of proliferation that is closely linked with the acquisition of effector functions and leads ultimately to memory-cell formation. Here, we discuss the signals required for commitment to this programme of development and the factors that might influence its progression. Models of the pathways of effector and memory T-cell differentiation are discussed, and we highlight the implications of this new understanding for the optimization of vaccine strategies.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                0028-0836
                1476-4687
                17 March 2009
                11 January 2009
                29 January 2009
                28 July 2009
                : 457
                : 7229
                : 557-561
                Affiliations
                Department of Microbiology and Immunology and the Cancer Research Institute, University of California, San Francisco, CA 94143
                Author notes
                Reprints and permissions information is available at www.nature.com/reprints. The authors have no conflicting financial interests. Correspondence and requests for materials should be addressed to L.L.L. ( lewis.lanier@ 123456ucsf.edu )
                Article
                nihpa102772
                10.1038/nature07665
                2674434
                19136945
                57f4b5d6-3812-4ee7-a07d-4916ee48859e
                History
                Funding
                Funded by: National Institute of Allergy and Infectious Diseases Extramural Activities : NIAID
                Award ID: R01 AI068129-09 ||AI
                Categories
                Article

                Uncategorized
                nk1.1,ly49h,dap12,interferon-gamma,m157
                Uncategorized
                nk1.1, ly49h, dap12, interferon-gamma, m157

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