MHC class I alleles and their exploration of the antigen-processing machinery

被引:47
作者
Groothuis, TAM [1 ]
Griekspoor, AC [1 ]
Neijssen, JJ [1 ]
Herberts, CA [1 ]
Neefjes, JJ [1 ]
机构
[1] Netherlands Canc Inst, Div Tumour Biol, NL-1066 CX Amsterdam, Netherlands
关键词
D O I
10.1111/j.0105-2896.2005.00305.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
At the cell surface, major histocompatibility complex (MHC) class I molecules present fragments of intracellular antigens to the immune system. This is the end result of a cascade of events initiated by multiple steps of proteolysis. Only a small part of the fragments escapes degradation by interacting with the peptide transporter associated with antigen presentation and is translocated into the endoplasmic reticulum lumen for binding to MHC class I molecules. Subsequently, these newly formed complexes can be transported to the plasma membrane for presentation. Every step in this process confers specificity and determines the ultimate result: presentation of only few fragments from a given antigen. Here, we introduce the players in the antigen processing and presentation cascade and describe their specificity and allelic variation. We highlight MHC class I alleles, which are not only different in sequence but also use different aspects of the antigen presentation pathway to their advantage: peptide acquaintance.
引用
收藏
页码:60 / 76
页数:17
相关论文
共 160 条
[1]   Access of soluble antigens to the endoplasmic reticulum can explain cross-presentation by dendritic cells [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
NATURE IMMUNOLOGY, 2005, 6 (01) :107-113
[2]   Cellular mechanisms governing cross-presentation of exogenous antigens [J].
Ackerman, AL ;
Cresswell, P .
NATURE IMMUNOLOGY, 2004, 5 (07) :678-684
[3]  
ACKRILL AM, 1988, ONCOGENE, V3, P483
[4]   EXPRESSION OF HAMSTER MHC CLASS-I ANTIGENS IN TRANSFORMED-CELLS AND TUMORS INDUCED BY HUMAN ADENOVIRUSES [J].
ACKRILL, AM ;
BLAIR, GE .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (11) :1745-1750
[5]   The ER-luminal domain of the HCMV glycoprotein US6 inhibits peptide translocation by TAP [J].
Ahn, K ;
Gruhler, A ;
Galocha, B ;
Jones, TR ;
Wiertz, EJHJ ;
Ploegh, HL ;
Peterson, PA ;
Yang, Y ;
Fruh, K .
IMMUNITY, 1997, 6 (05) :613-621
[6]   Molecular mechanism and species specificity of TAP inhibition by herpes simplex virus protein ICP47 [J].
Ahn, K ;
Meyer, TH ;
Uebel, S ;
Sempe, P ;
Djaballah, H ;
Yang, Y ;
Peterson, PA ;
Fruh, K ;
Tampe, R .
EMBO JOURNAL, 1996, 15 (13) :3247-3255
[7]   Mechanism and function of deubiquitinating enzymes [J].
Amerik, AY ;
Hochstrasser, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1695 (1-3) :189-207
[8]  
Andersen MH, 1999, J IMMUNOL, V163, P3812
[9]   IMPAIRED INTRACELLULAR-TRANSPORT OF CLASS-I MHC ANTIGENS AS A POSSIBLE MEANS FOR ADENOVIRUSES TO EVADE IMMUNE SURVEILLANCE [J].
ANDERSSON, M ;
PAABO, S ;
NILSSON, T ;
PETERSON, PA .
CELL, 1985, 43 (01) :215-222
[10]  
Apostolopoulos Vasso, 2004, Expert Rev Vaccines, V3, P151, DOI 10.1586/14760584.3.2.151