Accessory molecules in the assembly of major histocompatibility complex class I/peptide complexes:: how essential are they for CD8+ T-cell immune responses?

被引:29
作者
Garbi, N
Tanaka, S
van den Broek, M
Momburg, F
Hämmerling, GJ
机构
[1] German Canc Res Ctr, Div Mol Immunol, D-69120 Heidelberg, Germany
[2] Sapporo City Gen Hosp, Dept Pathol, Sapporo, Hokkaido, Japan
[3] Inst Expt Immunol, Zurich, Switzerland
关键词
D O I
10.1111/j.0105-2896.2005.00303.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
Assembly of major histocompatibility complex (MHC) class I molecules in the endoplasmic reticulum is a highly coordinated process that results in abundant class I/peptide complexes at the cell surface for recognition by CD8(+) T cells and natural killer cells. During the assembly process, a number of chaperones and accessory molecules, such as transporter associated with antigen processing, tapasin, ER60, and calreticulin, assist newly synthesized class I molecules to facilitate loading of antigenic peptides and to optimize the repertoire of surface class I/peptide complexes. This review focuses on the relative importance of these accessory molecules for CD8(+) T-cell responses in vivo and discusses reasons that may help explain why some CD8(+) T-cell responses develop normally in mice deficient in components of class I assembly, despite impaired antigen presentation.
引用
收藏
页码:77 / 88
页数:12
相关论文
共 94 条
[1]   Cellular mechanisms governing cross-presentation of exogenous antigens [J].
Ackerman, AL ;
Cresswell, P .
NATURE IMMUNOLOGY, 2004, 5 (07) :678-684
[2]   EVIDENCE THAT TRANSPORTERS ASSOCIATED WITH ANTIGEN-PROCESSING TRANSLOCATE A MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I-BINDING PEPTIDE INTO THE ENDOPLASMIC-RETICULUM IN AN ATP-DEPENDENT MANNER [J].
ANDROLEWICZ, MJ ;
ANDERSON, KS ;
CRESSWELL, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (19) :9130-9134
[3]   Assembly and export of MHC class I peptide ligands [J].
Antoniou, AN ;
Powis, SJ ;
Elliott, T .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (01) :75-81
[4]   Stoichiometric tapasin interactions in the catalysis of major histocompatibility complex class I molecule assembly [J].
Bangia, N ;
Cresswell, P .
IMMUNOLOGY, 2005, 114 (03) :346-353
[5]  
Bangia N, 1999, EUR J IMMUNOL, V29, P1858, DOI 10.1002/(SICI)1521-4141(199906)29:06<1858::AID-IMMU1858>3.0.CO
[6]  
2-C
[7]   Tapasin-mediated retention and optimization of peptide ligands during the assembly of class I molecules [J].
Barnden, MJ ;
Purcell, AW ;
Gorman, JJ ;
McCluskey, J .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :322-330
[8]   HLA-DM, HLA-DO and tapasin:: functional similarities and differences [J].
Brocke, P ;
Garbi, N ;
Momburg, F ;
Hämmerling, GJ .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (01) :22-29
[9]   MINIMAL REQUIREMENTS FOR PEPTIDE MEDIATED ACTIVATION OF CD8(+) CTL [J].
BROWER, RC ;
ENGLAND, R ;
TAKESHITA, T ;
KOZLOWSKI, S ;
MARGULIES, DH ;
BERZOFSKY, JA ;
DELISI, C .
MOLECULAR IMMUNOLOGY, 1994, 31 (16) :1285-1293
[10]   PEPTIDE BINDING TO CLASS-I MHC ON LIVING CELLS AND QUANTITATION OF COMPLEXES REQUIRED FOR CTL LYSIS [J].
CHRISTINCK, ER ;
LUSCHER, MA ;
BARBER, BH ;
WILLIAMS, DB .
NATURE, 1991, 352 (6330) :67-70