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The mucosal immune system for vaccine development
Authors:Aayam Lamichhane  Tatsuhiko Azegami  Hiroshi Kiyono
Institution:1. Division of Mucosal Immunology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan;2. International Research and Development Center for Mucosal Vaccines, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan;3. Department of Internal Medicine, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan
Abstract:Mucosal surfaces are continuously exposed to the external environment and therefore represent the largest lymphoid organ of the body. In the mucosal immune system, gut-associated lymphoid tissues (GALTs), including Peyer's patches and isolated lymphoid follicles, play an important role in the induction of antigen-specific immune responses in the gut. GALTs have unique organogenesis characteristics and interact with the network of dendritic cells and T cells for the simultaneous induction and regulation of IgA responses and oral tolerance. In these lymphoid tissues, antigens are up taken by M cells in the epithelial layer, and antigen-specific immune responses are subsequently initiated by GALT cells. Nasopharynx- and tear-duct-associated lymphoid tissues (NALTs and TALTs) are key organized lymphoid structures in the respiratory tract and ocular cavities, respectively, and have been shown to interact with each other. Mucosal surfaces are also characterized by host-microbe interactions that affect the genesis and maturation of mucosa-associated lymphoid tissues and the induction and regulation of innate and acquired mucosal immune responses. Because most harmful pathogens enter the body through mucosal surfaces by ingestion, inhalation, or sexual contact, the mucosa is a candidate site for vaccination. Mucosal vaccination has some physiological and practical advantages, such as decreased costs and reduced risk of needle-stick injuries and transmission of bloodborne diseases, and it is painless. Recently, the application of modern bioengineering and biochemical engineering technologies, including gene transformation and manipulation systems, resulted in the development of systems to express vaccine antigens in transgenic plants and nanogels, which will usher in a new era of delivery systems for mucosal vaccine antigens. In this review, based on some of our research group's thirty seven years of progress and effort, we highlight the unique features of mucosal immune systems and the application of mucosal immunity to the development of a new generation of vaccines.
Keywords:APC  antigen presenting cell  cCHP  cationic type of cholesteryl group-bearing pullulan  CCL  CC chemokine ligand  CCR  CC chemokine receptor  CMIS  common mucosal immune system  CT  cholera toxin  CTB  cholera enterotoxin B subunit  CXCL  CXC chemokine ligand  CXCR  CXC chemokine receptor  DC  dendritic cell  Ig  immunoglobulin  IgA+ B cell  IgA-committed B cell  FAE  follicle-associated epithelium  GALT  gut-associated lymphoid tissue  GI  gastrointestinal  gp2  glycoprotein 2  Id2  inhibitor of DNA binding 2  IL  Interleukin  ILF  isolated lymphoid follicle  LP  lamina propria  LPS  lipopolysaccharide  LT  heat-labile enterotoxin  LTB  heat-labile enterotoxin B subunit  MALT  mucosa-associated lymphoid tissue  M cell  microfold/membranous cell  NALT  nasopharynx-associated lymphoid tissue  PP  Peyer's patch  PspA  pneumococcal surface protein A  RANKL  receptor activator of nuclear factor κB ligand  RORγt  retinoic-acid-receptor-related orphan receptor-γ  SIgA  secretory immunoglobulin A  TALT  tear duct-associated lymphoid tissue  TGF  transforming growth factor  Th  T helper  TLR  toll-like receptor  TNFR  tumor necrosis factor receptor  Treg  regulatory T  UEA-1  ulex europaeus agglutinin 1
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