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
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