Regulation of antigen presentation and cross-presentation in the dendritic cell network: Facts, hypothesis, and immunological implications

被引:126
作者
Wilson, NS [1 ]
Villadangos, JA
机构
[1] Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3050, Australia
[2] Walter & Eliza Hall Inst Med Res, Cooperat Res Ctr Vaccine Technol, Parkville, Vic 3050, Australia
来源
ADVANCES IN IMMUNOLOGY, VOL 86 | 2005年 / 86卷
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0065-2776(04)86007-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are central to the maintenance of immunological tolerance and the initiation and control of immunity. The antigen-presenting properties of DCs enable them to present a sample of self and foreign proteins, contained within an organism at any given time, to the T-cell repertoire. DCs achieve this communication with T cells by displaying antigenic peptides bound to MHC I and MHC II molecules. Here we review the studies carried out over the past 15 years to characterize these antigen presentation mechanism, emphasizing their significance in relation to DC function in vivo. The life cycles of different DC populations found in vivo are described. Furthermore, we provide a critical assessment Of the studies that examine the mechanisms controlling DC MHC class II antigen presentation, which have often reached contradictory conclusions. Finally, we review findings pertaining to the biological mechanisms that enable DCs to present exogenous antigens on their MHC class I molecules, a process known as cross-presentation. Throughout, we highlight what we consider to be major knowledge gaps in the field and speculate on possible directions for future research.
引用
收藏
页码:241 / 305
页数:65
相关论文
共 298 条
[181]   Constitutive macropinocytosis allows TAP-dependent major histocompatibility complex class I presentation of exogenous soluble antigen by bone marrow-derived dendritic cells [J].
Norbury, CC ;
Chambers, BJ ;
Prescott, AR ;
Ljunggren, HG ;
Watts, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (01) :280-288
[182]   The cytoplasmic tail of invariant chain regulates endosome fusion and morphology [J].
Nordeng, TW ;
Gregers, TF ;
Kongsvik, TL ;
Méresse, S ;
Gorvel, JP ;
Jourdan, F ;
Motta, A ;
Bakke, O .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (06) :1846-1856
[183]   Mouse plasmacytoid cells:: Long-lived cells, heterogeneous in surface phenotype and function, that differentiate into CD8+ dendritic cells only after microbial stimulus [J].
O'Keeffe, M ;
Hochrein, H ;
Vremec, D ;
Caminschi, I ;
Miller, JL ;
Anders, EM ;
Wu, L ;
Lahoud, H ;
Henri, S ;
Scott, B ;
Hertzog, P ;
Tatarczuch, L ;
Shortman, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (10) :1307-1319
[184]   Dendritic cell precursor populations of mouse blood:: identification of the murine homologues of human blood plasmacytoid pre-DC2 and CD11c+ DC1 precursors [J].
O'Keeffe, M ;
Hochrein, H ;
Vremec, D ;
Scott, B ;
Hertzog, P ;
Tatarczuch, L ;
Shortman, K .
BLOOD, 2003, 101 (04) :1453-1459
[185]   Effects of administration of progenipoietin 1, Flt-3 ligand, granulocyte colony-stimulating factor, and pegylated granulocyte-macrophage colony-stimulating factor on dendritic cell subsets in mice [J].
O'Keeffe, M ;
Hochrein, H ;
Vremec, D ;
Pooley, J ;
Evans, R ;
Woulfe, S ;
Shortman, K .
BLOOD, 2002, 99 (06) :2122-2130
[186]   Dendritic cells from malaria-infected mice are fully functional APC [J].
Perry, JA ;
Rush, A ;
Wilson, RJ ;
Olver, CS ;
Avery, AC .
JOURNAL OF IMMUNOLOGY, 2004, 172 (01) :475-482
[187]   SEGREGATION OF MHC CLASS-II MOLECULES FROM MHC CLASS-I MOLECULES IN THE GOLGI-COMPLEX FOR TRANSPORT TO LYSOSOMAL COMPARTMENTS [J].
PETERS, PJ ;
NEEFJES, JJ ;
OORSCHOT, V ;
PLOEGH, HL ;
GEUZE, HJ .
NATURE, 1991, 349 (6311) :669-676
[188]   Developmental regulation of invariant chain proteolysis controls MHC class II trafficking in mouse dendritic cells [J].
Pierre, P ;
Mellman, I .
CELL, 1998, 93 (07) :1135-1145
[189]   Developmental regulation of MHC class II transport in mouse dendritic cells [J].
Pierre, P ;
Turley, SJ ;
Gatti, E ;
Hull, M ;
Meltzer, J ;
Mirza, A ;
Inaba, K ;
Steinman, RM ;
Mellman, I .
NATURE, 1997, 388 (6644) :787-792
[190]  
PIETERS J, 1993, J CELL SCI, V106, P831