Ins and outs of dendritic cells

被引:80
作者
Schuurhuis, DH [1 ]
Fu, N [1 ]
Ossendorp, F [1 ]
Melief, CJM [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, Leiden, Netherlands
关键词
dendritic cell; antigen presentation; Th1/Th2; cell; cytotoxic T lymphocytes; tumor; migration; maturation; CD40/CD40L; Fc receptor;
D O I
10.1159/000092002
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DC) are professional antigen-presenting eel Is which are strategically positioned at the boundaries between the inner and the outside world, in this way bridging innate and adaptive immunity. DC can initiate T cell responses against microbial pathogens and tumors due to their capacity to stimulate naive T cells. The development of DC occurs in distinct stages. DC precursors develop in the bone marrow and home to a large variety of tissues. Immature DC capture antigen (Ag) and, following proinflammatory signals, migrate to the lymphoid organs where, after maturation, they present captured Ag to naive T cells, thereby inducing differentiation of naive T cells into effector T cells. An important cognate event in the development of cell-mediated immunity is the interaction between CD40 and CD40 ligand. Ligation of CD40 on DC by its ligand results in maturation of the DC. In addition to CD40 ligand (expressed by activated Th cells), inflammatory cytokines, bacterial components or Ag-Ab immune complexes can induce maturation of DC. Maturation of DC is crucial for the priming of efficient T cell responses and is characterized by a decreased Ag processing capacity, an increased cell surface expression of MHC and costimulatory molecules, and rearrangement of cytoskeleton,adhesion molecules, and cytokine receptors. Mature DC migrate from peripheral tissues to secondary lymphoid organs, where T cell priming occurs. DC are not only critical in initiating T cell immunity, they also play a role in the induction of T cell tolerance and the regulation of the type of T cell response that is induced. Here we give an overview of the dendritic cell system. Copyright (C) 2006 S. Karger AG, Basel.
引用
收藏
页码:53 / 72
页数:20
相关论文
共 266 条
[1]   Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12889-12894
[2]   A dendritic-cell-derived C-C chemokine that preferentially attracts naive T cells [J].
Adema, GJ ;
Hartgers, F ;
Verstraten, R ;
deVries, E ;
Marland, G ;
Menon, S ;
Foster, J ;
Xu, YM ;
Nooyen, P ;
McClanahan, T ;
Bacon, KB ;
Figdor, CG .
NATURE, 1997, 387 (6634) :713-717
[3]   Cutting edge: Cell surface expression and lipopolysaccharide signaling via the Toll-like receptor 4-MD-2 complex on mouse peritoneal macrophages [J].
Akashi, S ;
Shimazu, R ;
Ogata, H ;
Nagai, Y ;
Takeda, K ;
Kimoto, M ;
Miyake, K .
JOURNAL OF IMMUNOLOGY, 2000, 164 (07) :3471-3475
[4]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[5]   Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes [J].
Albert, ML ;
Pearce, SFA ;
Francisco, LM ;
Sauter, B ;
Roy, P ;
Silverstein, RL ;
Bhardwaj, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) :1359-1368
[6]   Fc receptor signaling and trafficking: a connection for antigen processing [J].
Amigorena, S ;
Bonnerot, C .
IMMUNOLOGICAL REVIEWS, 1999, 172 :279-284
[7]   Fc receptors for IgG and antigen presentation on MHC class I and class II molecules [J].
Amigorena, S ;
Bonnerot, C .
SEMINARS IN IMMUNOLOGY, 1999, 11 (06) :385-390
[8]   Up-regulation of TLR9 gene expression by LPS in mouse macrophages via activation of NF-κB, ERK and p38 MAPK signal pathways [J].
An, HZ ;
Xu, HM ;
Yu, YZ ;
Zhang, MH ;
Qi, RZ ;
Yan, XY ;
Liu, SX ;
Wang, WY ;
Guo, ZH ;
Qin, ZH ;
Cao, XT .
IMMUNOLOGY LETTERS, 2002, 81 (03) :165-169
[9]  
Andre F, 2001, ADV EXP MED BIOL, V495, P349
[10]  
ANGELISOVA P, 1994, IMMUNOGENETICS, V39, P249