Innate and adaptive lymphoid cells in the human liver

被引:286
作者
Doherty, DG [1 ]
O'Farrelly, C [1 ]
机构
[1] St Vincents Univ Hosp, Educ & Res Ctr, Dublin 4, Ireland
关键词
D O I
10.1034/j.1600-0528.2002.017416.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Because of its location and function, the liver is continuously exposed to a large antigenic load that includes pathogens, toxins, tumor cells and harmless dietary antigens. The range of local immune mechanisms required to cope with this diverse immunological challenge is now being appreciated. The liver has an "epithelial constitution" and contains large numbers of phagocytic cells, antigen-presenting cells and lymphocytes and is a site for the production of cytokines, complement components and acute phase proteins. In this review, we focus on the hepatic lymphoid system, which is currently emerging as an important arm of the immune system in the liver for targeting pathogens as well as for the recognition of cells that are modified as a result of infection or tumor transformation. We show that this organ contains a heterogeneity of lymphoid cells with diverse recognition mechanisms and functions. There are conventional T lymphocytes that use clonotypic receptors to identify and respond to antigenic peptides presented in the context of polymorphic class I and class II major histocompatibilty complex (MHC) molecules. But these cells are outnumbered by lymphoid cells that recognize common structures using receptors with limited diversity. These mediators of innate immunity against infectious pathogens and malignant cells respond immediately to stimuli and function as a temporal land perhaps evolutionary) bridge for the adaptive immune response.
引用
收藏
页码:5 / 20
页数:16
相关论文
共 108 条
  • [1] Physiological responses of extrathymic T cells in the liver
    Abo, T
    Kawamura, T
    Watanabe, H
    [J]. IMMUNOLOGICAL REVIEWS, 2000, 174 : 135 - 149
  • [2] Abo T, 1994, Int Rev Immunol, V11, P61, DOI 10.3109/08830189409061717
  • [3] Interferon gamma production by natural killer (NK) cells and NK1.1(+) T cells upon NKR-P1 cross-linking
    Arase, H
    Arase, N
    Saito, T
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) : 2391 - 2396
  • [4] BALLAS ZK, 1990, J IMMUNOL, V145, P1039
  • [5] THE ROLE OF NATURAL-KILLER-CELLS IN INNATE RESISTANCE TO INFECTION
    BANCROFT, GJ
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1993, 5 (04) : 503 - 510
  • [6] BARNABA V, 1994, J IMMUNOL, V152, P3074
  • [7] Battistini L, 1997, J IMMUNOL, V159, P3723
  • [8] Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA
    Bauer, Stefan
    Groh, Veronika
    Wu, Jun
    Steinle, Alexander
    Phillips, Joseph H.
    Lanier, Lewis L.
    Spies, Thomas
    [J]. JOURNAL OF IMMUNOLOGY, 2018, 200 (07) : 2231 - 2233
  • [9] RECOGNITION OF A LIPID ANTIGEN BY CD1-RESTRICTED ALPHA-BETA(+) T-CELLS
    BEEKMAN, EM
    PORCELLI, SA
    MORITA, CT
    BEHAR, SM
    FURLONG, ST
    BRENNER, MB
    [J]. NATURE, 1994, 372 (6507) : 691 - 694
  • [10] CD1 RECOGNITION BY MOUSE NK1(+) T-LYMPHOCYTES
    BENDELAC, A
    LANTZ, O
    QUIMBY, ME
    YEWDELL, JW
    BENNINK, JR
    BRUTKIEWICZ, RR
    [J]. SCIENCE, 1995, 268 (5212) : 863 - 865