T Cell Antigen Receptor Recognition of Antigen-Presenting Molecules

被引:565
作者
Rossjohn, Jamie [1 ,2 ,3 ]
Gras, Stephanie [1 ,2 ]
Miles, John J. [3 ,4 ,5 ]
Turner, Stephen J. [6 ]
Godfrey, Dale I. [6 ,7 ]
McCluskey, James [6 ]
机构
[1] Monash Univ, Sch Biomed Sci, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[2] Monash Univ, Australian Res Council, Ctr Excellence Adv Mol Imaging, Clayton, Vic 3800, Australia
[3] Cardiff Univ, Sch Med, Inst Infect & Immun, Cardiff CF14 4XN, S Glam, Wales
[4] QIMR Berghofer Med Res Inst, Brisbane, Qld 4006, Australia
[5] QIMR Berghofer Ctr Immunotherapy & Vaccine Dev, Brisbane, Qld 4006, Australia
[6] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[7] Univ Melbourne, Ctr Excellence Adv Mol Imaging, Australian Res Council, Parkville, Vic 3010, Australia
来源
ANNUAL REVIEW OF IMMUNOLOGY VOL 33 | 2015年 / 33卷
基金
澳大利亚研究理事会;
关键词
major histocompatibility complex; CD1; MR1; T cell antigen receptor; MAJOR HISTOCOMPATIBILITY COMPLEX; MHC CLASS-II; HUMAN-LEUKOCYTE ANTIGENS; VITAMIN-B METABOLITES; BULGED VIRAL PEPTIDE; HUMAN AUTOIMMUNE TCR; STRUCTURAL BASIS; CRYSTAL-STRUCTURE; CROSS-REACTIVITY; SELF-PEPTIDE;
D O I
10.1146/annurev-immunol-032414-112334
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Major Histocompatibility Complex (MHC) locus encodes classical MHC class I and MHC class II molecules and nonclassical MHC-I molecules. The architecture of these molecules is ideally suited to capture and present an array of peptide antigens (Ags). In addition, the CD1 family members and MR1 are MHC class I like molecules that bind lipid-based Ags and vitamin B precursors, respectively. These Ag-bound molecules are subsequently recognized by I cell antigen receptors (ICRs) expressed on the surface of Tlymphocytes. Structural and associated functional studies have been highly informative in providing insight into these interactions, which are crucial to immunity, and how they can lead to aberrant T cell reactivity. Investigators have determined over thirty unique TCR-peptide-MHC-II complex structures and twenty unique TCR-peptide-MHC-II complex structures. These investigations have shown a broad consensus in docking geometry and
引用
收藏
页码:169 / 200
页数:32
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