Mucosa-associated lymphoid tissues in the aerodigestive tract: Their shared and divergent traits and their importance to the orchestration of the mucosal immune system

被引:49
作者
Kunisawa, J [1 ]
Fukuyama, S [1 ]
Kiyono, H [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Microbiol & Immunol, Div Mucosal Immunol,CREST,JST,Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.2174/1566524054863924
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
As inductive tissues for the initiation of antigen-specific T and B cell responses, the various mucosa-associated lymphoid tissues (MALT) of the aerodigestive tract, which include gut-associated lymphoid tissue (GALT), nasopharynx-associated lymphoid tissue (NALT) and bronchus-associated lymphoid tissue (BALT), share many histological and immunological characteristics. However, recent advances in our molecular and cellular understanding of immunological development have revealed that the various types of MALT also exhibit different molecular and cellular interactions for their organogenesis. In this review, we delineate the distinctive features of GALT, NALT and BALT and seek to show the role played by those features in the regulation of mucosal tissue organogenesis, the mucosal immune system, and mucosal homeostasis, all in an attempt to provide insights which might lead to a prospective mucosal vaccine.
引用
收藏
页码:557 / 572
页数:16
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共 169 条
  • [41] Ulex europaeus 1 lectin targets microspheres to mouse Peyer's patch M-cells in vivo
    Foster, N
    Clark, MA
    Jepson, MA
    Hirst, BH
    [J]. VACCINE, 1998, 16 (05) : 536 - 541
  • [42] Interleukin 2 (IL-2) and interleukin 7 (IL-7) reciprocally induce IL-7 and IL-2 receptors on gamma delta T-cell receptor-positive intraepithelial lymphocytes
    Fujihashi, K
    Kawabata, S
    Hiroi, T
    Yamamoto, M
    McGhee, JR
    Nishikawa, SI
    Kiyono, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) : 3613 - 3618
  • [43] Fujiura Y, 1996, J IMMUNOL, V156, P2710
  • [44] Initiation of NALT organogenesis is independent of the IL-7R, LTβR, and NIK signaling pathways but requires the Id2 gene and CD3-CD4+CD45+ cells
    Fukuyama, S
    Hiroi, T
    Yokota, Y
    Rennert, PD
    Yanagita, M
    Kinoshita, N
    Terawaki, S
    Shikina, T
    Yamamoto, M
    Kurono, Y
    Kiyono, H
    [J]. IMMUNITY, 2002, 17 (01) : 31 - 40
  • [45] The lymphotoxin β receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues
    Fütterer, A
    Mink, K
    Luz, A
    Kosco-Vilbois, MH
    Pfeffer, K
    [J]. IMMUNITY, 1998, 9 (01) : 59 - 70
  • [46] REGIONAL DIFFERENCES IN GLYCOCONJUGATES OF INTESTINAL M-CELLS IN MICE - POTENTIAL TARGETS FOR MUCOSAL VACCINES
    GIANNASCA, PJ
    GIANNASCA, KT
    FALK, P
    GORDON, JI
    NEUTRA, MR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1994, 267 (06): : G1108 - G1121
  • [47] Costimulation of CD8αβ T cells by NKG2D via engagement by MIC induced on virus-infected cells
    Groh, V
    Rhinehart, R
    Randolph-Habecker, J
    Topp, MS
    Riddell, SR
    Spies, T
    [J]. NATURE IMMUNOLOGY, 2001, 2 (03) : 255 - 260
  • [48] Recombinant Norwalk virus-like particles administered intranasally to mice induce systemic and mucosal (fecal and vaginal) immune responses
    Guerrero, RA
    Ball, JM
    Krater, SS
    Pacheco, SE
    Clements, JD
    Estes, MK
    [J]. JOURNAL OF VIROLOGY, 2001, 75 (20) : 9713 - 9722
  • [49] Extrathymic T cell lymphopoiesis: Ontogeny and contribution to gut intraepithelial lymphocytes in athymic and euthymic mice
    Guy-Grand, D
    Azogui, O
    Celli, S
    Darche, S
    Nussenzweig, MC
    Kourilsky, P
    Vassalli, P
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (03) : 333 - 341
  • [50] 2 GUT INTRAEPITHELIAL CD8+ LYMPHOCYTE POPULATIONS WITH DIFFERENT T-CELL RECEPTORS - A ROLE FOR THE GUT EPITHELIUM IN T-CELL DIFFERENTIATION
    GUYGRAND, D
    CERFBENSUSSAN, N
    MALISSEN, B
    MALASSISSERIS, M
    BRIOTTET, C
    VASSALLI, P
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (02) : 471 - 481