Commensal gut bacteria: mechanisms of immune modulation

被引:280
作者
Kelly, D [1 ]
Conway, S [1 ]
Aminov, R [1 ]
机构
[1] Rowett Res Inst, Gut Immunol Grp, Aberdeen AB21 9SB, Scotland
关键词
D O I
10.1016/j.it.2005.04.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucosal immune responses to pathogenic gut bacteria and the mechanisms that govern disease progression and outcome have been researched intensely for decades. More recently, the influence of the resident non-pathogenic or 'commensal' microflora on mucosal immune function and gut health has emerged as an area of scientific and clinical importance. Major differences occur in the mucosal immune response to pathogens and commensals. In part, this functional dichotomy is explained by the presence of virulence factors in pathogenic species, which are generally absent in commensals. Additionally, immunological 'unresponsiveness' towards the resident commensal microflora is thought to permit their successful colonisation and co-existence within the host gut. However, evidence of an active dialogue between members of the commensal microflora and the host mucosal immune system is rapidly unfolding. This crosstalk is likely to affect immunological tolerance and homeostasis within the gut and to explain some of the differential host responses to commensal and pathogenic bacteria.
引用
收藏
页码:326 / 333
页数:8
相关论文
共 88 条
[1]   TLR4 and MD-2 expression is regulated by immune-mediated signals in human intestinal epithelial cells [J].
Abreu, MT ;
Arnold, ET ;
Thomas, LS ;
Gonsky, R ;
Zhou, YH ;
Hu, B ;
Arditi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20431-20437
[2]   Colitogenic Th1 cells are present in the antigen-experienced T cell pool in normal mice:: Control by CD4+ regulatory T cells and IL-10 [J].
Asseman, C ;
Read, S ;
Powrie, F .
JOURNAL OF IMMUNOLOGY, 2003, 171 (02) :971-978
[3]   Secretion of microbicidal α-defensins by intestinal Paneth cells in response to bacteria [J].
Ayabe, T ;
Satchell, DP ;
Wilson, CL ;
Parks, WC ;
Selsted, ME ;
Ouellette, AJ .
NATURE IMMUNOLOGY, 2000, 1 (02) :113-118
[4]   The gut microbiota as an environmental factor that regulates fat storage [J].
Bäckhed, F ;
Ding, H ;
Wang, T ;
Hooper, LV ;
Koh, GY ;
Nagy, A ;
Semenkovich, CF ;
Gordon, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (44) :15718-15723
[5]   In vitro and ex vivo activation of the TLR5 signaling pathway in intestinal epithelial cells by a commensal Escherichia coli strain [J].
Bambou, JC ;
Giraud, A ;
Menard, S ;
Begue, B ;
Rakotobe, S ;
Heyman, M ;
Taddei, FO ;
Cerf-Bensussan, N ;
Gaboriau-Routhiau, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (41) :42984-42992
[6]   Carcinoembryonic antigen (CEA) and CEA-related cell adhesion molecule 1 (CEACAM1), apically expressed on human colonic M cells, are potential receptors for microbial adhesion [J].
Baranov, V ;
Hammarström, S .
HISTOCHEMISTRY AND CELL BIOLOGY, 2004, 121 (02) :83-89
[7]   Toll-like receptor 4 signaling by intestinal microbes influences susceptibility to food allergy [J].
Bashir, MEH ;
Louie, S ;
Shi, HN ;
Nagler-Anderson, C .
JOURNAL OF IMMUNOLOGY, 2004, 172 (11) :6978-6987
[8]   Constitutive p40 promoter activation and IL-23 production in the terminal ileum mediated by dendritic cells [J].
Becker, C ;
Wirtz, S ;
Blessing, M ;
Pirhonen, J ;
Strand, D ;
Bechthold, O ;
Frick, J ;
Galle, PR ;
Autenrieth, I ;
Neurath, MF .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (05) :693-706
[9]  
Bollinger RR, 2003, IMMUNOLOGY, V109, P580
[10]   The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses [J].
Boone, DL ;
Turer, EE ;
Lee, EG ;
Ahmad, RC ;
Wheeler, MT ;
Tsui, C ;
Hurley, P ;
Chien, M ;
Chai, S ;
Hitotsumatsu, O ;
McNally, E ;
Pickart, C ;
Ma, A .
NATURE IMMUNOLOGY, 2004, 5 (10) :1052-1060