59
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Natural Killer Cells: Development, Maturation, and Clinical Utilization

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Natural killer (NK) cells are the predominant innate lymphocyte subsets that mediate anti-tumor and anti-viral responses, and therefore possess promising clinical utilization. NK cells do not express polymorphic clonotypic receptors and utilize inhibitory receptors (killer immunoglobulin-like receptor and Ly49) to develop, mature, and recognize “ self” from “ non-self.” The essential roles of common gamma cytokines such as interleukin (IL)-2, IL-7, and IL-15 in the commitment and development of NK cells are well established. However, the critical functions of pro-inflammatory cytokines IL-12, IL-18, IL-27, and IL-35 in the transcriptional-priming of NK cells are only starting to emerge. Recent studies have highlighted multiple shared characteristics between NK cells the adaptive immune lymphocytes. NK cells utilize unique signaling pathways that offer exclusive ways to genetically manipulate to improve their effector functions. Here, we summarize the recent advances made in the understanding of how NK cells develop, mature, and their potential translational use in the clinic.

          Related collections

          Most cited references370

          • Record: found
          • Abstract: found
          • Article: not found

          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.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Up on the tightrope: natural killer cell activation and inhibition.

            Natural killer (NK) cells circulate through the blood, lymphatics and tissues, on patrol for the presence of transformed or pathogen-infected cells. As almost all NK cell receptors bind to host-encoded ligands, signals are constantly being transmitted into NK cells, whether they interact with normal or abnormal cells. The sophisticated repertoire of activating and inhibitory receptors that has evolved to regulate NK cell activity ensures that NK cells protect hosts against pathogens, yet prevents deleterious NK cell-driven autoimmune responses. Here I highlight recent advances in our understanding of the structural properties and signaling pathways of the inhibitory and activating NK cell receptors, with a particular focus on the ITAM-dependent activating receptors, the NKG2D-DAP10 receptor complexes and the CD244 receptor system.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              In search of the ‘missing self’: MHC molecules and NK cell recognition

              Immunology Today, 11, 237-244
                Bookmark

                Author and article information

                Contributors
                URI : https://frontiersin.org/people/u/577602
                URI : https://frontiersin.org/people/u/255068
                URI : https://frontiersin.org/people/u/30467
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                13 August 2018
                2018
                : 9
                : 1869
                Affiliations
                [1] 1Laboratory of Molecular Immunology and Immunotherapy, Blood Research Institute, Blood Center of Wisconsin , Milwaukee, WI, United States
                [2] 2Department of Microbiology and Immunology, Medical College of Wisconsin , Milwaukee, WI, United States
                [3] 3Department of Pediatrics, Medical College of Wisconsin , Milwaukee, WI, United States
                [4] 4Department of Medicine, Medical College of Wisconsin , Milwaukee, WI, United States
                [5] 5Center of Excellence in Prostate Cancer, Medical College of Wisconsin , Milwaukee, WI, United States
                Author notes

                Edited by: Laurent Brossay, Brown University, United States

                Reviewed by: Michael G. Brown, University of Virginia, United States; Stephen Noel Waggoner, Cincinnati Children’s Hospital Medical Center, United States

                *Correspondence: Subramaniam Malarkannan, subra.malar@ 123456bcw.edu

                Specialty section: This article was submitted to NK and Innate Lymphoid Cell Biology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2018.01869
                6099181
                30150991
                6692336b-a7b0-471c-b6cf-715de1b5d153
                Copyright © 2018 Abel, Yang, Thakar and Malarkannan.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 May 2018
                : 30 July 2018
                Page count
                Figures: 9, Tables: 0, Equations: 0, References: 340, Pages: 23, Words: 19920
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: R01 AI102893
                Funded by: National Cancer Institute 10.13039/100000054
                Award ID: R01 CA179363
                Categories
                Immunology
                Review

                Immunology
                developmental stages,human,mouse,natural killer cells,effector functions
                Immunology
                developmental stages, human, mouse, natural killer cells, effector functions

                Comments

                Comment on this article