Mucosal immune responses

被引:77
作者
Acheson, DWK [1 ]
Luccioli, S [1 ]
机构
[1] US FDA, CFSAN, DHSS, College Pk, MD 20740 USA
关键词
mucosal immunity; intestinal epithelial cells; food-borne pathogens; gut-associated lymphoid tissue; follicle associated epithelia;
D O I
10.1016/j.bpg.2003.11.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The host gastrointestinal tract is exposed to countless numbers of foreign antigens and has embedded a unique and complex network of immunological and non-immunological mechanisms, often termed the gastrointestinal 'mucosal barrier', to protect the host from potentially harmful pathogens while at the same time 'tolerating' other resident microbes to allow absorption and utilization of nutrients. Of the many important roles of this barrier, it is the distinct responsibility of the mucosal immune system to sample and discriminate between harmful and beneficial antigens and to prevent entry of food-borne pathogens through the gastrointestinal (GI) tract. This system comprises an immunological network termed the gut-associated lymphoid tissue (GALT) that consists of unique arrangements of B cells, T cells and phagocytes which sample luminal antigens through specialized epithelia termed the follicle associated epithelia (FAE) and orchestrate co-ordinated molecular responses between immune cells and other components of the mucosal barrier. Certain pathogens have developed ways to bypass and/or withstand defence by the mucosal immune system to establish disease in the host. Some 'opportunistic' pathogens (such as Clostridium difficile) take advantage of host or other factors (diet, stress, antibiotic use) which may alter or weaken the response of the immune system. Other pathogens have developed mechanisms for invading gastrointestinal epithelium and evading phagocytosis/destruction by immune system defences. Once cellular invasion occurs, host responses are activated to limit local mucosal damage and repel the foreign influence. Some pathogens (Shigella spp, parasites and viruses) primarily establish localized disease while others (Salmonella, Yersinia, Listeria) use the lymphatic system to enter organs or the bloodstream and cause more systemic illness. In some cases, pathogens (Helicobacter pylori and Salmonella typhi) colonize the GI tract or associated lymphoid structures for extended periods of time and these persistent pathogens may also be potential triggers for other chronic or inflammatory diseases, including inflammatory bowel disease and malignancies. The ability of certain pathogens to avoid or withstand the host's immune assault and/or utilize these host responses to their own advantage (i.e. enhance further colonization) will dictate the pathogen's success in promoting illness and furthering its own survival.
引用
收藏
页码:387 / 404
页数:18
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共 90 条
  • [21] A novel member of the transforming growth factor-β (TGF-β) superfamily from the filarial nematodes Brugia malayi and B-pahangi
    Gomez-Escobar, N
    Lewis, E
    Maizels, RM
    [J]. EXPERIMENTAL PARASITOLOGY, 1998, 88 (03) : 200 - 209
  • [22] Intestinal bacterial overgrowth and bacterial translocation in cirrhotic rats with ascites
    Guarner, C
    Runyon, BA
    Young, S
    Heck, M
    Sheikh, MY
    [J]. JOURNAL OF HEPATOLOGY, 1997, 26 (06) : 1372 - 1378
  • [23] Genetic and functional analysis of a PmrA-PmrB-regulated locus necessary for lipopolysaccharide modification, antimicrobial peptide resistance, and oral virulence of Salmonella enterica serovar typhimurium
    Gunn, JS
    Ryan, SS
    Van Velkinburgh, JC
    Ernst, RK
    Miller, SI
    [J]. INFECTION AND IMMUNITY, 2000, 68 (11) : 6139 - 6146
  • [24] Regulation of lipid a modifications by Salmonella typhimurium virulence genes phoP-phoQ
    Guo, L
    Lim, KB
    Gunn, JS
    Bainbridge, B
    Darveau, RP
    Hackett, M
    Miller, SI
    [J]. SCIENCE, 1997, 276 (5310) : 250 - 253
  • [25] Virulence functions of autotransporter proteins
    Henderson, IR
    Nataro, JP
    [J]. INFECTION AND IMMUNITY, 2001, 69 (03) : 1231 - 1243
  • [26] The Salmonella invasin SipB induces macrophage apoptosis by binding to caspase-1
    Hersh, D
    Monack, DM
    Smith, MR
    Ghori, N
    Falkow, S
    Zychlinsky, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) : 2396 - 2401
  • [27] Bacterial strategies for overcoming host innate and adaptive immune responses
    Hornef, MW
    Wick, MJ
    Rhen, M
    Normark, S
    [J]. NATURE IMMUNOLOGY, 2002, 3 (11) : 1033 - 1040
  • [28] Shiga toxin translocation across intestinal epithelial cells is enhanced by neutrophil transmigration
    Hurley, BP
    Thorpe, CM
    Acheson, DWK
    [J]. INFECTION AND IMMUNITY, 2001, 69 (10) : 6148 - 6155
  • [29] Host microbe interactions: bacteria - Innate immune response: attack and counter-attack - Editorial overview
    Isberg, RR
    Normark, S
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (01) : 13 - 15
  • [30] Downregulation of bactericidal peptides in enteric infections: A novel immune escape mechanism with bacterial DNA as a potential regulator
    Islam, D
    Bandholtz, L
    Nilsson, J
    Wigzell, H
    Christensson, B
    Agerberth, B
    Gudmundsson, GH
    [J]. NATURE MEDICINE, 2001, 7 (02) : 180 - 185